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We are currently looking for a Electrochemist to join a leading Diagnostics company based in the Bedfordshire area.
As the Electrochemist you will be responsible for executing electrochemistry and sensor research and development activities.
KEY DUTIES AND RESPONSIBILITIES:
Your duties as the Electrochemist will be varied however the key duties and responsibilities are as follows:
1.
As the Electrochemist you have a comprehensive understanding of theoretical and practical electrochemistry and be able to apply this to making and testing of electrochemical sensors incorporating molecularly imprinted polymers.
They should be inventive and creative in their approach to solving problems.
2.
You will work on different projects, solving technical problems and lead day-to-day laboratory activities which include R&D, method development, quality control, and method development.
3.
You will apply your experience in impedimetric and voltametric sensors, microfluids, biosensors, surface functionalisation, diagnostic or surface plasmon resonance and contribute new ideas and solutions to improve processes.
4.
To support the company progressing in their late stages, you will interact regularly with internal teams, and external customers to deliver interdisciplinary research projects and customer orders.
ROLE REQUIREMENTS:
To be successful in your application to this exciting opportunity as the Electrochemist we are looking to identify the following on your profile and past history:
1.
Relevant degree in Electrochemistry, or a related subject (Chemistry, Biochemistry, Bioengineering).
Industry experience is desirable, but not essential.
2.
A working knowledge and practical experience with Electrochemistry which can be applied to the preparation and testing of electrochemical sensors.
Key Words: Electrochemistry | Electrochemist | Biosensors | Microfluids | Surface Functionalisation | Surface Plasmon Resonance | Polymer | Chemistry | Bioengineering | ISO | Diagnostic | Analytical
Hyper Recruitment Solutions Ltd (HRS) is an Equal Opportunities employer who are certified by Investors in People for talent development.
We therefore welcome applications for any interested parties who fulfil the role requirements for this position.
HRS is a company exclusively supporting the science and technology sectors, and is made up of a collaboration of recruitment professionals and scientists.
We look forward to helping you with your next career moves. ....Read more...
Type: Permanent Location: Bedfordshire,England
Start: 30/04/2024
Salary / Rate: £32000 - £40000 per annum
Posted: 2024-04-30 18:49:03
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We have an exciting opportunity for a Bioanalytical Scientist to join a fast-growing CRO based in the Cheshire area.
As a bioanalytical scientist, you will be primarily laboratory-based, working with the team to ensure that bioanalytical assays utilising LC-MS/MS or Ligand Binding technology are performed to a GLP/GCP standard and delivered within scheduled time frames.
The team work on a broad range of molecule types including small molecules, peptides, Oligonucleotides and Proteins.
You will be involved with the development and validation of the assays and will also use the assays to analyse samples from the company's clients studies.
KEY DUTIES AND RESPONSIBILITIES:
Your duties as the Bioanalytical Scientist will be varied however the key duties and responsibilities are as follows:
1.
You will be responsible for the development of quantitative and qualitative methods for the analyses of drugs and biomarkers within a GLP / GCP environment.
2.
As a Scientist within the Bioanalysis team you will be carrying out LCMS/MS and HPLC methods for analysing drug metabolites as well as applying these methods in clinical and pre-clinical studies.
3.
Your role will include preparing and planning studies and reports whilst working in compliance with GLP / GCP.
Additional responsibilities will include routine MS, UPLC and bioanalytical extraction as well as method development, method validation and troubleshooting.
4.
As the Senior Scientist, you will have additional responsibilities such as supervise and mentor more junior laboratory scientists as well as some responsibility with client interaction when required.
ROLE REQUIREMENTS:
To be successful in your application to this exciting opportunity as the Bioanalytical Scientist we are looking to identify the following on your profile and past history:
1.
Relevant degree in a Life Sciences related degree such as, but not limited to, Chemistry, Biochemistry and Biotechnology.
2.
Proven industry experience of working in a bioanalytical laboratory performing quantitative analysis and experience of sample extraction techniques for biological sample analysis.
3.
Practical experience working within a regulated GLP / GCP / GxP / GMP laboratory is also essential to your application.
Key Words: Biotechnology | GCP | GMP | GxP | Life Sciences | LCMS | HPLC | Bioanalytical | Scientist | Chromatography | Drug Development | CRO | Quality | Biological Matrix | Bioanalysis Senior Scientist
Hyper Recruitment Solutions Ltd (HRS) is an Equal Opportunities employer who are certified by Investors in People for talent development.
We therefore welcome applications for any interested parties who fulfil the role requirements for this position.
HRS is a company exclusively supporting the science and technology sectors, and is made up of a collaboration of recruitment professionals and scientists.
We look forward to helping you with your next career moves. ....Read more...
Type: Permanent Location: Cheshire,England
Start: 30/04/2024
Salary / Rate: Competitive
Posted: 2024-04-30 09:47:30
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We have an exciting new opportunity for a Study Manager Team Lead to join a leading international CRO based in the North Yorkshire area.
As the Study Manager Team Lead you will be responsible for directly line managing a team of Study Managers for regulatory and non-regulatory small molecule bioanalytical studies.
KEY DUTIES AND RESPONSIBILITIES:
Your duties as the Study Manager Team Lead will be varied however the key duties and responsibilities are as follows:
1.
As the Study Manager Team Lead you will directly line manage a team of study managers to ensure the successful execution of small molecule bioanalytical studies.
2.
You will collaborate with cross-functional teams, including sponsors and clients, to plan and coordinate study activities, acting as departmental lead for bioanalytical activities conducted on assigned studies.
3.
As the Study Manager Team Lead you will oversee LC-MS/MS method development and troubleshooting including reviewing protocols, study plans, SOPs or reports as required.
4.
You will document and complete any quality documentation (quality issue, CAPA, deviation, change control) as appropriate and within required time frames.
ROLE REQUIREMENTS:
To be successful in your application to this exciting opportunity as the Study Manager Team Lead we are looking to identify the following on your profile and past history:
1.
Hold a degree in a Chemistry based subject or equivalent (e.g.
Biochemistry)
2.
Proven industry experience in study management leading small molecule bioanalytical studies.
3.
A working knowledge and practical experience using LC-MS/MS.
Key Words: Small Molecule | Study Manager | Team Lead | Bioanalysis | GLP | GCP | Method Development | Validation | Sample Analysis | Regulatory Compliance | LC-MS/MS
Hyper Recruitment Solutions Ltd (HRS) is an Equal Opportunities employer who are certified by Investors in People for talent development.
We therefore welcome applications for any interested parties who fulfil the role requirements for this position.
HRS is a company exclusively supporting the science and technology sectors, and is made up of a collaboration of recruitment professionals and scientists.
We look forward to helping you with your next career moves. ....Read more...
Type: Permanent Location: North Yorkshire,England
Start: 30/04/2024
Salary / Rate: £45000 - £65000 per annum
Posted: 2024-04-30 09:42:02
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JOB DESCRIPTION
Formulate new prods as requested by Mkting, re-formulate current prod lines for improvement, + solve tech scale-up + manufacturing probs by commercializing new or existing tech to support revenue growth + corp profits.
Analyze org + inorg compounds to determine chem + phys properties, composition, structure, relationships, + reactions, utilizing chromatography, spectroscopy, + spectrophotometry techniques.
Maintain lab instruments to ensure proper working order + troubleshoot malfunctions as needed.
Dev, improve, + customize products, equipment, formulas, processes, + analytical methods.
Conduct quality control tests.
Direct, coordinate, + advise personnel in test procedures for analyzing components + phys properties of materials.
Formulate or optimize any coating product in a known technology to meet defined requirements.
Design + conduct feasibility + cost savings studies independently.
Compile + analyze test information to determine process or equipment operating efficiency + to diagnose malfunctions.
Confer with scientists + engineers to conduct analyses of research projects, interpret test results, or develop nonstandard tests.
Write technical papers + reports + prepare standards + specifications for processes, facilities, products, or tests.
Induce changes in composition of substances by introducing heat, light, energy, + chemical catalysts for quantitative and qualitative analysis.
Must have Bach in Chemistry, Materials Science or related field and 5 years real exp with coatings or polymer research, and the following skills (5 yrs exp): characterization skill for polymeric materials, including viscosity, molecular weight, rheology profile, or mech properties; structure-property relationships for designing new polymer materials; and safety protocols and handling hazardous and flammable materials.
Alternatively, may have a Master's in Chemistry, Materials Science or related field and 2 years real exp with coatings or polymer research, and the following skills (2 yrs exp): characterization skill for polymeric materials, including viscosity, molecular weight, rheology profile, or mech properties; structure-property relationships for designing new polymer materials; and safety protocols and handling hazardous and flammable materials.
Any suitable combination of education, training, or experience is acceptable.
Pre-employment background checks and drug screen apply.Apply for this ad Online! ....Read more...
Type: Permanent Location: Pleasant Prairie, Wisconsin
Posted: 2024-04-29 23:31:46
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JOB DESCRIPTION
DAP is looking to hire R&D Intern for Summer 2024.
Responsibilities:
The summer intern would work under mentorship of a senior scientist / Supervisor to perform collaborative research for development adhesives or repair products with unique and differentiated properties.
This R&D work will include: • Formulating raw materials into a functional product.• Analytical testing to understand raw materials, as well as formulated product properties.• Benchmarking and applications testing of formulated products for end-use performance prediction.
Requirements
Major: Chemical Engineering or Chemistry Sophomore, Junior, or Senior. General lab skills (weighing materials on benchtop scale, transferring liquids/solids from one container to another, adherence to lab safety rules). Some organic chemistry knowledge and understanding of solvents. Adept with hands-on work, home repair experience is a plus! Attention to details, inquisitive, good notes taker, desire to learn and grow.
About DAP
DAP is a market leading manufacturer, innovator and marketer of home repair and construction products including caulks, sealants, spray foam insulation, adhesives, and patch and repair products.
DAP is part of RPM International Inc., a $6.1 billion, multinational company with subsidiaries that are world leaders in specialty coatings, sealants, building materials and related services. You will find DAP products in the hands of professional painters, remodelers, builders, and do-it-yourselfers, and in 60,000 retail outlets, ranging from home centers and mass merchandisers to your local hardware, pro contractor channels and paint stores.
DAP's eight manufacturing and distribution facilities in the United States of America and Canada service North America and the world. At DAP, we hire the best people and give them a collaborative and rewarding work environment that empowers them to succeed! We support associates in continuous professional growth and collaborate on the steps it takes to get to the next level in their careers.
Our associates enjoy a comprehensive benefits package including 401(k) with company match, pension, paid parental leave, competitive health insurance rates, employee stock purchase plan, tuition reimbursement, free wellness programs and more! Learn more about DAP's history, culture and benefits at www.dap.com/careers/
DAP - On the job since 1865.Apply for this ad Online! ....Read more...
Type: Permanent Location: Baltimore, Maryland
Posted: 2024-04-29 23:07:20
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JOB DESCRIPTION
DAP is looking for R&D Intern for Summer 2024.
Job Responsibilities
The summer intern would work under mentorship of a senior scientist to perform collaborative research. Study effect of graphene on fire resistance of sealant, 2 wk.
Study effect of graphene on tensile strength of adhesive, 2 wk.
Study effect of graphene on dust resistance of joint compounds, 2 wk.
Study effect of graphene on crack resistance and adhesion of concrete, 2 wk.
Validate and optimize for the most feasible formula in terms of performances and cost, 3 wk.
Review, prepare for final presentation, 1 wk.
Requirements
Currently pursuing a bachelor's degree in chemistry, materials science, polymer science, or related discipline from an accredited institution with a total GPA of 3.0 or higher.
Completed a minimum of 4 semesters by the start of the internship.
Available to work the entirety of the 12-week summer internship program in 2024.
6-12 months of practical laboratory experience in polymers, chemical/polymer processing, advanced analytical and materials characterization.
Previous relevant intern experience or co-op with company or university.
Use of designed experiments and statistical analysis of experimental results.
Demonstrated scientific and technical acumen, with ability to make connections between science/technology and real-world concerns. Strong problem-solving skills. Ability to deal with the ambiguity as it relates to technical problems and experimentation.
Demonstrated scientific excellence as evidenced by publications and presentations.
Self-motivated and self-directed.
About DAP
DAP is a market leading manufacturer, innovator and marketer of home repair and construction products including caulks, sealants, spray foam insulation, adhesives, and patch and repair products.
DAP is part of RPM International Inc., a $6.1 billion, multinational company with subsidiaries that are world leaders in specialty coatings, sealants, building materials and related services. You will find DAP products in the hands of professional painters, remodelers, builders, and do-it-yourselfers, and in 60,000 retail outlets, ranging from home centers and mass merchandisers to your local hardware, pro contractor channels and paint stores.
DAP's eight manufacturing and distribution facilities in the United States of America and Canada service North America and the world. At DAP, we hire the best people and give them a collaborative and rewarding work environment that empowers them to succeed! We support associates in continuous professional growth and collaborate on the steps it takes to get to the next level in their careers.
Our associates enjoy a comprehensive benefits package including 401(k) with company match, pension, paid parental leave, competitive health insurance rates, employee stock purchase plan, tuition reimbursement, free wellness programs and more! Learn more about DAP's history, culture and benefits at www.dap.com/careers/
DAP - On the job since 1865.Apply for this ad Online! ....Read more...
Type: Permanent Location: Baltimore, Maryland
Posted: 2024-04-29 23:07:13
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As a member of our GNSS team, you will be at the forefront of driving our technology forward.
This role presents abundant prospects for professional advancement spanning research, product development, and software engineering realms.
Key Responsibilities:
Collaborate with the development team to propel the software lifecycle.
Assume ownership of novel research and development initiatives.
Deliver precise technical outcomes and adeptly communicate with both internal and external stakeholders.
Lead and engage in R&D endeavours aimed at enhancing existing products and pioneering new technologies.
Your Experience:
Profound expertise in GNSS measurement engine signal processing.
Strong analytical capabilities utilizing Matlab or equivalent tools.
Thorough comprehension of the complete GNSS signal-processing chain.
Familiarity with synthetic aperture processing and GNSS simulators.
Mastery of Agile development methodologies.
Understanding of Kalman filters and other probabilistic estimation techniques.
Knowledge of multi-sensor fusion techniques, including GNSS-INS tight and deep coupling.
Experience with RTK, PPP, and multi-constellation positioning.
....Read more...
Type: Permanent Location: Girton, England
Start: ASAP, company can provide a sponsorship
Duration: Permanent
Salary / Rate: £75000 - £100000 Per Annum None
Posted: 2024-04-28 13:05:13
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As a member of our GNSS team, you will be at the forefront of driving our technology forward.
This role presents abundant prospects for professional advancement spanning research, product development, and software engineering realms.
Key Responsibilities:
Collaborate with the development team to propel the software lifecycle.
Assume ownership of novel research and development initiatives.
Deliver precise technical outcomes and adeptly communicate with both internal and external stakeholders.
Lead and engage in R&D endeavours aimed at enhancing existing products and pioneering new technologies.
Your Experience:
Profound expertise in GNSS measurement engine signal processing.
Strong analytical capabilities utilizing Matlab or equivalent tools.
Thorough comprehension of the complete GNSS signal-processing chain.
Familiarity with synthetic aperture processing and GNSS simulators.
Mastery of Agile development methodologies.
Previous involvement in product development, encompassing requirements capture and test definition.
Understanding of Kalman filters and other probabilistic estimation techniques.
Knowledge of multi-sensor fusion techniques, including GNSS-INS tight and deep coupling.
Experience with RTK, PPP, and multi-constellation positioning.
....Read more...
Type: Permanent Location: Bristol, England
Start: ASAP, company can provide a sponsorship
Duration: Permanent
Salary / Rate: £80000 - £98000 Per Annum None
Posted: 2024-04-28 12:53:03
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We are currently looking for a Qualified Person to join a leading Pharmaceutical company based in the South Yorkshire area.
As the Qualified Person you will be responsible for batch release of Pharmaceuticals and contributing to the management of QMS.
KEY DUTIES AND RESPONSIBILITIES:
Your duties as the Qualified Person will be varied however the key duties and responsibilities are as follows:
1.
As the Qualified Person you will review and approve batch records, analytical data, and other documentation related to the manufacturing and testing of medicinal products.
2.
You will oversee the release of medicinal products for distribution, ensuring compliance with all relevant regulations and guidelines.
3.
As the Qualified Person you will participating in internal and external audits of the manufacturing facilities and quality systems.
Providing expertise and guidance on regulatory requirements and quality standards to internal teams.
4.
You will investigate and resolve quality issues and deviations related to manufacturing processes and materials.
ROLE REQUIREMENTS:
To be successful in your application to this exciting opportunity as the Qualified Person we are looking to identify the following on your profile and past history:
1.
Relevant degree in a Pharmacy, Chemistry or closely related discipline and qualified QP.
2.
Proven industry experience in Pharmaceutical Manufacturing, Quality Assurance and Regulatory Compliance.
3.
A working knowledge and practical experience with activities of quantitative and qualitative analyses of active substances and of the necessary testing and checking to ensure the quality of medicinal products.
Key Words: QP, Qualified Person, Quality, Quality Assurance, QA, GMP, Manufacturing, Pharmaceuticals, South Yorkshire.
Hyper Recruitment Solutions Ltd (HRS) is an Equal Opportunities employer who are certified by Investors in People for talent development.
We therefore welcome applications for any interested parties who fulfil the role requirements for this position.
HRS is a company exclusively supporting the science and technology sectors, and is made up of a collaboration of recruitment professionals and scientists.
We look forward to helping you with your next career moves. ....Read more...
Type: Permanent Location: South Yorkshire,England
Start: 24/04/2024
Salary / Rate: £90000 - £100000 per annum
Posted: 2024-04-24 11:31:03
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We are currently looking for a Qualified Person to join a leading Pharmaceutical company based in the Staffordshire area.
As the Qualified Person you will be responsible for batch release of Pharmaceuticals and contributing to the management of QMS.
KEY DUTIES AND RESPONSIBILITIES:
Your duties as the Qualified Person will be varied however the key duties and responsibilities are as follows:
1.
As the Qualified Person you will review and approve batch records, analytical data, and other documentation related to the manufacturing and testing of medicinal products.
2.
You will oversee the release of medicinal products for distribution, ensuring compliance with all relevant regulations and guidelines.
3.
As the Qualified Person you will participating in internal and external audits of the manufacturing facilities and quality systems.
Providing expertise and guidance on regulatory requirements and quality standards to internal teams.
4.
You will investigate and resolve quality issues and deviations related to manufacturing processes and materials.
ROLE REQUIREMENTS:
To be successful in your application to this exciting opportunity as the Qualified Person we are looking to identify the following on your profile and past history:
1.
Relevant degree in a Pharmacy, Chemistry or closely related discipline and qualified QP.
2.
Proven industry experience in Pharmaceutical Manufacturing, Quality Assurance and Regulatory Compliance.
3.
A working knowledge and practical experience with activities of quantitative and qualitative analyses of active substances and of the necessary testing and checking to ensure the quality of medicinal products.
Key Words: QP, Qualified Person, Quality, Quality Assurance, QA, GMP, Manufacturing, Pharmaceuticals, Staffordshire.
Hyper Recruitment Solutions Ltd (HRS) is an Equal Opportunities employer who are certified by Investors in People for talent development.
We therefore welcome applications for any interested parties who fulfil the role requirements for this position.
HRS is a company exclusively supporting the science and technology sectors, and is made up of a collaboration of recruitment professionals and scientists.
We look forward to helping you with your next career moves. ....Read more...
Type: Permanent Location: Staffordshire,England
Start: 24/04/2024
Salary / Rate: £90000 - £100000 per annum
Posted: 2024-04-24 11:24:15
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JOB DESCRIPTION
Formulate new prods as requested by Mkting, re-formulate current prod lines for improvement, + solve tech scale-up + manufacturing probs by commercializing new or existing tech to support revenue growth + corp profits.
Analyze org + inorg compounds to determine chem + phys properties, composition, structure, relationships, + reactions, utilizing chromatography, spectroscopy, + spectrophotometry techniques.
Maintain lab instruments to ensure proper working order + troubleshoot malfunctions as needed.
Dev, improve, + customize products, equipment, formulas, processes, + analytical methods.
Conduct quality control tests.
Direct, coordinate, + advise personnel in test procedures for analyzing components + phys properties of materials.
Formulate or optimize any coating product in a known technology to meet defined requirements.
Design + conduct feasibility + cost savings studies independently.
Compile + analyze test information to determine process or equipment operating efficiency + to diagnose malfunctions.
Confer with scientists + engineers to conduct analyses of research projects, interpret test results, or develop nonstandard tests.
Write technical papers + reports + prepare standards + specifications for processes, facilities, products, or tests.
Induce changes in composition of substances by introducing heat, light, energy, + chemical catalysts for quantitative and qualitative analysis.
Must have Bach in Chemistry, Materials Science or related field and 5 years real exp with coatings or polymer research, and the following skills (5 yrs exp): characterization skill for polymeric materials, including viscosity, molecular weight, rheology profile, or mech properties; structure-property relationships for designing new polymer materials; and safety protocols and handling hazardous and flammable materials.
Alternatively, may have a Master's in Chemistry, Materials Science or related field and 2 years real exp with coatings or polymer research, and the following skills (2 yrs exp): characterization skill for polymeric materials, including viscosity, molecular weight, rheology profile, or mech properties; structure-property relationships for designing new polymer materials; and safety protocols and handling hazardous and flammable materials.
Any suitable combination of education, training, or experience is acceptable.
Pre-employment background checks and drug screen apply.Apply for this ad Online! ....Read more...
Type: Permanent Location: Pleasant Prairie, Wisconsin
Posted: 2024-04-22 23:10:25
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JOB DESCRIPTION
GENERAL PURPOSE OF THE JOB:
*100% REMOTE / TELEWORK
* Division - Tremco CPG IT - Corporate We are seeking an experienced and skilled Data Engineer to join our team! We are looking for a candidate that thrives in a collaborative environment, is a self-starter, and is passionate about data.
Our data team is the foundation for data-driven business decisions and is leading the way for continued growth in innovative markets within the construction industry. On the Corporate Data team, the Data Engineer II's purpose is to design, develop, and maintain the company's data infrastructure, pipelines, and workflows.
They are responsible for merging predictive and prescriptive modeling to ensure it stays consistent with data flowing across the organization.
They work closely with data scientists, analysts, and other stakeholders to ensure the data is properly collected, stored, processed, and analyzed to drive informed business decisions. If you are passionate about data science and want to work with a dynamic team of professionals, please apply today!
ESSENTIAL DUTIES AND RESPONSIBILITIES:
Design, develop, build, and maintain the company's data infrastructure, pipelines, and workflows and all associated engineering tasks. Develop and maintain ELT processes to collect and integrate data from various sources. Build and maintain data APIs to enable data access across the organization. Develop and implement scalable data solutions to optimize data processing, storage, and retrieval. Develop and maintain documentation for data pipelines, including data dictionaries, standard operating procedures, and data flow diagrams. Work with unstructured data and develop data models to enable data analysis and insights. Identify any hidden patterns or data inconsistencies and work along with similar ad-hoc analysis Ensure data quality, consistency, and accuracy and is properly structured and formatted to support analyses. Ensure data security, integrity, and compliance with data privacy regulations. Troubleshoot and resolve data-related issues, including data quality, integrity, and performance. Continuously monitor, maintain, and optimize the health and performance of the data infrastructure, pipelines, and workflows Collaborate with data scientists, analysts, and other stakeholders to understand data requirements. Stay up to date with the latest advancements in data engineering and recommend new technologies, tools, and processes to improve efficiency and productivity.
EDUCATION:
Bachelor's or Master's degree in Information Technology, Computer Science, or a related field
EXPERIENCE:
3+ years of experience in a data science or related role
CERTIFICATES, LICENSES, REGISTRATIONS:
Not Required but beneficial: Certified SQL Certified SQL, Advanced Queries Python for Data Science & Machine Learning R for Data Science & Machine Learning Databricks Lakehouse Fundamentals
OTHER SKILLS AND ABILITIES:
Proficiency in programming languages such as Python, R, and SQL Strong understanding of database technologies and SQL queries Strong experience with ELT processes, data integration, and data modeling Experience with cloud-based data storage and computing services, specifically Azure Excellent problem-solving and analytical skills Experience with data visualization tools such as Tableau or Power BI Experience with data lakehouse tools such as Synapse (data lake) or databricks Excellent communication and collaboration skills Ability to work independently and prioritize tasks in a fast-paced & dynamic environment
The salary range for applicants in this position generally ranges between $79,000 and $99,000.
This range is an estimate, based on potential employee qualifications, operations, needs, and other considerations permitted by law. Benefits: Tremco offers a variety of benefits to its employees, including not limited to: health insurance, paid holidays, paid time off, 401(k) with company match, Company Pension Plan, Performance Based Commission, and continuing education.
Qualified applicants will receive consideration for employment without regard to their race, color, religion, national origin, sex, sexual orientation, gender identity, protected veteran status or disability.Apply for this ad Online! ....Read more...
Type: Permanent Location: Beachwood, Ohio
Posted: 2024-04-22 23:07:45
-
JOB DESCRIPTION
DAP is looking to hire R&D Intern for Summer 2024.
Responsibilities:
The summer intern would work under mentorship of a senior scientist / Supervisor to perform collaborative research for development adhesives or repair products with unique and differentiated properties.
This R&D work will include: • Formulating raw materials into a functional product.• Analytical testing to understand raw materials, as well as formulated product properties.• Benchmarking and applications testing of formulated products for end-use performance prediction.
Requirements
Major: Chemical Engineering or Chemistry Sophomore, Junior, or Senior. General lab skills (weighing materials on benchtop scale, transferring liquids/solids from one container to another, adherence to lab safety rules). Some organic chemistry knowledge and understanding of solvents. Adept with hands-on work, home repair experience is a plus! Attention to details, inquisitive, good notes taker, desire to learn and grow.
About DAP
DAP is a market leading manufacturer, innovator and marketer of home repair and construction products including caulks, sealants, spray foam insulation, adhesives, and patch and repair products.
DAP is part of RPM International Inc., a $6.1 billion, multinational company with subsidiaries that are world leaders in specialty coatings, sealants, building materials and related services. You will find DAP products in the hands of professional painters, remodelers, builders, and do-it-yourselfers, and in 60,000 retail outlets, ranging from home centers and mass merchandisers to your local hardware, pro contractor channels and paint stores.
DAP's eight manufacturing and distribution facilities in the United States of America and Canada service North America and the world. At DAP, we hire the best people and give them a collaborative and rewarding work environment that empowers them to succeed! We support associates in continuous professional growth and collaborate on the steps it takes to get to the next level in their careers.
Our associates enjoy a comprehensive benefits package including 401(k) with company match, pension, paid parental leave, competitive health insurance rates, employee stock purchase plan, tuition reimbursement, free wellness programs and more! Learn more about DAP's history, culture and benefits at www.dap.com/careers/
DAP - On the job since 1865.Apply for this ad Online! ....Read more...
Type: Permanent Location: Baltimore, Maryland
Posted: 2024-04-22 23:06:50
-
JOB DESCRIPTION
DAP is looking for R&D Intern for Summer 2024.
Job Responsibilities
The summer intern would work under mentorship of a senior scientist to perform collaborative research. Study effect of graphene on fire resistance of sealant, 2 wk.
Study effect of graphene on tensile strength of adhesive, 2 wk.
Study effect of graphene on dust resistance of joint compounds, 2 wk.
Study effect of graphene on crack resistance and adhesion of concrete, 2 wk.
Validate and optimize for the most feasible formula in terms of performances and cost, 3 wk.
Review, prepare for final presentation, 1 wk.
Requirements
Currently pursuing a bachelor's degree in chemistry, materials science, polymer science, or related discipline from an accredited institution with a total GPA of 3.0 or higher.
Completed a minimum of 4 semesters by the start of the internship.
Available to work the entirety of the 12-week summer internship program in 2024.
6-12 months of practical laboratory experience in polymers, chemical/polymer processing, advanced analytical and materials characterization.
Previous relevant intern experience or co-op with company or university.
Use of designed experiments and statistical analysis of experimental results.
Demonstrated scientific and technical acumen, with ability to make connections between science/technology and real-world concerns. Strong problem-solving skills. Ability to deal with the ambiguity as it relates to technical problems and experimentation.
Demonstrated scientific excellence as evidenced by publications and presentations.
Self-motivated and self-directed.
About DAP
DAP is a market leading manufacturer, innovator and marketer of home repair and construction products including caulks, sealants, spray foam insulation, adhesives, and patch and repair products.
DAP is part of RPM International Inc., a $6.1 billion, multinational company with subsidiaries that are world leaders in specialty coatings, sealants, building materials and related services. You will find DAP products in the hands of professional painters, remodelers, builders, and do-it-yourselfers, and in 60,000 retail outlets, ranging from home centers and mass merchandisers to your local hardware, pro contractor channels and paint stores.
DAP's eight manufacturing and distribution facilities in the United States of America and Canada service North America and the world. At DAP, we hire the best people and give them a collaborative and rewarding work environment that empowers them to succeed! We support associates in continuous professional growth and collaborate on the steps it takes to get to the next level in their careers.
Our associates enjoy a comprehensive benefits package including 401(k) with company match, pension, paid parental leave, competitive health insurance rates, employee stock purchase plan, tuition reimbursement, free wellness programs and more! Learn more about DAP's history, culture and benefits at www.dap.com/careers/
DAP - On the job since 1865.Apply for this ad Online! ....Read more...
Type: Permanent Location: Baltimore, Maryland
Posted: 2024-04-22 23:06:43
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We are currently looking for a Senior Analytical Development Scientist to join a leading developing Gene Therapy company based in London.
As the Senior Analytical Development Scientist you will be responsible for the driving the development of analytical assays for AAV product and process characterisation.
This opportunity would suit a Scientist with subject matter expertise in HPLC and other chromatography based analytical techniques, who also has experience analysing protein based products to support the hiring company's transition from pre-clinical and early stage to trials and commercial launch of products.
KEY DUTIES AND RESPONSIBILITIES:
Your duties as the Senior Analytical Development Scientist will be varied however the key duties and responsibilities are as follows:
1.
You will Develop and deliver HPLC based methods for AAV product and process characterisation.
Methods of interest include but are not limited to, HPCE, cIEF, CE-SDS, MS and LCMS for large molecule characterisation.
2.
You will manage projects, supporting and up-skilling Analytical Scientists within the team, and apply industry knowledge to scope new technologies applicable for AAV product and process characterisation.
3.
You will Tech Transfer to external manufacturing partners, work closely with the CMC team and support process analytical activities to support process development, as well as R&D teams focused on new technology development.
4.
You will support the regulatory team in providing SME analytical guidance, design and write experimental plans, and ensure data is handled accordingly to strict guidelines.
ROLE REQUIREMENTS:
To be successful in your application to this exciting opportunity as the Senior Analytical Development Scientist we are looking to identify the following on your profile and past history:
1.
Relevant degree in a Biochemistry, Biochemical Engineering degree or relevant.
A PhD is not required but advantageous.
2.
Proven industry experience where you have used Chromatography based techniques as an analytical tool for the assessment of Large Molecules.
Experience of method development and troubleshooting analytical assays is highly beneficial to this role.
3.
A working knowledge and practical experience working with AAV gene therapy within a GMP analytical testing environment.
Key Words: Analytical Development | Method Development | Assay Development | MDV | Protein Characterisation | Product Characterisation | Protein Analysis | AAV | Viral Vector | Gene Therapy | GMP | QC | Quality Control | CMC | Biologics | Biopharmaceutical | C> | ATMP
Hyper Recruitment Solutions Ltd (HRS) is an Equal Opportunities employer who are certified by Investors in People for talent development.
We therefore welcome applications for any interested parties who fulfil the role requirements for this position.
HRS is a company exclusively supporting the science and technology sectors, and is made up of a collaboration of recruitment professionals and scientists.
We look forward to helping you with your next career moves. ....Read more...
Type: Permanent Location: London,England
Start: 19/04/2024
Salary / Rate: Competitive
Posted: 2024-04-19 16:47:02
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Principal Scientist - Protein Engineering - Cambridge, MA
Newton Colmore is partnered with a biotech company in Cambridge MA, and we are searching for a principal-level scientist with expertise in protein engineering.
As a Principal Scientist within this organisation, you will be utilising your expertise to design and execute protein engineering strategies, design and develop new assays for kinetic and stability characterisation and to transfer results from early-stage concept into manufacture-ready developments across multiple therapeutic areas.
You will be part of a tight-knit team, multidisciplinary in nature, all working towards the goal of achieving a step-change in this technology.
To be considered for this exciting role we are looking for scientists with the following attributes;
Hands-on commercial experience in protein engineering.
Expertise with analytical techniques and computational approaches to protein engineering.
Ideally educated to PhD level in molecular biology or biochemistry
Industrial experience with assay development, high-throughput screening and enzyme characterization would be ideal.
In exchange for your skills and expertise, the company offer a highly competitive package and the chance to bring the technology to life.
For more information, make a confidential application now and a member of our team will be in touch with more details.
Newton Colmore is a specialist recruiter operating within the medical devices and biotechnology sectors.
We have over ten years worth of expertise of placing candidates with our clients, globally.
Our sole aim is to utilise this expertise and knowledge to maximise your chances of securing your ideal role with our clients.
....Read more...
Type: Permanent Location: Cambridge, Massachusetts
Salary / Rate: Tailored package + bonus
Posted: 2024-04-17 11:34:30
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Head of Data Engineering
The Head of Data will be a strategic leader responsible for overseeing all aspects of data management, analytics, and governance within the organisation.
This individual will play a critical role in driving data-driven decision-making processes, optimising data infrastructure, and ensuring the integrity, security, and accessibility of data assets.
The ideal candidate will possess strong leadership skills, deep technical expertise in data management and analytics, and a proven track record of implementing innovative data strategies to support business objectives.
Key Responsibilities:
Strategic Leadership: Lead the development and execution of the organisation's data strategy, aligning it with business goals and objectives.
Provide strategic direction for the use of data to drive decision-making and improve operational efficiency.
Data Management: Oversee the design, implementation, and maintenance of robust data management systems and processes, including data acquisition, storage, integration, quality assurance, and lifecycle management.
Data Analytics: Drive the development and implementation of advanced analytics initiatives to extract insights from data, identify trends, and support predictive modelling and forecasting.
Collaborate with business stakeholders to understand their analytical needs and develop solutions to address them.
Data Governance: Establish and enforce data governance policies, standards, and best practices to ensure the accuracy, consistency, security, and privacy of data across the organization.
Develop data quality metrics and monitor compliance with regulatory requirements.
Data Architecture: Define and maintain the organization's data architecture, including data models, schemas, and taxonomies.
Evaluate and select appropriate technologies and tools to support data management, analytics, and visualization requirements.
Team Leadership: Build and lead a high-performing team of data professionals, including data engineers, analysts, scientists, and governance specialists.
Provide mentorship, coaching, and professional development opportunities to foster a culture of continuous learning and growth.
Cross-Functional Collaboration: Collaborate closely with other departments, including IT, finance, marketing, operations, and product development, to understand their data needs and priorities.
Partner with business leaders to develop data-driven solutions that drive value and competitive advantage.
Vendor Management: Evaluate and manage relationships with third-party data vendors, software providers, and consultants to ensure the successful implementation of data-related projects and initiatives.
Negotiate contracts, oversee vendor performance, and assess emerging technologies and trends in the data management space.
Qualifications:
Bachelor's degree in computer science, engineering, mathematics, statistics, or a related field; advanced degree (e.g., MBA, MS, or PhD) preferred.
10+ years of experience in data management, analytics, and business intelligence, with at least 5 years in a leadership role.
Proven track record of developing and implementing data strategies that drive business growth and innovation.
Deep understanding of data governance principles, regulatory compliance requirements (e.g., GDPR, CCPA), and industry best practices.
Strong technical proficiency in data modelling, SQL, ETL tools, data visualization tools (e.g., Tableau, Power BI), and advanced analytics techniques (e.g., machine learning, predictive modelling).
Excellent leadership, communication, and interpersonal skills, with the ability to influence and collaborate effectively across all levels of the organization.
Demonstrated experience in managing cross-functional teams and driving cultural change towards a data-driven mindset.
Ability to thrive in a fast-paced, dynamic environment and effectively prioritize and manage multiple projects and initiatives.
Interested? Please submit your updated CV to Lucy Morgan at Crimson for immediate consideration.
Not interested? Do you know someone who might be a perfect fit for this role? Refer a friend and earn £250 worth of vouchers!
Crimson is acting as an employment agency regarding this vacancy.
Please see our website for Crimson's Privacy Statement, should you wish to view prior to applying for this vacancy.
....Read more...
Type: Permanent Location: Ashford, England
Salary / Rate: £80000 - £90000 per annum
Posted: 2024-04-11 16:37:28
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Are you a Biomedical Scientist seeking a new challenge? Do you have a passion for biochemistry?Service Care Solutions are working with East Lancashire Hospitals NHS Foundation Trust to recruit a Band 6 Biomedical Scientist to support a Biochemistry Haematology Team in the Lancashire area.
The post entails analytical investigation, and confirmation of the analytical and technical validity of those investigations, liaising with clinical and blood science staff to ensure diagnostically abnormal results are urgently acted upon.The contract duration is for 4 months with the likelihood of extension.
This is a full-time placement with 37.5 hours available.
Part-time applications of 3 Days or more will also be considered.
Shifts: 37.5 hours on a 24/7 rotaLocation: East LancashirePay: £25.00 p/h LTDBonus: £250 Sign-Up BonusJob Purpose - Band 6 Specialist Biomedical Scientist - Biochemistry / HaematologyKey Responsibilities
Perform a wide array of routine and specialised analyses swiftly, ensuring accuracy and efficiency in service delivery.
Demonstrate the ability to conduct investigations and utilize various analytical techniques independently, while effectively organizing tasks under the guidance of a Senior Biomedical Scientist.
Fulfil the requirement to rotate through all department sections, including specimen reception, to gain comprehensive experience and understanding.
Adhere strictly to approved Standard Operating Procedures within the Department to maintain consistency and quality in analytical processes.
Actively contribute to the development of Standard Operating Procedures, offering valuable insights and recommendations for enhancements and amendments when necessary.
Execute intricate manual and automated analytical investigations, drawing upon specialized skills and expertise.
Operate sophisticated, high-value analytical equipment with confidence and precision, ensuring seamless workflow and accurate results without supervision.
Take responsibility for the maintenance, troubleshooting, and repair of complex laboratory instruments, ensuring uninterrupted essential services in the event of technical failures.
Prepare reagents, control materials, and calibrators with utmost precision and accuracy, essential for maintaining the integrity of analytical processes and results.
Handle hazardous and noxious chemicals safely and effectively, while also managing frequent exposure to uncontained bodily substances, adhering strictly to safety protocols and procedures.
Requirements
IBMS Accredited degree
HCPC Registration
Completed / Working towards specialist IBMS portfolio
Biochemistry / haematology Experience
Benefits
Four weekly payroll runs
£250 training allowance
Excellent pay rates
Exceptional referral bonuses
Frequent notifications for upcoming opportunities via text and email
Ltd & PAYE payment options available
FREE DBS disclosures provided via fast track online services
FREE Occupational Health Check and Immunisations
£150 Agency Switch Bonus
£250 Welcome Bonus
Up to £750 Referral Bonus
....Read more...
Type: Contract Location: Blackburn, England
Start: ASAP
Salary / Rate: Up to £25.00 per hour + £250 bonus
Posted: 2024-04-04 13:39:23
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We are looking for a Senior Data Engineer to join our client's Data Analytics & AI Team, where you will play a key role in constructing and automating the infrastructure of our data and AI platform and developing functional data components.
Working in collaboration with our business unit platform teams, you'll be responsible for designing, building, and managing the infrastructure and tools that enable efficient processing and analysis of large data sets to support successful running of AI projects.
Requirements:
Bachelor's or Master's degree in Computer Science, Data Science, or a related field.
Advanced Python knowledge for data processing and scripting.
Hands-on experience with one or more cloud services (Azure, AWS, GCP).
Proficiency in SQL and NoSQL databases.
Experience with Data as Code; version control, small and regular commits, unit tests, CI/CD, packaging, familiarity with containerization tools such as Docker and Kubernetes.
Experience with Infrastructure as Code is a plus.
Strong problem-solving skills and attention to detail.
Good communication skills, fluent English.
Responsibilities:
Develop and maintain scalable data pipelines.
Create efficient Extract, Transform, Load (ETL) processes to handle data transformation and preparation.
Ensure data accuracy and integrity across various sources.
Work with data warehousing technologies to organize and store large volumes of data.
Optimize data storage and retrieval for analytical and operational purposes.
Collaborate with data scientists to deploy machine learning models (incl.
LLMs) into production environments.
Leverage tools like Kubeflow, MLflow to streamline the end-to-end ML lifecycle.
Ensure seamless integration of ML models with data pipelines.
Collaborate with business teams to enhance data models that feed business intelligence tools.
Foster data-driven decision-making by making data accessible to relevant stakeholders.
Implement software and methodologies for data correction, reconciliation, and quality checking.
Maintain data consistency across different data sources.
If interested, please get in touch via contact details provided or click “Apply” to forward an up-to-date copy of your CV.
Cavendish (Recruitment) Professionals Ltd are proud to be an equal opportunity employer and we believe that inclusivity begins with the candidate experience.
All qualified applicants will receive consideration for employment regardless of, gender, race, age, sexual orientation, religion, or belief. ....Read more...
Type: Contract Location: Prague, Czech Republic
Start: ASAP
Salary / Rate: Additional Benefits
Posted: 2024-04-03 17:49:16
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Are you an experienced Validation Specialist looking for a new exciting job opportunity?
We are currently looking for a Validation Specialist to join a leading pharmaceutical company based in the Caerphilly area.
As the Validation Specialist you will enhance validation practice and compliance; support improvement to validation system; streamline processes.
Identify risk areas and required mitigation to meet regulatory inspections e.g.
MHRA, FDA, Notified Body etc.
through routine compliance activities and specific validation projects.
KEY DUTIES AND RESPONSIBILITIES:
Your duties as the Validation Specialist will be varied however the key duties and responsibilities are as follows:
1.
You will be responsible for ensuring that the Site Validation Master Plan is maintained accurately and Validation Plans are implemented for all relevant aspects of Equipment, Process, Cleaning, Computer Systems, Facilities/Utilities and Analytical Method validation.
2.
Additionally, you will also be assisting with all validation activities on equipment before handover / return to system owner and updating all relevant records and schedules.
You will be responsible for arranging specialist services to maintain, calibrate and qualify specialist equipment.
3.
Technical input into all Validation Lifecycle activities as part of a cross functional team.
Provide guidance and support to other internal site departments ensuring compliance with applicable regulatory requirements (MHRA, EU, FDA, U.S., Notified Body and international), International Standards, and quality/validation regulations and guidance documents.
4.
You will also prepare and present validation reports and Key Performance Indicators for management review.
Review and monitor trends; initiate continuous improvement opportunities, communicate any matters outside the norm to the Validation Manager / Site Director of Quality.
ROLE REQUIREMENTS:
To be successful in your application to this exciting opportunity as the Validation Specialist we are looking to identify the following on your profile and past history:
1.
Successful validation experience in a GMP environment (in the pharmaceutical, medical devices, consumer healthcare or semi-conductor industry) is essential for this position.
Experience working in a sterile manufacturing facility would be highly desirable.
2.
Demonstrated expertise in cGMP's, EU/FDA regulations, GAMP guidelines, assessment of risk and drafting of plans, protocols, reports and procedures.
3.
Previous team leadership experience (direct or indirect) desirable, operating in a matrix organization.
Key Words: Validation Specialist | Validation Engineer | Biotechnology | Life Science | Pharmaceutical | GMP | Manufacturing | Sterile Cleanroom | Quality Assurance
Hyper Recruitment Solutions Ltd (HRS) is an Equal Opportunities employer who are certified by Investors in People for talent development.
We therefore welcome applications for any interested parties who fulfil the role requirements for this position.
HRS is a company exclusively supporting the science and technology sectors, and is made up of a collaboration of recruitment professionals and scientists.
We look forward to helping you with your next career moves. ....Read more...
Type: Permanent Location: Caerphilly,Wales
Start: 27/03/2024
Salary / Rate: Dependent on experience
Posted: 2024-03-27 11:05:09
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Algorithm Scientist/Data Analyst/Mathematician/Maths Modelling scientist/engineer detail-oriented individual with a strong analytical mindsetData Scientist/Data Analyst will have excellent working experience if python or matlab or C++Good qualifications in Maths or Physics or Computer Science or Physical scienceStrong analytical, mathematical, and problem-solving skillsDemonstrable accuracy and attention to detailAbility to analyse and interpret numerical data through statistical analysis, modelling, and optimisation techniques.
As a supply hero with rTriibe
Numerical data analysis to obtain relevant information for the project
Strong computer fundamentals such as Excel, VBA, SQL or Python experience preferredWillingness to learn additional skills such as PySpark and Data ModellingSome understanding of data visualisation and/or wider user interface design an advantage
....Read more...
Type: Permanent Location: Cheltenham, England
Start: asap
Salary / Rate: £30000 - £50000 per annum
Posted: 2024-03-26 18:10:29
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We are currently looking for a QC Analyst to join a leading company based in the Kent area.
As the QC Analyst you will be responsible for the analysis of pharmaceutical raw materials, APIs, and finished products to ensure compliance with internal and regulatory specifications.
Daily tasks will involve general chemical analysis including stability testing, various laboratory support activities, documenting analytical data, writing reports and SOPs all in accordance with cGMP.
KEY DUTIES AND RESPONSIBILITIES:
Your duties as the QC Analyst will be varied however the key duties and responsibilities are as follows:
1.
As a QC Analyst you will be involved in Performing analytical testing using GC, HPLC, KF, FTIR and other required techniques in accordance with written procedures.
2.
You will be required to record data into appropriate records and notify the line manager of any OOS, OOT, OOE or questionable results
3.
You will create and update documents in accordance with cGMP and company procedures
ROLE REQUIREMENTS:
To be successful in your application to this exciting opportunity as the QC Analyst we are looking to identify the following on your profile and past history:
1.
Relevant degree in a chemistry or related science discipline.
2.
Proven industry experience in Pharmaceutical QC testing and GMP (ideally small molecule) and analytical testing using GC, HPLC, KF, FTIR.
3.
Experience in completing OOS investigations, deviations, CAPA, and Change Controls
Key Words: GC / HPLC / TLC / FTIR / QC / Quality Control/ QC Scientist/ GMP / API / Raw materials / Chemistry / analytical /
Hyper Recruitment Solutions Ltd (HRS) is an Equal Opportunities employer who are certified by Investors in People for talent development.
We therefore welcome applications for any interested parties who fulfil the role requirements for this position.
HRS is a company exclusively supporting the science and technology sectors, and is made up of a collaboration of recruitment professionals and scientists.
We look forward to helping you with your next career moves. ....Read more...
Type: Permanent Location: Kent,England
Start: 25/03/2024
Salary / Rate: £27000 - £29000 per annum
Posted: 2024-03-25 14:32:15
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We have an exciting new opportunity for a Study Manager Team Lead to join a leading international CRO based in the North Yorkshire area.
As the Study Manager Team Lead you will be responsible for directly line managing a team of Study Managers for regulatory and non-regulatory small molecule bioanalytical studies.
KEY DUTIES AND RESPONSIBILITIES:
Your duties as the Study Manager Team Lead will be varied however the key duties and responsibilities are as follows:
1.
As the Study Manager Team Lead you will directly line manage a team of study managers to ensure the successful execution of small molecule bioanalytical studies.
2.
You will collaborate with cross-functional teams, including sponsors and clients, to plan and coordinate study activities, acting as departmental lead for bioanalytical activities conducted on assigned studies.
3.
As the Study Manager Team Lead you will oversee LC-MS/MS method development and troubleshooting including reviewing protocols, study plans, SOPs or reports as required.
4.
You will document and complete any quality documentation (quality issue, CAPA, deviation, change control) as appropriate and within required time frames.
ROLE REQUIREMENTS:
To be successful in your application to this exciting opportunity as the Study Manager Team Lead we are looking to identify the following on your profile and past history:
1.
Hold a degree in a Chemistry based subject or equivalent (e.g.
Biochemistry)
2.
Proven industry experience in study management leading small molecule bioanalytical studies.
3.
A working knowledge and practical experience using LC-MS/MS.
Key Words: Small Molecule | Study Manager | Team Lead | Bioanalysis | GLP | GCP | Method Development | Validation | Sample Analysis | Regulatory Compliance | LC-MS/MS
Hyper Recruitment Solutions Ltd (HRS) is an Equal Opportunities employer who are certified by Investors in People for talent development.
We therefore welcome applications for any interested parties who fulfil the role requirements for this position.
HRS is a company exclusively supporting the science and technology sectors, and is made up of a collaboration of recruitment professionals and scientists.
We look forward to helping you with your next career moves. ....Read more...
Type: Permanent Location: North Yorkshire,England
Start: 25/03/2024
Salary / Rate: £45000 - £60000 per annum
Posted: 2024-03-25 09:44:03
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We are currently looking for a GLP Study Director to join a leading CRO company based in the Oxfordshire area.
As the GLP Study Director you will be responsible for overseeing GLP studies, executing sample preparation for analysis using various techniques and tools, and collaborating closely with the Laboratory Manager and team to ensure timely project delivery.
KEY DUTIES AND RESPONSIBILITIES:
Your duties as the GLP Study Director will be varied however the key duties and responsibilities are as follows:
1.
To apply your experience using chromatographic techniques using HPLC, IC,GC and LC for the analysis of various analytical samples.
2.
Conducting the design of study plans, method validation, method development and to ensure timely project delivery, setting and maintaining high personal standards for study quality.
3.
Oversee GLP studies in strict adherence to guidelines, ensuring compliance with standard operating procedures, and maintaining accurate data records.
4.
Taking an active role in the up-skilling and supervision of Analysts whilst effectively communicating with management to ensure the constant development of the overall Analytical function / team.
ROLE REQUIREMENTS:
To be successful in your application to this exciting opportunity as the GLP Study Director we are looking to identify the following on your profile and past history:
1.
Relevant degree in Analytical Chemistry OR relevant disciplines
2.
Proven industry experience in working in a CRO GLP environment.
Experience working across agrochemical, biocide, industrial chemical and animal health industries is advantageous
3.
A working knowledge and practical experience with chromatographic techniques such as HPLC, IC, GC, LC.
Key Words: Analytical Chemistry | GLP Studies | Laboratory Equipment | Sample Preparation | Chromatographic Techniques | Project Delivery | Standard Operating Procedures | Data Records | Calibration | Preventive Maintenance | SOP | Study Director | Method Validation | Method Development | CRO | HPLC | LC | GC | Oxfordshire
Hyper Recruitment Solutions Ltd (HRS) is an Equal Opportunities employer who are certified by Investors in People for talent development.
We therefore welcome applications for any interested parties who fulfil the role requirements for this position.
HRS is a company exclusively supporting the science and technology sectors, and is made up of a collaboration of recruitment professionals and scientists.
We look forward to helping you with your next career moves. ....Read more...
Type: Permanent Location: Oxfordshire,England
Start: 25/03/2024
Salary / Rate: Competitive
Posted: 2024-03-25 09:36:08
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Post-Doctoral Researcher Chemist (Battery Materials)
Location: Godmanchester, Cambridgeshire
Salary: £39,000 + Excellent Benefits
Job Type: Full Time, Permanent
The Client:
Our client, a leading firm focused on accelerating research translation into marketable products.
The Role:
As a Post-Doctoral Researcher Chemist, you will contribute to developing energy storage materials, characterising and testing novel materials for batteries within a multidisciplinary team.
Duties:
* Contribute creatively to brainstorming sessions, studies, and project meetings.
* Assist in formulating electrode and electrolyte material inks and pastes, including solvent screening and microscopy studies.
* Characterize battery materials using electrochemical analysis techniques, including EIS.
* Fabricate and test coin cell devices with novel battery materials, interpreting data and making recommendations.
* Accurately record practical work to document new Intellectual Property (IP) and contribute to patent drafts.
* Initiate, deliver, and document high-quality studies to achieve R&D targets.
* Ensure compliance with health, safety, and environmental policies.
* Foster key working relationships with line managers, project teams, device scientists, and external partners.
* Coordinate activities and disseminate results with relevant teams.
Requirements:
Essential:
* PhD in chemistry, material science, physics, or related field, or equivalent industrial/academic experience.
* Strong knowledge and practical experience in electrochemical techniques or battery technologies.
* Familiarity with Windows and Microsoft Office.
Desirable:
* Experience in high-tech R&D or manufacturing.
* Additional background in organic, inorganic, or interface chemistry, and relevant analytical techniques.
* Understanding of structure-property relationships in functional materials.
* Interest in synthesis and evaluation of functional materials in device formats.
* Experience with Intellectual Property (IP) generation and patent filing.
Benefits:
* Competitive Salary
* Pension scheme
* 27 days holiday plus bank holidays
* Paid time off for voluntary work
* Employee Assistance Programme
* Flexi-time scheme and work-from-home opportunities
* Private health and dental care, life assurance, income protection insurance
Apply now for this exceptional opportunity to contribute to cutting-edge research and further enhance your career.
Important Information: We endeavour to process your personal data in a fair and transparent manner.
In applying for this role, Additional Resources will be acting in your best interest and may contact you in relation to the role, either by email, phone or text message.
For more information see our Privacy Policy on our website.
It is important you are aware of your individual rights and the provisions the company has put in place to protect your data.
If you would like further information on the policy or GDPR please contact us.
Additional Resources Ltd is an Employment Business and an Employment Agency as defined within The Conduct of Employment Agencies & Employment Businesses Regulations 2003.
Keywords: Materials Scientist, Research Scientist, Scientist, Battery Materials, Battery Technology, Battery
....Read more...
Type: Permanent Location: Godmanchester, England
Start:
Duration:
Salary / Rate: £39000 - £39000 Per Annum
Posted: 2024-03-22 17:11:33
