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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
SUMMARY OF JOB DUTIES:
With guidance from research management or more senior professionals, ensures that research activities in the section/group laboratories and associated operations are in compliance with the safety policies and programs of the company, as well as, local, state and federal regulations. With guidance from research management or more senior professionals, ensures that research activities in the section/group laboratories and associated operations are in compliance with the company's environmental policies and programs through execution of assigned responsibilities for reducing waste and promoting environmental protection. With guidance from research management or more senior professionals, plans and conducts experimental programs to complete a phase of a project or a number of projects of minor scope. Under close supervision, conducts research on and testing of improvement of existing products, development of new products and technology and may include routine to complex synthesis or testing.
Assignment maybe a phase of a major project or a total project of minor scope. With minimal supervision from more experienced professionals, conducts routine synthesis or testing which provide experience and familiarization with methods, practices and programs (analytical, performance, physical properties, etc.). Under the guidance of more senior professionals or research management, acquires knowledge of NALCO Champion products, procedures and applications. Interfaces with section personnel in trouble-shooting problems with hardware, testing/synthesis equipment, product and methods development. May be responsible for timely calibration and maintenance of the various laboratory and equipment and documentation according to the company's business processes. With minimal guidance, conducts literature searches and gathers pertinent information related to specific topics. Under minimal supervision, compile, analyze and correlate technical data and writes timely reports on projects completed or progress reports.
Writes procedures in accordance with the company's business practices. Works with research management to formulate goals aligned with the executive leadership's initiatives and for professional growth.
MINIMUM QUALIFICATIONS (special skills, knowledge, ability, education, etc.):
Requires a B.S.
in Chemistry or related technical field or can be progressed from Assist Chemist (performance-based and tested) Good communication (oral and written) skills. Proficiency in computer programs necessary for writing reports and performing mathematical calculations. Knowledge of specialized scientific programs for molecular structure drawing, experimental design and statistics is a plus. Must be able to work in the United States without sponsorship
Wage: 28.00 per hour.
This position is 12.5% annual bonus eligible.
Benefits, upon satisfaction of applicable eligibility requirements, include but are not limited to: medical, dental, vision, life insurance, disability, vacation, ETO, parental leave, 14 paid holidays, Personal Time off pay, 401(k) with company match, employee stock purchase plan, and pension plan.
Apply for this ad Online! ....Read more...
Type: Permanent Location: Corsicana, Texas
Posted: 2024-04-22 23:09:35
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JOB DESCRIPTION
The Continuous Improvement Leader will lead continuous improvement efforts at the manufacturing plant level.
They will work with plant management and personnel to maintain and improve the MS168 Continuous Improvement program.
They will also work with the manufacturing plants and various corporate functions to determine where the most significant areas of improvement exist.
Complete Six Sigma projects and provide support for plant level Six Sigma Projects.
In addition, they will organize and execute focused Improvement Teams (like Kaizen Events).
Responsibilities
Implement, develop, and sustain MS168 Continuous Improvement Program.
(Including Conducting Semi-Annual Audits) Complete Six Sigma projects and provide support for plant level Six Sigma projects. Work with the manufacturing plants and various corporate functions to determine where the most significant areas of improvement exist and develop projects from those opportunities. Organize and execute and track progress of Focused Improvement Teams Provide a Supportive Project Management Office including MPST & Monthly Savings tracking and reporting. Provide Training of Lean Manufacturing Principals and Six Sigma Tools to Plant and Corporate Associates Track Company Key Performance Indicators and develop action plans for identified areas of opportunity.
Requirements
5 years of experience in the manufacturing industry. 50% of the role is on floor and 50% in office. Should be willing to work with hourly associates and staff directly.
Should be willing to work on the floor, roll up their sleeves and be a part of the team. Engineering or Chemistry degree is preferred but not mandatory with good significant manufacturing experience, use of lean principles in daily work. Six Sigma Black Beltpreferred. Sealant, Adhesive, Coating or Paint industry experience preferred. Able to travel 50%. Technical Expertise: Strong root cause analysis skills.
Experience with processes such as TapRooT, Kepner Tregoe or equivalent is preferable. Demonstrated use of analytical analysis: statistical process control, process capability analysis, correlation, ANOVA, DOE preferable. Proficiency in Microsoft Office (Word, Excel and PowerPoint). Preferable proficiency in ERP Systems (SAP, Business Objects, etc.) and Statistical Analysis Software (Minitab, etc.) Knowledge of and demonstrated use of Lean Manufacturing tools. Leadership Skills: Must be self-motivated. Ability to motivate others. Ability to endorse and practice teamwork. Project Management Skills Project management experience required. Must be organized and committed to meeting deadlines. Possesses the skill to lead multiple improvement projects at the same time. Communication Skills: Able to speak, listen, and write well. Effective presenter, facilitator, and trainer. Proficiency in creating effective reports.
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 23:07:14
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JOB DESCRIPTION
Position Summary:
We are seeking a highly motivated and detail-oriented Chemist with 0-2 years of experience in the field of paint and coatings.
The ideal candidate will have a strong educational background in physical sciences, holding at least a bachelor's degree.
The position is based at DayGlo Color Corporation in Cleveland, OH, a subsidiary of RPM International, a global leader in specialty coatings, sealants, and building materials.
Responsibilities:
Pigment Dispersion: Execute and optimize the preparation of pigment dispersions for paint and coating formulations, ensuring quality and consistency.
Laboratory Work: Conduct experiments, analyses, and tests to support product development and improvement initiatives.
Documentation: Maintain accurate and detailed records of experimental procedures, results, and observations in accordance with industry standards.
Collaboration: Work closely with cross-functional teams, including researchers and engineers, to contribute to the overall success of projects.
Quality Control: Assist in quality control processes, ensuring compliance with industry regulations and DayGlo's high standards.
Research: Stay updated on industry trends, new technologies, and advancements in paint and coatings to contribute innovative ideas to the team.
Communication: Strong verbal and written communication skills to effectively convey findings and collaborate with team members.
Analytical Thinking: Ability to analyze data, troubleshoot issues, and propose effective solutions. Initiative: Proactive attitude towards learning and taking on new challenges. This is an exciting opportunity for an early-career chemist to contribute to cutting-edge projects at DayGlo Color Corporation, supported by the extensive resources and global presence of RPM International.
If you meet the qualifications and are eager to grow in your career, we invite you to apply.
Experience: 0-2 years of relevant experience in the paint and coatings industry, with a focus on pigment dispersion preparation.
Education: Minimum of a bachelor's degree in physical sciences, Chemistry, or a related field.
Technical Skills: Familiarity with laboratory techniques, equipment, and procedures.
Knowledge of formulation principles in the paint and coatings domain is a plus.Apply for this ad Online! ....Read more...
Type: Permanent Location: Cleveland, Ohio
Posted: 2024-04-22 23:07:10
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JOB DESCRIPTION
DAP is looking to hire Quality Engineer at our Corporate Office. The Quality Engineer works closely with Operations, R&D, Sales, Marketing, and Technical Customer Service to ensure that products manufactured in each of the plants consistently meet customer expectations at the lowest possible cost.
Maintain and continuously improve the DAP Quality Management System while developing our associates.
This position will be located at the DAP Corporate Office.
Responsibilities
Support DAP Quality Management System elements. Execute New Product Performance Program Testing, Analysis and Reporting. Perform Complaint Testing, Analysis, facilitate formal Root Cause Analysis, and Corrective Actions (CAPA). Participate in Plant Trials for New Product Commercialization. Oversee Routine Measurement System Analysis, Standardization of Testing & Calibration, scope & implement new testing methods / equipment. Work with various business functions to understand customer expectations and assure measurement reproduces the customer experience for effective performance measurement.
Requirements
2 + years of experience in similar technical background. Bachelor's degree in engineering or chemistry. Paint, Coating, Adhesive and Sealant industry experience preferred.
Knowledge and demonstrated application of industry standard Quality Management and Quality Engineering practices. Demonstrated application of Statistical Process Control and Process Capability Analysis.
Strong understanding and experience in application of analytical tools such as Gauge R&R Studies, Measurement Capability Studies, and Multivariate Testing/ Design of Experiment.
Experience with material testing and generally accepted laboratory practices.
Very strong problem-solving skills.
Ability to effectively communicate with all levels of the organization including manufacturing plants, technical and management personnel.
Strong written and verbal communication skills.
ASQ Six Sigma certifications are preferred.
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 23:06:59
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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: 2024-04-22 23:06:50
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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: 2024-04-22 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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Senior R&D Chemist - Birmingham - Chemical Manufacturing
About The Role / Company
Our client, an established Chemicals manufacturing company, are currently looking to recruit an experienced R&D Chemist with a strong interest and passion for Organic Chemistry.
Working within New Product Introduction, your main responsibility will be hands on organic synthesis at bench scale.
This role will work closely with all areas of the business including Chemical Engineers, Process Safety Team, Analytical Team, Sales & Marketing and Operations, therefore excellent written and verbal communication skills are essential
Senior R&D Chemist - Package Details
£35,000 to £45,000 DOE
Days Based Position (Monday to Friday)
25 Days Holiday + Statutory
Life Assurance & Access to Pension Scheme
Senior R&D Chemist - Requirements
Hold a 1st Class bachelor's degree in Chemical Engineering (Essential)
MSc or PhD level qualification in a relevant discipline would be highly desirable
Strong Project Management skills with a minimum of 3 years' scale up experience
Senior R&D Chemist - Responsibilities
Hands on organic synthesis of products at bench scale
Evaluate and cost initial customer enquiries
Develop robust processes suitable for scale up and to produce small scale samples for internal & external evaluation and to scale up to pilot plant and production
....Read more...
Type: Permanent Location: Birmingham, England
Start: ASAP
Duration: Permanent
Salary / Rate: £35000 - £45000.00 per annum
Posted: 2024-04-16 14:25:36
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Field Service Engineer
Sheffield
£40'000 - £43'000 + Bonuses + Overtime (OTE £55'000 Plus) + Technical Training + Private Healthcare + Holidays + Progression + Industry Leading Pension + Car / Van Option + Company Credit Card + ‘Immediate Start'
Work as a Field Service Engineer role for an industry leader working a hugely varied role where you can earn in excess of £55'000.
Receive specialist training to constantly improve your electrical & mechanical skills.
Have the chance to earn the company bonus and be recognised as a specialist in this multi billion pound industry.
This company is industry leaders within the measuring and analysis field and due to growth they need a Field Service Engineer to join their highly skilled team.
You'll get to progress technically and into senior positions, enjoy earning a fantastic package while working on the best equipment there is, and being constantly challenged.You Role As A Field Service Engineer Will Include:
* Field Service Engineer Role - Covering South West England / Some Further Travel Required
* Repairing / Commissioning A Variety Of Analytical Measuring Equipment
* Consistent Training Courses - Overseas Travel IncludedAs A Field Service Engineer You Will Have:
* Clean Driving Licence
* Chemistry Understanding
* Worked Within The Lab / Medical Industry / Worked OnMeasuring Equipment
* Experience - Science / Chemistry backgroundPlease Apply Or Call Charlie Auburn on 0203 813 7949Keywords: Field Service Engineer, Field Technician, Analytical Equipment, Weighing Equipment, Science, Chemistry, Technician, Medical, Scales, Avionics, Electro-Mechanical, Engineer, Sheffield, Doncaster, Derby,Mansfield, ....Read more...
Type: Permanent Location: Sheffield, England
Start: ASAP
Salary / Rate: £40000 - £42000 per annum + Overtime + Bonus + Progression
Posted: 2024-04-09 15:20:26
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Laboratory Assistant [Part-time]Location: West LondonSalary: CompetitiveHours: Full timeFibrisol Service Ltd, part of ICL Food Specialties, is a leading supplier of functional food ingredients, operating from its manufacturing site in West London.The position provides general support to the QHSE department such as the completion of laboratory work.
The post holder will report directly to the Senior Technical and QHSE Manager.The role will suit an enthusiastic, well-organised individual with good laboratory analytical skills.
Education to HND level in Food Science, Chemistry, or other related discipline, is desirable.This position will attract a competitive salary and benefit package.An initial one-year contract with the possibility to become a permanent role by mutual agreement.
Closing date: 30th of April 2024.To ApplyClick "Apply" to forward your CV ....Read more...
Type: Contract Location: Acton, England
Start: ASAP
Posted: 2024-04-05 12:26:44
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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
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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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A leading Chemical company are looking for a QC Analyst to join their team in the Durham area.
Salary and Benefits of QC Analyst
Salary up to £28,000
Permanent Role
Skills and Qualifications needed for QC Analyst
Awareness of GMP Standards
Chemistry Degree
2 Years Experience in a relevant role
Fine Chemistry / Pharmaceutical Experience
HPLC and GC Experience
Responsibilities of the QC Analyst
The role of QC Analyst consists of Plan and prioritises own work with guidance from Senior Analyst or Manager.
Report analytical results accurately and in a timely manner as dictated by internal and external customer requirements and to carry out minor analytical method development to improve analysis, including HPLC, GC, spectrophotometric techniques and titrations
Additional Responsibilities of the QC Analyst:
Maintain the flow of documents within the department ensuring they are complete, accurate and compliant with procedures or guidelines
Carry out basic equipment maintenance and calibration of laboratory equipment following approved methods and procedures on assigned pieces of equipment
Write and review SOPs, Work Instructions and testing procedures for raw materials, intermediates and finished products
Monitor and maintain stock levels of reagents and consumables
For more information and to apply for the role of QC Analyst direct, please click the link below! ....Read more...
Type: Permanent Location: County Durham, England
Start: ASAP
Salary / Rate: £24000.00 - £28000.00 per annum
Posted: 2024-04-03 11:32:46
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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
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Field Service Engineer
Sheffield
£33'000 - £42'000 + Bonuses + Overtime (OTE £50'000 Plus) + Technical Training + Private Healthcare + Holidays + Progression + Industry Leading Pension + Car / Van Option + Company Credit Card + ‘Immediate Start'
Break into a Field Service Engineer role for an industry leader working a hugely varied role.
Receive specialist training to constantly improve your electrical & mechanical skills.
Earn a terrific package where you can earn in excess of £50'000 through bonuses and overtime.
This company is industry leaders within the measuring and analysis field and due to growth they need a Field Service Engineer to join their highly skilled team.
You'll get to progress technically and into senior positions, enjoy earning a fantastic package while working on the best equipment there is, and being constantly challenged.
This role is best suited for a candidate with a background in Science / Chemistry looking to break into a field based role. You Role As A Field Service Engineer Will Include:
* Field Service Engineer Role - Covering South West England / Some Further Travel Required
* Repairing / Commissioning A Variety Of Analytical Measuring Equipment
* Consistent Training Courses - Overseas Travel IncludedAs A Field Service Engineer You Will Have:
* Clean Driving Licence
* A Higher Certificate / Qualification In Chemistry
* Worked Within The Lab / Medical Industry
* Experience - Science / Chemistry background Please Apply Or Call Charlie Auburn on 0203 813 7949 Keywords: Field Service Engineer, Field Technician, Analytical Equipment, Weighing Equipment, Science, Chemistry, Technician, Medical, Scales, Avionics, Electro-Mechanical, Engineer, Sheffield, Doncaster, Derby,Mansfield, ....Read more...
Type: Permanent Location: Sheffield, England
Start: ASAP
Salary / Rate: £33000 - £42000 per annum + OTE ( £50'000 )+ Fantastic Training
Posted: 2024-03-21 09:41:21
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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: 15/03/2024
Salary / Rate: Competitive
Posted: 2024-03-15 08:55:03
