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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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The Company:
Regional Clinical Trainer
A market leading manufacturer and distributor of medical products.
Seeing continual and exponential growth.
A fantastic career opportunity.
The Role of the Regional Clinical Trainer:
Providing training and clinical support to nurses and other clinicians on an exciting new portfolio of IV access devices.
You will be liaising with theatre managers, sisters, nurses, neonatal departments, ITU/CCU/ICU, A&E
Working from home, visiting hospitals across the Midlands.
Responsible for influencing stakeholders and ensuring trials and training leads to positive customer experiences and outcomes.
Will be a lot of demo style short sessions in hospitals and some stand up face to face sessions that the successful candidate will deliver.
Benefits of the Regional Clinical Trainer:
£35k-£37k basic salary
£10k bonus
Car allowance £550 per month
Business mileage paid
Phone
Laptop
25 days holiday
Life assurance
Pension.
The Ideal Person for the Regional Clinical Trainer:
Amazing opportunity for someone that wants to join a good company that rewards people.
Ideally looking for someone with a little commercial experience, maybe a year as a nurse advisor with some training experience – either training patients or other nurses.
Must have some exposure to IV/Vascular Access/Venepuncture.
Registered as a nurse, Active PIN.
Highly motivated person, the role is challenging, exciting and rewarding.
Big preference for commercial experience but not definitely essential.
Must be au fait with IT packages such as Excel, PowerPoint etc.
Must be happy driving, it’s a big region and there will be plenty of overnight stays.
If you think the role of Regional Clinical Trainer is for you, apply now!
Consultant: Rio Barclay
Email: riob@otrsales.co.uk
Tel no.
0208 397 4114
Candidates must be eligible to work and live in the UK.
About On Target
At On Target, we specialise in sales, technical and commercial jobs in the Engineering, Construction, Building Services, Medical & Scientific, and Commercial & Industrial Solutions sectors, enabling our consultants to become experts in their market sector.
We place all levels of personnel, up to Director across the UK and internationally. ....Read more...
Type: Permanent Location: Birmingham, Leicester, Coventry, Northampton, England
Start: ASAP
Duration: Full-Time
Salary / Rate: £35000 - £37000 Per Annum Benefits
Posted: 2024-03-26 15:42:25
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PRODUCT SPECIALIST | SURREY | Competitive Salary
A global manufacturer of Enzymatic Indicator's are currently recruiting for a Product Specialist to join their growing team based in Surrey on a permanent basis (some hybrid working availability and global travel to be expected).
Reporting directly to the Technical Director, the core function of the role will be to develop, advance and lead customer understanding of the products and technology.
The key responsibilities are as follows:
Create and implement customer adoption projects and roll out programs
Contribute to new business initiatives and projects, reviewing and communicating the impact on Quality Management Systems
Grow a high level of EI product knowledge
Understand all aspects of gaseous (predominantly hydrogen peroxide) bio-decontamination processes, including validation strategies to lead customers in technology understanding
Have existing knowledge of hydrogen peroxide cycle development and validation
Have at least a basic microbiological understanding and strong capability relating to Biological Indicators
To be considered for the role candidates must have significant experience in an aseptic pharmaceutical production / manufacturing environment, along with microbiological and validations skills.
Strong knowledge of pharmaceutical quality management and experience of leading a team in a medical device / pharmaceutical quality environment is essential.
Prior experience of dealing with customers and suppliers would be preferred.
In order to apply for this role please forward your CV to melissa@blackfieldassociates.com or call Melissa on +44 (0) 2392 322 306 for further details.
STR Limited is acting as an Employment Agency in relation to this vacancy. ....Read more...
Type: Permanent Location: Surrey, England
Posted: 2024-03-26 11:29:04
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🌟 Job Opportunity: Locum Clinical Pharmacist Prescriber 🌟
We are seeking a dynamic and highly skilled Locum Clinical Pharmacist Prescriber to join our team immediately based in North Wales - Rhyl.
The position is for Tuesdays and Fridays with flexible timing.
📋 Position: Locum Pharmacist Prescriber
🚀 Start Date: As soon as possible
📅 Working Days: Tuesdays and Fridays
📆 Contract Duration: 8-10 weeks
⏰ Hours: Flexible timing
💰 Rate: £45 per hour (paying limited company)
📍 Location: Rhyl, Wales
Key Responsibilities:
🩺 Conducting clinical medication reviews.
💊 Providing expert advice on medications to healthcare professionals and patients.
📝 Prescribing medications within the scope of practice.
📈 Monitoring patient responses to drug therapy.
🤝 Collaborating with multidisciplinary teams to optimize patient care.
Requirements:
📜 Registration as a pharmacist with the General Pharmaceutical Council (GPhC).
💉 Independent prescribing qualification.
🏥 Proven experience working as a Clinical Pharmacist Prescriber in Primary care
💬 Excellent communication and interpersonal skills.
👥 Ability to work effectively in a multidisciplinary team.
🌟 Commitment to delivering high-quality patient care.
If you are a motivated and dedicated Clinical Pharmacist Prescriber looking for a rewarding locum opportunity, we want to hear from you!
To apply, please send your CV and cover letter to brett.smith@servicecare.org.uk with the subject line Locum Clinical Pharmacist Prescriber Application. ....Read more...
Type: Contract Location: Rhyl, Wales
Salary / Rate: £40 - £45 per hour
Posted: 2024-03-25 16:17:18
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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 are currently looking for a Calibration Engineer to join a leading Pharmaceutical company based in the Wiltshire area.
As the Calibration Engineer you will be responsible for Maintenance, calibration, repair, and continuous development of all process and utility equipment within the mechanical, electrical, instrumentation and control remit within the Engineering Department.
This is a Monday to Friday role and is site based.
KEY DUTIES AND RESPONSIBILITIES:
Your duties will be varied however the key duties and responsibilities are as follows:
1.
As the Calibration Engineer you will conduct requalification and calibration activities in adherence to the schedule and procedures.
2.
Maintain and use GMP documentation for all aspects of the job in accordance with working in a pharmaceutical environment.
3.
Aid with Installation, Operational, and Process Qualification processes for new and existing equipment.
4.
Organise and evaluate calibration data, looking for adverse trends and identifying failures.
ROLE REQUIREMENTS:
To be successful in your application to this exciting opportunity, we are looking to identify the following on your profile and past history:
1.
Qualification in an engineering discipline or closely related.
2.
Proven industry experience working to GMP guidelines.
3.
A working knowledge and practical experience within calibration of Pharmaceutical equipment.
Key Words: Engineer | Technician | Calibration | Pharmaceutical | GMP
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: Wiltshire,England
Start: 25/03/2024
Salary / Rate: £35000 - £40000 per annum
Posted: 2024-03-25 09:26:11
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We are currently looking for a Calibration Engineer to join a leading biopharmaceutical company based in the Hertfordshire area.
As the Calibration Engineer you will be responsible for Maintenance, calibration, repair, and continuous development of all process and utility equipment within the mechanical, electrical, instrumentation and control remit within the Engineering Department.
KEY DUTIES AND RESPONSIBILITIES:
Your duties will be varied however the key duties and responsibilities are as follows:
1.
Calibration of utility, process and laboratory instrumentation.
2.
Maintain and use GMP documentation for all aspects of the job in accordance with working in a pharmaceutical environment.
3.
Aid with Installation, Operational, and Process Qualification processes for new and existing equipment.
4.
Organise and evaluate calibration data, looking for adverse trends and identifying failures.
ROLE REQUIREMENTS:
To be successful in your application to this exciting opportunity, we are looking to identify the following on your profile and past history:
1.
Qualification in at least one engineering discipline
2.
Proven industry experience in the calibration of equipment, such as pressure, temperature, flow, pH, UV, conductivity, level and weight sensors.
3.
A working knowledge and practical experience within the highly regulated manufacturing industries:
Key Words: Engineer | Technician | Calibration | Pharmaceutical | GMP
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: Hertfordshire,England
Start: 25/03/2024
Salary / Rate: £35000 - £40000 per annum
Posted: 2024-03-25 09:14:03
