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Quality Control (QC) Analyst
Posted 3 days ago
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Job Description
Blue Arrow is recruiting a Quality Control (QC) Analyst to join our clients team based in the Llantrisant area.
Salary : 27,000p.a
Hours : 4 days on, 4 days off, 10-hour shifts from 07:00 to 18:00
Contract : 6 month fixed term contract
Role Overview
As a QC Analyst, you will be responsible for conducting a variety of laboratory tests and analyses to ensure our products meet regulatory standards and client specifications. You will play a key role in monitoring production processes, identifying deviations, and implementing corrective actions to maintain the integrity and safety of our products.
Main Responsibilities
Perform routine and non-routine analyses of raw materials, in-process samples, and finished products using established analytical techniques (e.g., FPLC, UV-Vis, FTIR, titration, wet chemistry).
Interpret and report analytical results accurately, maintaining detailed and organised records in compliance with Good Laboratory Practices (GLP) and company SOPs.
Calibrate, operate, and maintain laboratory equipment, ensuring all instruments are functioning optimally and maintaining calibration logs as required.
Participate in method development, method validation, and continuous improvement initiatives to optimise laboratory performance.
Conduct investigations into non-conforming results and work collaboratively to determine root causes and implement effective corrective actions.
Assist in the preparation and review of technical documents such as SOPs, test methods, specifications, and validation protocols.
Support internal and external audits by providing necessary documentation, data, and explanations regarding laboratory practices and results.
Ensure all laboratory activities are conducted in accordance with health, safety, and environmental regulations.
Collaborate with cross-functional teams, including production, quality assurance, and research and development, to resolve quality issues and drive continuous improvement.
Stay current with advances in analytical techniques, regulatory requirements, and industry best practices.
Requirements
Bachelor's degree in chemistry, Biochemistry, Pharmaceutical Science, Microbiology, Food Science, or a related scientific discipline.
Familiarity with analytical instrumentation (e.g., HPLC, GC, UV-Vis, FTIR) and associated software.
Strong understanding of GLP, GMP, or ISO standards as applicable to the industry.
Excellent attention to detail, time management, and organisational skills.
Strong communication abilities, both written and verbal, and ability to convey technical information clearly.
Problem-solving skills and an investigative mindset.
Ability to work independently as well as collaboratively in a fast-paced, team-oriented environment.
Proficient in using standard office and laboratory software (e.g., Microsoft Office, LIMS).
Desirable Skills
Experience with method development and validation.
Knowledge of statistical analysis and data interpretation.
Familiarity with regulatory submissions and documentation (e.g., MHRA, FDA, EMA).
Previous experience in root cause analysis and CAPA (Corrective and Preventive Action) processes.
Additional language skills are an advantage.
If you feel you would be suitable for the above role, please submit your CV for immediate response.
Blue Arrow is proud to be a Disability Confident Employer and is committed to helping find great work opportunities for great people.
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Senior Pharmaceutical Quality Control Analyst
Posted today
Job Viewed
Job Description
The Senior Pharmaceutical Quality Control Analyst will be responsible for performing a wide range of analytical tests on raw materials, in-process samples, and finished pharmaceutical products to ensure they meet strict quality and regulatory standards. This includes conducting assays, identifying impurities, and verifying product identity and potency using various analytical techniques and instruments.
Key responsibilities include operating and maintaining sophisticated laboratory equipment such as HPLC, GC, UV-Vis spectrophotometers, and dissolution apparatus. You will meticulously document all test procedures, results, and observations in accordance with Good Manufacturing Practices (GMP) and regulatory guidelines. The role also involves method development and validation, troubleshooting analytical issues, and contributing to the continuous improvement of quality control processes. You will play a vital role in ensuring the safety and efficacy of pharmaceutical products.
Qualifications and Experience:
- Bachelor's or Master's degree in Pharmacy, Chemistry, Pharmaceutical Science, or a related life science discipline.
- A minimum of 5 years of hands-on experience in pharmaceutical quality control or analytical testing.
- Proficiency in various analytical techniques, including HPLC, GC, Karl Fischer titration, and dissolution testing.
- Strong understanding of GMP, ICH guidelines, and other relevant regulatory requirements.
- Experience with laboratory information management systems (LIMS) is desirable.
- Excellent attention to detail and accuracy in experimental work and data recording.
- Strong problem-solving skills and the ability to troubleshoot analytical instrumentation and methods.
- Effective communication and interpersonal skills, with the ability to collaborate with cross-functional teams.
- Experience in method development and validation is a significant advantage.
- Ability to work independently and manage multiple tasks effectively.
This is a critical role within the pharmaceutical industry, ensuring the highest standards of quality and compliance for life-saving medications. Join a team committed to excellence and innovation in pharmaceutical development.
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Senior Pharmaceutical Quality Control Analyst
Posted today
Job Viewed
Job Description
Key Responsibilities:
- Perform a range of analytical tests on pharmaceutical raw materials, intermediates, and finished products using techniques such as HPLC, GC, UV-Vis, IR, and titration.
- Develop, validate, and transfer analytical methods according to regulatory guidelines (e.g., ICH).
- Interpret test results, analyse data, and prepare accurate and comprehensive Certificates of Analysis (CoAs).
- Investigate out-of-specification (OOS) results and deviations, identifying root causes and implementing corrective and preventive actions (CAPAs).
- Maintain laboratory equipment, perform calibration and qualification, and ensure compliance with GLP/GMP standards.
- Contribute to the continuous improvement of quality control processes and procedures.
- Collaborate with R&D, production, and regulatory affairs departments to support product development and troubleshooting.
- Ensure all laboratory activities are conducted in compliance with internal SOPs and relevant regulatory requirements (e.g., MHRA, FDA).
- Assist in the training and mentoring of junior QC analysts.
- Prepare and review method validation protocols and reports.
- Manage laboratory documentation and records ensuring data integrity.
- Bachelor's or Master's degree in Chemistry, Pharmaceutical Science, or a related scientific discipline.
- Minimum of 5 years of experience in pharmaceutical quality control or a related analytical laboratory role.
- Hands-on experience with a variety of analytical techniques, particularly HPLC and GC, is essential.
- Strong understanding of Good Laboratory Practice (GLP) and Good Manufacturing Practice (GMP) regulations.
- Experience with method development and validation is highly desirable.
- Excellent analytical and problem-solving skills, with a keen eye for detail.
- Proficiency in data analysis and interpretation, with strong report-writing skills.
- Ability to work effectively both independently and as part of a team.
- Familiarity with laboratory information management systems (LIMS).
- Effective communication skills for cross-departmental collaboration.
- Willingness to work in a hybrid model, with flexibility for on-site laboratory work in **Cardiff, Wales, UK**.
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