3 Manufacturing Companies jobs in Caerphilly
Senior Pharmaceutical Quality Control Analyst
CF10 3AA Cardiff, Wales
£40000 Annually
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Posted today
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Job Description
Our client, a leading pharmaceutical company dedicated to advancing healthcare, is seeking a meticulous and experienced Senior Pharmaceutical Quality Control Analyst for their facility in Cardiff, Wales, UK . This role offers a hybrid work model, allowing for a balance of laboratory work and remote data analysis and reporting.
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:
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.
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.
This advertiser has chosen not to accept applicants from your region.
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Senior Pharmaceutical Quality Control Analyst
CF10 1AA Cardiff, Wales
£40000 Annually
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Posted 1 day ago
Job Viewed
Job Description
Our client, a rapidly growing pharmaceutical company, is seeking a highly skilled Senior Pharmaceutical Quality Control Analyst to join their dedicated team. This role, based in **Cardiff, Wales, UK**, offers a hybrid working arrangement, blending essential laboratory work with remote data analysis and reporting. You will be responsible for performing critical quality control testing on raw materials, in-process samples, and finished pharmaceutical products, ensuring compliance with stringent regulatory standards.
Key Responsibilities:
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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1
Senior Quality Control Manager (Automotive)
CF10 1AU Cardiff, Wales
£65000 Annually
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Posted 24 days ago
Job Viewed
Job Description
Our client is seeking a highly experienced Senior Quality Control Manager to lead their quality assurance efforts within the automotive manufacturing sector. This is a critical, fully remote role responsible for establishing, maintaining, and continuously improving robust quality control systems and processes across all stages of production. You will play a vital part in ensuring that all manufactured products meet the highest industry standards and customer expectations for reliability, safety, and performance.
The ideal candidate will possess a comprehensive understanding of automotive manufacturing processes, quality management systems (such as IATF 16949), and statistical quality control methodologies. Your responsibilities will include developing quality control plans, overseeing inspection and testing procedures, managing non-conformance reporting and corrective actions, and driving continuous improvement initiatives to reduce defects and enhance product quality. You will be adept at analysing quality data, identifying root causes of issues, and implementing effective solutions.
This fully remote position requires a leader who can effectively manage and mentor a geographically dispersed quality team. You will collaborate closely with engineering, production, supply chain, and customer support departments to foster a strong quality-focused culture throughout the organisation. Excellent communication, leadership, and problem-solving skills are essential. You will be responsible for reporting on quality metrics, driving compliance with regulatory requirements, and championing best practices in quality management. The ability to work autonomously, manage multiple priorities, and ensure consistent quality across all product lines is crucial.
Key Responsibilities:
The ideal candidate will possess a comprehensive understanding of automotive manufacturing processes, quality management systems (such as IATF 16949), and statistical quality control methodologies. Your responsibilities will include developing quality control plans, overseeing inspection and testing procedures, managing non-conformance reporting and corrective actions, and driving continuous improvement initiatives to reduce defects and enhance product quality. You will be adept at analysing quality data, identifying root causes of issues, and implementing effective solutions.
This fully remote position requires a leader who can effectively manage and mentor a geographically dispersed quality team. You will collaborate closely with engineering, production, supply chain, and customer support departments to foster a strong quality-focused culture throughout the organisation. Excellent communication, leadership, and problem-solving skills are essential. You will be responsible for reporting on quality metrics, driving compliance with regulatory requirements, and championing best practices in quality management. The ability to work autonomously, manage multiple priorities, and ensure consistent quality across all product lines is crucial.
Key Responsibilities:
- Develop, implement, and manage the company's quality control strategy and policies.
- Oversee all aspects of product quality, from incoming materials to final product inspection.
- Ensure compliance with IATF 16949 and other relevant automotive quality standards.
- Lead and mentor the remote quality control team, setting performance objectives and providing guidance.
- Establish and monitor key quality performance indicators (KPIs) and report on quality metrics.
- Implement statistical process control (SPC) techniques to monitor and improve manufacturing processes.
- Manage the non-conformance process, including root cause analysis and the implementation of corrective and preventive actions (CAPA).
- Collaborate with engineering and production teams to resolve quality issues and improve product design.
- Drive continuous improvement initiatives to enhance product quality and reduce manufacturing costs.
- Conduct internal audits and support external audits by customers and regulatory bodies.
- Bachelor's degree in Engineering (Mechanical, Manufacturing, Electrical) or a related field.
- Minimum of 8 years of experience in quality control or quality assurance, with at least 3 years in a management role within the automotive manufacturing industry.
- In-depth knowledge of IATF 16949 standards and quality management systems.
- Proficiency in statistical quality control tools and methodologies (SPC, Six Sigma, Lean Manufacturing).
- Experience with root cause analysis techniques (e.g., 8D, FMEA).
- Strong leadership, team management, and communication skills.
- Proven ability to drive continuous improvement and achieve quality objectives.
- Excellent analytical and problem-solving capabilities.
- Ability to work independently and manage a remote team effectively.
This advertiser has chosen not to accept applicants from your region.
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