Quality Control Specialist
An opportunity has arisen for a Quality Control Specialist to join the growing team of scientists based in the southwest area. The successful individual has a working knowledge of Quality, GMP and GLP practices.
The Quality Control Specialist will play a vital role in ensuring adherence to quality standards, GMP (Good Manufacturing Practice), and GLP (Good Laboratory Practice) guidelines. The successful candidate will be responsible for coordinating product releases, managing complaints, maintaining QA-related records, and participating in corrective and preventive action activities.
Key Responsibilities:
- Coordinate product releases in compliance with cGMPs and company SOPs.
- Log and review complaints, ensuring timely resolution.
- Maintain QA-related manufacturing records and CAPA (Corrective and Preventive Action) records.
- Manage calibration and qualification records.
- Participate in corrective and preventive action activities.
- Review standards and procedures of operation and conduct audits as necessary.
- Implement verification and validation strategies in alignment with relevant regulatory guidelines.
- Work with minimal supervision, demonstrating initiative and accountability.
Education and Experience:
- BSc or MSc degree in Biological Sciences or a related field.
- 5-10 years of relevant working experience, preferably in the biomedical or pharmaceutical industry.
- A certificate in Regulatory Affairs or Quality Control is desirable.
Skills and Qualifications:
- Attention to detail with the ability to work independently and in a team environment.
- Strong multitasking abilities with a proactive "can-do" attitude.
- Excellent problem-solving and communication skills.
- Proficiency in Microsoft Office tools (Excel, Word, Project, PowerPoint).
- Strong interpersonal skills with the ability to communicate effectively both orally and in writing.
Skills: QC, Management, Regulatory affairs, QA. GMP/GLP, Life Science, Pharmaceutical, Biomedical
To apply for this position, candidates must be living in the UK and eligible to work.
Required skills
- Compliance
- Management
- Manufacturing
- Regulatory Affairs
- Biomedical Sciences
- Pharmaceutical Industry
- QA/QC
- GMP/GLP
Reference: 52465637
Please note Reed.co.uk does not communicate with candidates via Whatsapp, and we will never ask you to provide your bank, passport or driving licence details during the application process. To stay safe in your job search and flexible work, we recommend visiting JobsAware, a non-profit, joint industry and law enforcement organisation working to combat labour market abuse. Visit the JobsAware website for information and free expert advice for safer work.
Report this jobNot quite what you are looking for? Try these similar searches
Replace a job alert
Replace a job alert
Get Job Alerts straight to your inbox
"Office Assistant jobs in London"
Your Job Alert has been created and your search saved.
'Saved search name'