Open role
Quality Assurance Officer
- Aggregated by CV-Library
- Kent
- Permanent
- Full Time
Job Description
Talentmark are recruiting for a QA Officer on behalf of a growing manufacturer of Active Pharmaceutical Ingredients, to be based at their site in Kent on a permanent basis.
The Role:
This role offers exposure to the full Quality Assurance lifecycle and the opportunity to broaden your experience across multiple quality systems. You will be trusted to take ownership, contribute ideas and make a genuine impact within a growing business.
Key Responsibilities:
Maintaining and continually improving the Quality Management System (QMS).
Reviewing and approving batch manufacturing documentation prior to batch release, SOPs, controlled documents and quality records.
Managing Deviations, CAPAs, Change Controls, Complaints and OOS investigations and supporting product recalls and quality investigations where required
Supporting internal and supplier audits and assisting with customer and regulatory audits.
Supporting supplier qualification and Quality Agreements.
Maintaining training records and ensuring GMP compliance throughout the business.
Your Background:
Educated to degree level or above in Life Sciences or a related field.
Established Quality Assurance experience within a GMP pharmaceutical manufacturing environment.
Experience of QMS, CAPAs, Deviations, Change Controls and batch record review.
Ideally experience of internal or supplier audits, Validation and Supplier Quality.
Ability to write clear technical reports and quality documentation.
Excellent communication skills and confidence working across all departments
Benefits
Permanent full-time position
Monday-Friday working
31 days holiday (including Bank Holidays)
Company Pension
Company Bonus Scheme
Private Health Care
On-site parking
Access to on-site gym and Cafeteria
Apply:
It is essential that applicants hold entitlement to work in the UK. Please quote job reference (phone number removed) in all correspondence
The Role:
This role offers exposure to the full Quality Assurance lifecycle and the opportunity to broaden your experience across multiple quality systems. You will be trusted to take ownership, contribute ideas and make a genuine impact within a growing business.
Key Responsibilities:
Maintaining and continually improving the Quality Management System (QMS).
Reviewing and approving batch manufacturing documentation prior to batch release, SOPs, controlled documents and quality records.
Managing Deviations, CAPAs, Change Controls, Complaints and OOS investigations and supporting product recalls and quality investigations where required
Supporting internal and supplier audits and assisting with customer and regulatory audits.
Supporting supplier qualification and Quality Agreements.
Maintaining training records and ensuring GMP compliance throughout the business.
Your Background:
Educated to degree level or above in Life Sciences or a related field.
Established Quality Assurance experience within a GMP pharmaceutical manufacturing environment.
Experience of QMS, CAPAs, Deviations, Change Controls and batch record review.
Ideally experience of internal or supplier audits, Validation and Supplier Quality.
Ability to write clear technical reports and quality documentation.
Excellent communication skills and confidence working across all departments
Benefits
Permanent full-time position
Monday-Friday working
31 days holiday (including Bank Holidays)
Company Pension
Company Bonus Scheme
Private Health Care
On-site parking
Access to on-site gym and Cafeteria
Apply:
It is essential that applicants hold entitlement to work in the UK. Please quote job reference (phone number removed) in all correspondence