QA Officer

TN United Kingdom; Tredegar; On-site; GBP 30,000 - 50,000; Full time

Job summary

Join a forward-thinking company dedicated to life-changing therapies and global impact. As a QA Officer, you will play a crucial role in ensuring compliance with regulatory requirements and maintaining quality standards. This position offers an opportunity to work in a collaborative environment, where your contributions will help bridge the gap between innovative therapies and patients. With a commitment to employee well-being, the organization provides a competitive salary, generous leave, and development opportunities to support your career growth. Be part of a team that values progress and makes a meaningful difference.

Benefits

Employer Pension

Generous Annual Leave

Family-Friendly Benefits

Employee Referral Scheme

Health and Well-being Support

Cycle to Work Scheme

Development Opportunities

Qualifications

• Experience in a pharmaceutical environment under GMP is essential.
• Previous experience in a Quality department is desirable.

Responsibilities

• Produce compliance-related metrics for site Quality Management Reviews.
• Manage Customer Complaints and track corrective actions from audits.

Skills

GMP Skill Level 1

IT Proficiency

Quality Management

Self-motivation

Education

Pharmaceutical Experience

Quality Department Experience

Job description

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Life changing therapies. Global impact. Bridge to thousands of biopharma companies and their patients.

We are PCI.

Our investment is in people who make an impact, drive progress, and create a better tomorrow. Our strategy includes building teams across our global network to pioneer and shape the future of PCI.

The Role

The QA Officer QMS is responsible for assisting the QMS Team in ensuring QMS-related tasks are completed within the required timescales and in compliance with regulatory requirements.

Main responsibilities:

1. Produce compliance-related metrics for the site and assist in providing data for Quality Management Reviews.
2. Perform periodic updates of the Self-Inspection Schedule to ensure it is up to date.
3. Manage and administer Customer Complaints.
4. Track corrective and preventative actions from Internal and External audits.
5. Maintain and update the Approved Supplier List.
6. Coordinate external audits according to the required schedule.
7. Ensure Quality Agreements and TSE Statements are periodically updated within the required timeframes.
8. Assist in the generation of Nitrosamines Statements.
9. Author Product Quality Reviews.

Requirements

• Experience working within a pharmaceutical environment under GMP.
• GMP Skill Level 1 is essential.
• Proficiency in IT.
• Previous experience within a Quality department is desirable, ideally within a cGMP/pharma environment.
• Equivalent pharma industry experience.
• Self-motivated with the ability to achieve results through cooperation and influence.

At PCI, we believe that our employees are our most valuable asset. We are committed to providing a benefits package to support your well-being and enhance your overall quality of life. Our offerings include:

• Employer Pension: Secure your future with our employer pension scheme (above statutory pension).
• Competitive Salaries: Reflecting your dedication and contributions.
• Generous Annual Leave: 25 days plus bank holidays.
• Family-Friendly Benefits: Supporting your family life.
• Employee Referral Scheme: Refer someone perfect for our team and receive £500.
• Staff Engagement: Recognition schemes and long-service awards.
• Health and Well-being: Sick pay, 24/7 GP access, mental health support, and life assurance up to 4 times salary.
• Cycle to Work Scheme.
• Development Opportunities: Training programs, coaching, LinkedIn Learning, and further education.

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Join us and help build the bridge between life-changing therapies and patients.