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QA Specialist - QMS

PCI Pharma Services

Tredegar

On-site

GBP 60,000 - 80,000

Full time

Today
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Job summary

A leading pharmaceutical company located in Tredegar is searching for a QA Specialist to support its Quality Management System. This on-site role demands strong regulatory knowledge, attention to detail, and the ability to work independently while providing guidance across departments. The successful candidate will coordinate vendor audits, manage customer complaints, and oversee quality documentation. Competitive salaries, generous leave, and health benefits are part of the offered package.

Benefits

Employer Pension
Competitive Salaries
Generous Annual Leave
Family Friendly Benefits
Employee Referral Scheme
Health and Well-being support
On-Site Subsidised Canteen
Cycle to Work Scheme
Development Opportunities

Qualifications

  • Experience in a similar pharmaceutical role required.
  • Strong interpersonal and communication skills, commitment to continuous improvement.
  • Completion-driven mindset with attention to detail.

Responsibilities

  • Coordinate and complete external vendor audits.
  • Manage customer complaint investigations and corrective actions.
  • Maintain and update the Approved Supplier List.

Skills

Interpersonal skills
Communication skills
Attention to detail
Vendor management
Risk management
Job description

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.

Role Summary

The QA Specialist QMS is responsible for supporting and maintaining the Quality Management System at PCI Tredegar.

This fully on-site role requires strong technical and regulatory knowledge, attention to detail, and a commitment to quality and continuous improvement. The job holder will work largely independently under the supervision of the QMS Manager, providing guidance, training, and support across the site while upholding PCI’s values and regulatory standards.

Main Responsibilities
  • The QA Specialist coordinates and completes external vendor audits according to an agreed programme, ensuring compliance with PCI procedures, risk assessments, and cost‑effectiveness. They manage, administer, and approve customer complaint investigations, ensuring thorough assessment and documentation of issues.
  • Tracking corrective and preventive actions from internal and external audits is a key responsibility, including closing actions where possible or supporting other departments to achieve closure. The role requires regular use of the PCI Tredegar quality system software, Master Control, to manage corrective and preventive actions, client audits, and supplier assessments.
  • The QA Specialist maintains and updates the Approved Supplier List and reports relevant Key Performance Indicators. Compliance with company policies, procedures, and internal/external Health, Safety and Environmental standards is mandatory.
  • The role involves undertaking projects within the job holder’s capabilities, proactively identifying opportunities for continuous improvement, and reviewing and improving departmental processes to eliminate waste. Conducting GxP training and contributing to training materials is also part of the role, alongside ensuring timely review and approval of quality documentation.
  • The job holder collates Quality Management Review (QMR) information for senior management, applies Quality Risk Management principles, investigates deviations, errors, failures, and adverse events, and uses professional judgment to support product quality decisions in collaboration with site Qualified Persons.
  • Additional responsibilities include reviewing and approving extensions and justifications, managing the Product Quality Review (PQR) schedule, hosting internal meetings, facilitating PPS meetings, completing customer questionnaires, and updating policies and procedures. The role also requires identifying personal development needs to support future growth.
Requirements
  • Experience in a similar pharmaceutical role is required, with credentials covering both investigational and marketed products.
  • Strong interpersonal and communication skills, a commitment to continuous improvement, effective planning, and the ability to manage multiple tasks simultaneously are essential.
  • A completion‑driven mindset with attention to detail, experience in vendor management.
  • Desirable experience in risk management and PQR completion are important for success in this role.
Benefits

At PCI, we believe that our employees are our most valuable asset. That's why we are committed to providing a benefits package designed to support your well‑being and enhance your overall quality of life. Here's what we offer:

  • Employer Pension: Secure your future with our employer pension scheme (above statutory pension).
  • Competitive Salaries: We offer competitive salaries that reflect your dedication and contributions.
  • Generous Annual Leave: Enjoy 25 days of annual leave, plus bank holidays.
  • Family Friendly Benefits: Enjoy a range of benefits designed to support your family life.
  • Employee Referral Scheme: Know someone perfect for our team? Refer them and receive £500 as our way of saying thank you!
  • Staff Engagement: We value your dedication with recognition schemes and long‑service awards.
  • Health and Well‑being: Your health matters. Count on our support with generous sick pay, access to a 24/7 GP through our employee assistance program, mental health support, and life assurance up to 4 times your annual salary.
  • On‑Site Subsidised Canteen.
  • Cycle to Work Scheme.
  • Development Opportunities: Invest in your future with our training programs, coaching opportunities, LinkedIn Learning, and further education options.

Join us and be part of building the bridge between life‑changing therapies and patients. Let’s talk future.

Equal Employment Opportunity (EEO) Statement

PCI Pharma Services is an Equal Opportunity/Affirmative Action Employer. We do not unlawfully discriminate on the basis of race, color, religion, age, sex, creed, national origin, ancestry, citizenship status, marital or domestic or civil union status, familial status, affectional or sexual orientation, gender identity or expression, genetics, disability, military eligibility or veteran status, or any other protected status.

At PCI, Equity and Inclusion are at the core of our company’s purpose: Together, delivering life‑changing therapies. We are committed to cultivating an inclusive workplace by holding ourselves accountable to the highest standards of understanding, fairness, respect, and equal opportunity – at every level. We envision a PCI community where everyone can belong and grow, and we strive to bring this vision to reality by continuously and intentionally assessing our people practices, policies and programs, marketing approach, and workplace culture.

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