Skip to the page

Quality Assurance Pharmacist

ExcelyaWorkableBoulogne-Billancourt, Île-de-France, France
Posted 13 OctFound 22 OctSeen 2 hours ago

Fit

The keywords the posting names, against what your resume says.

Add your resume to see which of its keywords you already have, and get a resume tailored to this posting. 10 a month, free.

The Posting

At Excelya, we combine passion, scientific excellence, and collaboration to support our clients throughout the entire drug development lifecycle. We encourage our employees to be bold, take initiative, and unlock their full potential in an international, fast-growing environment.

We are currently looking for a Quality Assurance Pharmacist to strengthen our Quality team and support pharmaceutical quality systems, product quality activities, and regulatory compliance initiatives.

Key responsibilities: Quality Management System (QMS)

  • Manage and maintain quality documentation including SOPs, procedures, and quality records.
  • Coordinate document lifecycle activities, including creation, review, approval, archiving, and periodic reviews.
  • Support and deliver GxP and quality-related training programs.
  • Participate in internal audits, supplier audits, and health authority inspections.
  • Manage quality events including deviations, CAPAs, change controls, and continuous improvement initiatives.
  • Ensure compliance with applicable pharmaceutical regulations and quality standards.

Product Quality Activities

  • Manage product quality complaints and associated investigations.
  • Support quality defect reporting and interactions with health authorities when required.
  • Conduct risk assessments and quality impact evaluations.
  • Participate in product recall and shortage management activities.
  • Review Product Quality Reviews (PQRs) and monitor quality trends.
  • Review and approve batch release documentation and distribution-related quality activities.

Quality Oversight & Continuous Improvement

  • Monitor quality KPIs and performance indicators.
  • Contribute to Management Reviews and Annual Quality Reviews.
  • Support cross-functional initiatives such as product launches, technology transfers, and portfolio optimization projects.
  • Drive quality culture and promote continuous improvement across the organization.
  • Collaborate closely with Manufacturing, Supply Chain, Regulatory Affairs, Pharmacovigilance, and Quality stakeholders.

Requirements

Education

  • Doctor of Pharmacy (PharmD) mandatory.
  • Strong experience in Quality Assurance within the pharmaceutical industry.
  • Experience in pharmaceutical manufacturing or production environments is highly desirable.
  • Registration as a Responsible Pharmacist (PRI) is considered an asset.

Technical Skills

  • Strong knowledge of: GMP (Good Manufacturing Practices) GDP (Good Distribution Practices), GVP and Pharmacovigilance requirements
  • Proven experience managing: Deviations, CAPAs, Change Controls, Root Cause Analysis (RCA), Risk Management activities
  • Experience with Quality Management Systems and tools such as: TrackWise, EDMS, SAP, Other electronic Quality Systems

Language

  • Fluent English, both written and spoken.

Benefits

Why join us?

At Excelya, we combine a passion for science with the enthusiasm of teamwork to redefine excellence in healthcare.

Here's what makes us unique:

We are a young and ambitious healthcare company, bringing together 900 Excelyates, driven by the goal of becoming the leading mid-sized CRO in Europe, while offering the best employee experience.

Our "one-stop provider" service model—combining full-service, functional service provider, and consulting—allows you to grow through diverse and stimulating projects. By collaborating with leading experts, you will contribute to the development of scientific, operational, and human knowledge, all in service of improving the patient journey.

Excelling with kindness means evolving in an environment that values ​​your natural talents, encourages boldness, pushes boundaries, and cultivates your potential, so that you can fully contribute to our shared mission.

Facts

Source
Workable
External id
D561B3C777
Location
Boulogne-Billancourt, France
Remote
Not stated
Employment
Full time
Posted
13 Oct 2026
First seen
22 Oct 2026, 09:27
Last seen
1 Nov 2026, 15:16
Status
Not yet added
Posting id
ef1fe92a-a692-5ef5-a5e5-4b76fe57d15e