QC Compliance Specialist

Posted Yesterday
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Waterford, MI, USA
In-Office
48K-64K Annually
Entry level
Healthtech
The Role
Manages pharmaceutical QC compliance activities, including investigations, deviations, change controls, CAPAs, quality documentation, audits, and regulatory inspections. The role supports GMP compliance, develops QC compliance programs, coordinates issue resolution across functions, and leads continuous improvement initiatives. Candidates need pharmaceutical quality control experience, knowledge of GMP and FDA, EMA, and ICH requirements, audit and inspection experience, analytical problem-solving abilities, and strong communication skills.
Summary Generated by Built In

Job title: QC Compliance Specialist


  • Location: Waterford, Ireland
  • Job Type: Fixed Term Contract/12months
  • Working Arrangements: On-site, days role

About the job

At Sanofi, we’re committed to providing the next-gen healthcare that patients and customers need.

For more than 20 years, our Waterford team has continued to grow and diversify to serve patients around the world. Today, a team of almost 800 works together at a state-of-the-art biopharmaceutical and medical device campus. Recognized through multiple local and national awards, Sanofi Waterford offers flexible working and access to a world of opportunities to grow your career at one location. As well as attractive benefits, the team enjoy access to an onsite gym and medical Centre that underpin a strong commitment to health and wellbeing.

We are an innovative global healthcare company with one purpose: to chase the miracles of science to improve people’s lives. We’re also a company where you can flourish and grow your career, with countless opportunities to explore, make connections with people, and stretch the limits of what you thought was possible.


Key responsibilities:


The QC Compliance Specialist has a primary role in:


  • Representing QC for the processes led by QMS team at site level
  • Investigating in a timely manner and resolving any quality control events, issues, or discrepancies from his/her perimeter. Implementing remediation actions from findings and CAPAs
  • Managing the consolidated follow-up and progress tracking of events (eg deviation, lab investigations), change control and CAPAs, related to QC, coordinating with respective QC areas and other involved functions, to ensure they are managed and closed as committed
  • Contributing to develop, implement, and maintain an effective compliance program for QC
  • Ensuring issuance and approval of appropriate local quality control documentation, when required to support the QMS processes applicable to QC, in alignment with the site QMS
  • Investigating on a timely manner and resolving any quality control events, issues or discrepancies from his/her perimeter. Implementing remediation actions from findings and CAPAs
  • Providing support during regulatory inspections and audits
  • Leading initiatives for continuous improvement in QC, in coordination with QC excellence team
  • Ensure compliance to Good Manufacturing Practices (cGMP) at all times

About you

To excel in this role you will need to have:


  • Third Level qualification (degree in science or related discipline preferred)
  • Experience in quality control within the pharmaceutical industry, including knowledge of Good Manufacturing Practices (GMP) and regulatory requirements
  • Experience in managing internal audits and external regulatory inspections, including preparation, execution, and follow-up
  • In-depth understanding of pharmaceutical regulations, guidelines, and standards (e.g., FDA, EMA, ICH)
  • Ability to analyze complex compliance issues, identify root causes, and develop effective solutions
  • Proficiency in identifying issues and implementing effective solutions to resolve quality control problems
  • Strong verbal and written communication skills to effectively convey compliance requirements and updates to various stakeholders

Pursue Progress. Discover Extraordinary.

Join Sanofi and step into a new era of science - where your growth can be just as transformative as the work we do. We invest in you to reach further, think faster, and do what’s never-been-done-before. You’ll help push boundaries, challenge convention, and build smarter solutions that reach the communities we serve. Ready to chase the miracles of science and improve people’s lives? Let’s Pursue Progress and Discover Extraordinary – together.


At Sanofi, we provide equal opportunities to all regardless of race, color, ancestry, religion, sex, national origin, sexual orientation, age, citizenship, marital status, disability, gender identity, protected veteran status or other characteristics protected by law.


#LI-EUR

Pursue progress, discover extraordinary

Better is out there. Better medications, better outcomes, better science. But progress doesn’t happen without people – people from different backgrounds, in different locations, doing different roles, all united by one thing: a desire to make miracles happen. So, let’s be those people.

At Sanofi, we provide equal opportunities to all regardless of race, colour, ancestry, religion, sex, national origin, sexual orientation, age, citizenship, marital status, ability or gender identity.

Watch our ALL IN video and check out our Diversity Equity and Inclusion actions at sanofi.com!

The salary range for this position is :€48 000,00 - €64 000

Final compensation will be determined based on demonstrated experience, skills, location, and other relevant factors. Employees may be eligible to participate in Company employee benefit programs.

Skills Required

  • Third-level qualification in science or a related discipline
  • Experience in quality control within the pharmaceutical industry
  • Knowledge of Good Manufacturing Practices and regulatory requirements
  • Experience managing internal audits and external regulatory inspections, including preparation, execution, and follow-up
  • In-depth understanding of pharmaceutical regulations, guidelines, and standards, including FDA, EMA, and ICH
  • Ability to analyze complex compliance issues, identify root causes, and develop effective solutions
  • Ability to identify issues and implement effective solutions for quality control problems
  • Strong verbal and written communication skills

Sanofi Compensation & Benefits Highlights

The following summarizes recurring compensation and benefits themes identified from responses generated by popular LLMs to common candidate questions about Sanofi and has not been reviewed or approved by Sanofi.

  • Retirement Support — Retirement support stands out through a notably strong 401K matching structure (e.g., 150% match up to a 6% contribution), which materially boosts total rewards for long-tenured employees.
  • Parental & Family Support — Parental and family support is positioned as unusually robust, including a global gender-neutral paid parental leave standard (14 weeks) and added supports such as childcare assistance and adoption/surrogacy/infertility help.
  • Equity Value & Accessibility — Equity participation is made more accessible via an Employee Stock Purchase Plan that includes a meaningful purchase discount and matching/free-share mechanics, increasing perceived total compensation beyond base pay.

Sanofi Insights

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The Company
HQ: Paris
85,000 Employees
Year Founded: 1973

What We Do

We are Sanofi, an innovative global healthcare company. We chase the miracles of science to improve people’s lives. Our team, across some 100 countries, is dedicated to transforming the practice of medicine by working to turn the impossible into the possible. We provide potentially life-changing treatment options and life-saving vaccine protection to millions of people globally, while putting sustainability and social responsibility at the center of our ambitions. Interactions with this account must comply with the Terms: https://bit.ly/sanofi-terms

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