Perrigo Posted October 23, 2026

Quality Assurance Associate (Ghent, BE, 9050)

Ghent, Belgium Type not listed
Quality Associate
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Perrigo is the source of truth for this posting and owns the application process. We surface normalized context and market comparison you won't find on the original listing.

About this opportunity

At Perrigo, we are driven by our mission to Makes Lives Better Through Trusted Health and Wellness Solutions, Accessible to All . We are proud to be a Top 10 player in the European Consumer Self-Care market and the largest U.S. store brand provider of over the counter and infant formula. Dedicated to providing The Best Self-Care for Everyone , we are the people behind the brands you trust. We are Opill®, Compeed®, Solpadeine®, NiQuitin®, and many more. We Are Perrigo. We are committed to enhancing the wellbeing of our colleagues and consumers alike. We pride ourselves on fostering an inclusive, collaborative culture where each person can experience a sense of belonging.

Join us on our One Perrigo journey as we evolve to win in self-care.

Description Overview

Perrigo is a leading global provider of over-the-counter (OTC) health products and wellness solutions that enhance individual overall well-being. Originating from the former Omega Pharma, the European branch is today present in 30 countries with a strong local anchorage.

You know us from brands like Compeed, Ella One, Norlevo, Physiomer, NiQuitin, XLS Medical, Zaffranax, Arterin, Dermalex, Biover, Galenco, Davitamon, Ymea, Lactacyd. Perrigo is an organization with a dynamic, transparent and fast-paced atmosphere, characterized by an entrepreneurial and cooperative culture.

The Quality Assurance Associate is in charge of Perrigo Medical Devices products for:

• CMO Management: responsible for all QA activities associated with the management of the CMOs under his/her responsibility.

• Product Quality Management: responsible for all QA activities related to the products under his/her responsibility associated with the development of new products, manufacturing line transfers, stability studies and validation activities.

• Technical File redaction: responsible for the preparation of the Manufacturing, Quality and stability sections of the technical files related to the products under his/her responsibility

• Support the maintenance of the Quality Management System: ensure that the SOP and templates used in daily activities are up to date and compliant with the relevant standards.

• Coordinate operational activities: collaborating with all the relevant stakeholders, the Quality Assurance Specialist ensures that Perrigo products are at any time compliant with the relevant regulation and standards. He/she provides QA expertise to all departments.

Scope of the Role

1.CMO Management

a.Prepare, maintain and control Quality agreements.

b.Build and maintain relationships with the relevant stakeholders at the CMO site.

c.Review, challenge and approve the protocols/reports provided by the CMO.

d.Facilitate the communication between the CMO and Perrigo

2.Product Quality Management

a.Preparation, review and approval of validation activities

b.Follow-up on ongoing stability studies

c.Active participation in the dedicated product category meetings

d.Participation in transfer activities, if needed

e.Reporting to line manager of critical activities and projects status

3.Quality Management System

a.Responsible for updating relevant SOP under his/her scope

b.Maintenance of database and documentation

c.Ensure a close follow-up and a timely execution of all Quality processes related to his/her products.

d.Contribute to the identification of GAP and point of improvement in the QMS

e.Support during Notified Boby audits, if necessary

4.Coordinate Operational activities

a.Open and manage non-conformities, deviations, change controls, CAPA and other relevant QA processes

b.Ability to perform audits of manufacturers under ISO13485 and MDR scopes

c.Support business needs

Experience Required

Scientific background, with 8 to 10 years of experience in the life-science industry and Medical Devices management

•Ideally, > 5 years in quality assurance.

Skills :

Mandatory :

•Good knowledge of ISO13485 and MDR

•Medical Devices experience (manufacturing and technical files)

•Certified ISO13485 auditor

•Knowledge about Cosmetics, Biocides or Food supplements is a plus

•Good IT knowledge and skills

Profile:

-Self-starter, capable of working autonomously at corporate level.

-Clear communicator, practical and solution orientated.

-Enthusiastic and get the job done.

-Strong project management skills & team worker in a multicultural environment.

-Persistent drive for results in a fast-paced environment, utilizing sound project focus, organizational and problem solving skills.

-You speak and write fluently English. Other languages are an asset.

-An innovative frame of mind – open to applying creative techniques to find a solution

Benefits

We believe our people are our greatest asset. Alongside competitive compensation, we offer benefits tailored to supporting you and your family, as well as career development opportunities to ensure you feel valued and supported, both professionally and personally.

Find out more about  Total Rewards  at Perrigo.

Hybrid Working Approach

We love our offices and the setting they provide for in-person collaboration and celebration. But we also appreciate the opportunity to work remotely can energise you too, so we promote flexibility with the ability to work two days a week from home in many roles.

We are proud to be included in the Forbes list of "America's Best Employers by State 2024". Find out more  here

Applicants please note: To apply to this position please click the APPLY button at the bottom of the application.  (The SAVE button will only save your profile information but not submit an application for this open position.) All application materials, including resumes and CVs, must be submitted in English. Thank you.

We are an equal opportunity employer. All qualified applicants will receive consideration for employment without regard to race, color, religion, sex, sexual orientation, gender identity, national origin, disability, status as a protected veteran, or other characteristics protected by law.  #weareperrigo

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Job details

Seniority
Associate
Function
Quality
Therapeutic area
Not listed
Location
Ghent, Belgium
Employment type
Not listed

How this role compares

Computed from every other active Quality role in our database, not just this employer's listings.

We currently track 370 comparable Associate Quality roles across 78 biopharma companies.

370Comparable roles tracked
339Currently active
78Companies hiring similar roles
31Countries represented

Salary context

52 of 370 peers report a salary range (USD, annualized)

Peers share this role's job function and a matching or adjacent seniority level -- not necessarily the same therapeutic area or country.

This roleSubject Not listed on this posting
Lowest disclosed · Associate Quality Control Analyst (Virology) · Regeneron Pharmaceuticals, Inc (USA) $22/hr – $34/hr (≈ $45,302–$70,699/yr)
Highest disclosed · Senior Manager, Quality Management Systems · Johnson & Johnson $142,000/yr – $244,950/yr
Peer group range $58,001 – $193,475 (median $159,000)

Where these roles are based

Top locations among the 370 comparable roles

United States136
Germany42
France38
China24
Ireland20
India18

+ 25 more countries

Seniority mix

370 of 370 peers have a known seniority level

Manager202
Intern/Fellow/Postdoc97
Associate71

Therapeutic area mix

0 of 370 peers have a known therapeutic area; the rest are genuinely unlabeled, not hidden

No peers with a known therapeutic area yet.

Similar opportunities

The closest matches from our peer group, ranked by how similar they are, not how well you'd qualify for them -- treat this as market context, not a guaranteed shortlist; a weak match is labeled as one below.

60%similar
Novartis Puurs, Belgium Associate
Same function Same seniority Same country
50%similar
GlaxoSmithKline Biologicals S.A. Belgium-Wavre, Belgium Intern/Fellow/Postdoc
Same function Adjacent seniority Same country
50%similar
GlaxoSmithKline Biologicals S.A. Belgium-Wavre, Belgium Intern/Fellow/Postdoc
Same function Adjacent seniority Same country
50%similar
UCB Braine L'alleud, Walloon Brabant, Belgium Manager
Same function Adjacent seniority Same country
50%similar
UCB Braine L'alleud, Walloon Brabant, Belgium Manager
Same function Adjacent seniority Same country
50%similar
GlaxoSmithKline Biologicals S.A. Belgium-Wavre, Belgium Intern/Fellow/Postdoc
Same function Adjacent seniority Same country

Notify me about similar jobs

Get an email when we spot other openings like this one – same job function, comparable seniority, roles you'd actually want to see.

Or follow a whole field: get every new Quality job in Belgium, and choose locations and companies.

How we calculate "similar"

No black box, no LLM guesswork: a deterministic score built from four normalized attributes. Here's this role's own peer group at different match levels, so you can see the mechanism, not just the result.

Every comparison starts from the same 100-point budget: 25 for working in the same function, 40 for the same therapeutic area, 20 for the same or adjacent seniority, 15 for the same country. A dimension we can't confirm on both sides contributes nothing, never a guess, never a free pass.

60%
Associate Quality Assurance Compliance Expert - QMS
Novartis · Puurs, Belgium · Associate
Function Therapeutic area Seniority Country
50%
Bio DS Operations Quality Manager Weekend
UCB · Braine L'alleud, Walloon Brabant, Belgium · Manager
Function Therapeutic area Adjacent seniority Country
50%
Stage : Project Management, QC Business Operations Performance & Strategy, Belgique - 2026
GlaxoSmithKline Biologicals S.A. · Belgium-Wavre, Belgium · Intern/Fellow/Postdoc
Function Therapeutic area Adjacent seniority Country
45%
Associate, Quality Assurance, Manufacturing Operations, Lilly Medicine Foundry
Lilly · Lebanon, Indiana, United States of America · Associate
Function Therapeutic area Seniority Country
Unmatched or unknown dimensions score exactly the same: 0 points, never a partial guess. A role we know almost nothing about beyond its function bottoms out at 25%; it never inflates to 100% just because there's little to compare against. Seniority uses a defined ladder (Associate → Manager → Associate Director → Senior → Principal → Director → Senior Director → Executive/VP) so "Director" and "Senior Director" count as adjacent, but "Director" and "Executive/VP" do not.