Teva Pharmaceuticals Posted August 28, 2026

Quality Compliance Associate

Amsterdam, Netherlands Type not listed
Quality Associate
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Teva Pharmaceuticals 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

We Are Teva

We’re Teva, a leading innovative biopharmaceutical company, enabled by a world-class generics business. Whether it’s innovating in the fields of neuroscience and immunology or delivering high-quality medicine worldwide, we’re dedicated to addressing patients’ needs now and in the future. Here, you will be part of a high-performing, inclusive culture that values fresh thinking and collaboration. You'll have the room to grow, the flexibility to balance life with work, and the opportunity to better health worldwide, together.

Our Team, Your Impact

As the Quality Compliance Associate you will support the site's Quality Systems & Compliance team in maintaining quality at the department in accordance with Site SOP’s, Teva Global Standards, regulatory guidelines and cGXP compliance requirements.

You will manage high standards of quality at the department through continuously improving the effectiveness of the department quality processes and systems.

Key Responsibilities

Prepare and support department policies and objectives in line with Teva and Site policies.

Coordinate and execute the implementation of Teva standards and procedures at the site.

Ensure the implementation of and compliance with national and international quality standards (cGXP) as well as Teva Global standards.

Organize the evaluation of vendors and approve and maintain their Qualification status, including Quality Technical Agreements.

Assure robust inspection preparation systems that include the organization of front and back office as well as the training of SME’s.

Support inspection preparation as well as support of front and back office during inspections.

Use analyses to identify root causes and determine CAPAs Recognizes when changes in product, process or regulations will require changes in tasks and plans accordingly.

Fulfillment of the Data Integrity Site Champion

Initiate, coordinate, support, and close out Data Integrity projects

Ensure timely implementation of Data Integrity projects

Assure Data Integrity awareness at all levels of the organization.

Ensure permanent inspection readiness on the site.

Share best practices, challenges and lessons learned within the site across the Teva Quality organization in order to improve the performance of quality globally.

Monitor and adjust day-to-day performance and operations.

Your Skills and Experience

University degree in Pharmacy, Chemistry, or a related scientific discipline, or HBO+ level education with several years of experience in a Quality role within the pharmaceutical industry

Proven experience with pharmaceutical processes, quality systems, and cGXP requirements

Familiarity with process automation in a regulated environment.Good understanding of cGxP, data integrity, and relevant regulatory requirements

Ability to translate SOPs and quality requirements into practical day-to-day operations

Knowledge of applicable regulatory and pharmacopeial guidelines

Experience supporting inspections and audits and working with cross-functional teams

A proactive, positive, and solution-oriented mindset

Fluent in English (essential); Dutch language skills are considered a strong advantage.

How We’ll Take Care of You

At Teva, better health starts from within, and that includes you. From day one, you’ll be supported with benefits designed to help you thrive in and out of work. This includes generous annual leave, reward plans, flexible working schedules (dependent on role), access to tailored health support, and meaningful ways to give back to the community.  When it comes to your career, you’ll be encouraged to explore, evolve, and shape your path. Twist, our one-stop shop for career development platform, gives you access to a wide range of possibilities, from learning programs and short-term projects to opportunities for internal growth. Here, you’ll be part of a culture that empowers you to reach your goals and prioritize your wellbeing every step of the way.

Already Working @Teva?

Make sure to apply through our internal career site on Twist, your one-stop shop for career development

The deadline for internal applications will close on Friday 18th September 2026

Teva’s Equal Employment Opportunity Commitment

Teva Pharmaceuticals is committed to equal opportunity in employment. It is Teva's global policy that equal employment opportunity be provided without regard to age, race, creed, color, religion, sex, disability, pregnancy, medical condition, sexual orientation, gender identity or expression, ancestry, veteran status, national or ethnic origin or any other legally recognized status entitled to protection under applicable laws. We are committed to a diverse and inclusive workplace for all. If you are contacted for a job opportunity, please advise us of any accommodations needed to support you throughout the recruitment and selection process. All accommodation information provided will be treated as confidential and used only for the purpose of providing an accessible candidate experience.

Job details

Seniority
Associate
Function
Quality
Therapeutic area
Not listed
Location
Amsterdam, Netherlands
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 249 comparable Associate Quality roles across 70 biopharma companies.

249Comparable roles tracked
234Currently active
70Companies hiring similar roles
30Countries represented

Salary context

52 of 249 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
Highest disclosed · Senior Manager, Quality Assurance (GMP Operations) · Gilead Sciences, Inc. $157,590/yr – $203,940/yr
Peer group range $75,510 – $180,765 (median $157,695)

Where these roles are based

Top locations among the 249 comparable roles

United States88
Germany29
China20
Ireland13
Belgium12
Netherlands10

+ 24 more countries

Seniority mix

249 of 249 peers have a known seniority level

Manager161
Intern/Fellow/Postdoc51
Associate37

Therapeutic area mix

0 of 249 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
BMS Netherlands Operations B.V. Leiden – NL, Netherlands Associate
Same function Same seniority Same country
60%similar
Johnson & Johnson Leiden, Netherlands Associate
Same function Same seniority Same country
60%similar
BMS Netherlands Operations B.V. Leiden – NL, Netherlands Associate
Same function Same seniority Same country
60%similar
NV Organon (Netherlands) Nld, Netherlands Associate
Same function Same seniority Same country
50%similar
NV Organon (Netherlands) Nld, Netherlands Manager
Same function Adjacent seniority Same country
50%similar
Perrigo Rotterdam, Netherlands Manager
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.

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, QC Microbiology, Cell Therapy
BMS Netherlands Operations B.V. · Leiden – NL, Netherlands · Associate
Function Therapeutic area Seniority Country
60%
Associate, QC Analytical
BMS Netherlands Operations B.V. · Leiden – NL, Netherlands · Associate
Function Therapeutic area Seniority Country
50%
Quality Assurance Manager Benelux (Rotterdam, NL, 3062 CE)
Perrigo · Rotterdam, Netherlands · Manager
Function Therapeutic area Adjacent seniority Country
50%
QA Manager (Responsible Person Lead) - Team of 3
AbbVie · Zwolle, OV · Manager
Function Therapeutic area Adjacent 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.