Teva Pharmaceuticals Posted September 8, 2026

Qualified Person (QP) (Fixed-term contract)

Bucharest, Romania Type not listed
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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

We are looking for an experienced Qualified Person (QP) to join our Quality organization and play a key role in safeguarding patient safety through oversight of GMP compliance, batch certification, and product release activities. This is an exciting opportunity to contribute to a highly regulated environment where quality and excellence are at the heart of everything we do.

What You'll Do

As a Qualified Person, you will be responsible for:

Batch certification and release activities

Oversight of GMP compliance across manufacturing and quality operations

Review and approval of quality events, deviations, investigations, and CAPAs

Supporting regulatory inspections and audit readiness

Driving quality risk management initiatives

Ensuring compliance with applicable regulatory requirements and quality standards

Acting as a key quality partner for cross-functional teams and stakeholders

What You'll Bring

To be successful in this role, you will have:

Strong GMP and regulatory expertise

Solid experience within the pharmaceutical industry

Hands-on experience with batch certification and product release

In-depth knowledge of Quality Management Systems (QMS)

Experience supporting inspections and regulatory audits

Strong understanding of: EU GMP requirements, including Annex 16

Validation and qualification processes

Deviations, investigations, and CAPA management

Data Integrity principles (ALCOA+)

Quality Risk Management (ICH Q9)

Regulatory compliance requirements

Batch release processes

What Makes You Stand Out

You are a quality-focused professional who combines technical expertise with sound judgment and strong decision-making skills. You bring:

High accountability and integrity

Exceptional attention to detail

Strong analytical and problem-solving skills

Resilience and the ability to perform under pressure

A patient-focused mindset

Leadership capabilities and confidence in decision-making

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

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
Not listed
Function
Quality
Therapeutic area
Not listed
Location
Bucharest, Romania
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 1008 comparable Quality roles across 131 biopharma companies.

1008Comparable roles tracked
957Currently active
131Companies hiring similar roles
48Countries represented

Salary context

193 of 1008 peers report a salary range (USD, annualized)

Peers share this role's job function. This posting doesn't list a seniority level, so peers aren't narrowed by seniority either -- the range below may span more levels than usual.

This roleSubject Not listed on this posting
Lowest disclosed · Quality Control Stability Technician · Regeneron Pharmaceuticals, Inc (USA) $19/hr – $30/hr (≈ $39,395–$61,610/yr)
Highest disclosed · Quality Assurance Specialist · Merck KGaA $65,100/yr – $976,000/yr
Peer group range $50,502 – $520,550 (median $136,700)

Where these roles are based

Top locations among the 1008 comparable roles

United States350
Germany54
Ireland53
China53
Switzerland39
France38

+ 42 more countries

Seniority mix

498 of 1008 peers have a known seniority level

Manager160
Senior116
Intern/Fellow/Postdoc60
Associate Director40
Associate39
Director32
Principal23
Senior Director20
Executive/VP8

Therapeutic area mix

2 of 1008 peers have a known therapeutic area; the rest are genuinely unlabeled, not hidden

Vaccines & Infectious Disease1
Respiratory1

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.

40%similar
Novartis Targu Mures, Romania
Same function Same country
40%similar
Novartis Targu Mures, Romania
Same function Same country
25%similar
Lilly Indianapolis, Indiana, United States of America Associate
Same function

Matched on job function only -- seniority, specialty, and location weren't confirmed as aligned.

25%similar
AbbVie North Chicago, IL Director
Same function

Matched on job function only -- seniority, specialty, and location weren't confirmed as aligned.

25%similar
AbbVie Annecy, Auvergne-Rhône-Alpes Senior
Same function

Matched on job function only -- seniority, specialty, and location weren't confirmed as aligned.

25%similar
AbbVie North Chicago, IL Manager
Same function

Matched on job function only -- seniority, specialty, and location weren't confirmed as aligned.

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.

40%
QA Compliance Specialist
Novartis · Targu Mures, Romania · Seniority not listed
Function Therapeutic area Seniority Country
25%
Director, Clinical Quality Assurance
AbbVie · North Chicago, IL · Director
Function Therapeutic area Seniority Country
25%
Associate Clinical Programmer - Clinical Study Data, Risk based Quality Management & Monitoring
Novartis · Barcelona Gran Vía, Spain · Associate
Function Therapeutic area Seniority Country
25%
Associate Director, Quality Assurance (Global Supplier Quality)
Gilead Sciences, Inc. · Foster City, United States · Associate Director
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.