Teva Pharmaceuticals Posted July 31, 2026

Quality Assurance Sr Specialist [Operations Support]

Zejtun, Malta Type not listed
Quality Senior
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Teva Pharmaceuticals has closed or removed this posting -- see current similar openings below.

View the original listing (may no longer be live).

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

This section is where we attract the attention of potential candidates and sell the role. How has the role come about? What makes it appealing? What are the key responsibilities? How is the role better with Teva than with another company? Wherever possible, we should bring through the essence of our EVP pillars, i.e., we care, we’re in it together, and we make work fulfilling.

How You’ll Spend Your Day

Review and approve/reject printed packaging materials in a timely manner according to the production plan.

Prioritise packaging materials listed in the Exceptions Report and ensure same-day review when entered into SAP.

Review and approve printed packaging material specifications, including Version 1 and non-Version 1 documents.

Sample printed packaging materials upon request.

Compile Certificates of Analysis (CoAs) for printed packaging materials as required.

Prepare Batch Release Certificates (Commercial and Registration), including CoAs, BRCs, and CoCs, prior to Qualified Person (QP) review and within agreed timelines.

Provide clients with commercial batch documentation, including approved certificates, starting material certificates, and manufacturing/packaging batch documentation as specified in Technical Agreements or product specifications.

Coordinate the preparation and distribution of finished product samples, registration documentation, and supporting information required for product registration and business expansion activities.

Act as the primary liaison between clients and internal departments for quality-related queries and requests, ensuring responses are provided within 48 hours.

Perform training on new or updated Standard Operating Procedures (SOPs) and ensure compliance with authorised SOPs at all times.

Maintain and update QA records, databases, and logbooks regularly to support efficient and reliable operations.

Archive and retrieve QA batch documentation, logbooks, and packaging material samples as required.

Participate actively in projects aimed at improving quality assurance processes and departmental performance.

Compile assigned Product Quality Reviews (PQRs) on a monthly basis.

Perform additional duties and responsibilities as required by the departme

Your Skills and Experience

Excellent attention to detail and accuracy.

Strong customer service orientation.

Effective communication and organisational skills.

Proactive, reliable, and hardworking attitude.

Proficiency in Microsoft Office applications.

Ability to work under pressure and meet strict deadlines.

Strong teamwork and collaboration skills.

Also prefered to have;

Diploma-level education.

Experience in quality assurance, pharmaceutical operations, packaging review, or a related field is considered an asset.

Also Good to Have

Salary Range

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
Senior
Function
Quality
Therapeutic area
Not listed
Location
Zejtun, Malta
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 195 comparable Senior Quality roles across 52 biopharma companies.

195Comparable roles tracked
184Currently active
52Companies hiring similar roles
29Countries represented

Salary context

62 of 195 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 · Quality Assurance Senior Specialist - Statistical Sorting · Lilly $18/hr – $35/hr (≈ $37,482–$72,592/yr)
Peer group range $55,037 – $219,500 (median $142,078)

Where these roles are based

Top locations among the 195 comparable roles

United States98
India18
Ireland11
China11
Singapore9
Japan5

+ 23 more countries

Seniority mix

195 of 195 peers have a known seniority level

Senior133
Associate Director41
Principal21

Therapeutic area mix

0 of 195 peers have a known therapeutic area; the rest are genuinely unlabeled, not hidden

No peers with a known therapeutic area yet.

Currently open similar roles

This posting is closed, but here are live openings closest to it -- ranked by similarity, not by how well you'd qualify for them.

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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.

45%
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Function Therapeutic area Seniority Country
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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.