Quality Compliance Associate

Teva Pharmaceuticals; Amsterdam; On-site; EUR 60,000 - 90,000; Full time

Job summary

Teva Pharmaceuticals in Amsterdam is seeking a Quality Compliance Associate to support the site's Quality Systems & Compliance team, ensuring cGXP adherence and robust data integrity across processes. You will manage vendor qualifications and assist in inspection readiness within a multinational pharma setting.

The role requires a strong background in pharmaceutical quality, with cross-functional collaboration across departments, and fluency in English; Dutch is a plus.

Qualifications

• University degree in Pharmacy, Chemistry, or related field, or HBO+ with quality industry experience.
• Proven experience with pharmaceutical processes, quality systems, and cGXP requirements.
• Familiarity with process automation in regulated environments; strong data integrity knowledge.
• Ability to translate SOPs and quality requirements into day-to-day operations.
• Experience supporting inspections and audits; cross-functional teamwork.

Responsibilities

• Prepare and support department policies aligned with Teva and site policies.
• Coordinate and implement Teva standards and procedures at the site.
• Ensure compliance with national and international cGXP quality standards.
• Organize vendor evaluation and maintain their qualification status.
• Support inspection preparation and front/back office during inspections.
• Use analyses to identify root causes and determine CAPAs.
• Ensure Data Integrity awareness and lead Data Integrity projects.
• Maintain permanent inspection readiness across the site.

Skills

Quality systems

cGXP compliance

Data integrity

Vendor qualification

Inspection readiness

Cross-functional teamwork

English fluency

Education

University degree in Pharmacy

HBO+ level qualification

Tools

QMS software

Regulatory databases

Job description

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.

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.

EOE including disability/veteran