
Quality Compliance Associate
Job Description
We Are Teva
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
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