QA Specialist
| Branche | Zie onder |
| Dienstverband | Zie onder |
| Uren | Zie onder |
| Locatie | Amsterdam |
| Opleidingsniveau | Zie onder |
| Organisatie | CheckMark |
| Contactpersoon | Zie onder |
Informatie
As a QA Specialist you provide quality assurance support for assigned Third-Party Manufacturers (TPM) and their quality systems to ensure that safe, effective, and compliant products are consistently supplied in accordance with global cGMP and regulatory standards. You will play a key role in ensuring product quality, compliance, and availability within an international manufacturing network. Your responsibilities:
- Support the TPM QA Manager in all quality-related activities for assigned third-party manufacturers
- Coordinate change control, deviations, CAPAs, and complaint trend follow-up to maintain compliance and product integrity.
- Contribute to the implementation of global quality and compliance strategies for commercialized products.
- Plan and support the execution of major product or material changes.
- Participate in QA cross-functional projects and initiatives to improve quality systems and compliance.
- Support inspection readiness and audit activities, ensuring third-party manufacturers meet global regulatory expectations.
- Maintain proactive communication with internal and external stakeholders and travel occasionally to TPM sites to assess and strengthen quality systems.
-
A contract for 12 months at CheckMark
-
Salary indication from €4300,- gross per month based on a full-time position
- 13 month salary
-
Full-time position, where 32 hours a week is negotiable
- Work from the office in Amsterdam with the option to work from home one day per week
For this position as QA Specialist we are looking for a candidate who recognizes him- or herself in the following profile:
- Bachelor’s degree (or equivalent) in a relevant scientific discipline such as Chemistry, Pharmacy, Biology, or Microbiology.
- Minimum of 2 years of QA experience in a Pharmaceutical manufacturing environment
- Solid understanding of pharmaceutical manufacturing for finished dosage forms and related quality systems.
- Experience with change control, deviations, CAPA, and supplier or TPM quality management.
- Strong communication skills, both written and verbal, with the ability to interact effectively across different cultures.
- Analytical mindset with experience in Quality Risk Management and data-based decision-making.
- Possession of a BSN (citizen service number)
Omschrijving
As a QA Specialist you provide quality assurance support for assigned Third-Party Manufacturers (TPM) and their quality systems to ensure that safe, effective, and compliant products are consistently supplied in accordance with global cGMP and regulatory standards. You will play a key role in ensuring product quality, compliance, and availability within an international manufacturing network. Your responsibilities:
- Support the TPM QA Manager in all quality-related activities for assigned third-party manufacturers
- Coordinate change control, deviations, CAPAs, and complaint trend follow-up to maintain compliance and product integrity.
- Contribute to the implementation of global quality and compliance strategies for commercialized products.
- Plan and support the execution of major product or material changes.
- Participate in QA cross-functional projects and initiatives to improve quality systems and compliance.
- Support inspection readiness and audit activities, ensuring third-party manufacturers meet global regulatory expectations.
- Maintain proactive communication with internal and external stakeholders and travel occasionally to TPM sites to assess and strengthen quality systems.
-
A contract for 12 months at CheckMark
-
Salary indication from €4300,- gross per month based on a full-time position
- 13 month salary
-
Full-time position, where 32 hours a week is negotiable
- Work from the office in Amsterdam with the option to work from home one day per week
For this position as QA Specialist we are looking for a candidate who recognizes him- or herself in the following profile:
- Bachelor’s degree (or equivalent) in a relevant scientific discipline such as Chemistry, Pharmacy, Biology, or Microbiology.
- Minimum of 2 years of QA experience in a Pharmaceutical manufacturing environment
- Solid understanding of pharmaceutical manufacturing for finished dosage forms and related quality systems.
- Experience with change control, deviations, CAPA, and supplier or TPM quality management.
- Strong communication skills, both written and verbal, with the ability to interact effectively across different cultures.
- Analytical mindset with experience in Quality Risk Management and data-based decision-making.
- Possession of a BSN (citizen service number)
