What will your job be
As QA Specialist you will provide support of global quality & compliance strategy for commercialized pharmaceutical products with global or multiregional scope. Your responsibilities include:
- Serve as product quality and compliance contact person during planning and execution of major changes of commercialized global products (e.g. product remediations, alternative supplier qualifications etc.)
- Provide product quality and compliance leadership to stakeholders
- Provide expert knowledge of global regulations and guidances and contribute to the final decision-making process
- Drive the application of risk management principles for proactively identifying compliance risks and preparing decisions
- Liaise with regional organizations and ensure proper communication and alignment for divisional driven product quality and compliance initiatives
- Promote innovation and continuous improvement
What are we looking for
For this position as QA Specialist we are looking for a candidate who recognizes him- or herself in the following profile:
- BSc or MSc degree in Chemistry, Pharmacy, Biology, Microbiology,or other relevant scientific area
- Minimum 3+ years QA experience in a Pharmaceutical manufacturing environment
- Knowledge of international and local quality system and compliance legislations and standards
- Ability to use Quality Risk Management tools.
- Troubleshooting and issues resolution skills and project management expertise
What do we offer
- A contract for 12 months at CheckMark, with the possibility of an extension
- Salary indication from €4000,- gross per month based on a full-time position
- Full-time position, where 32 hours a week is negotiable
- Dayshift
Where will you work
An international pharmaceutical company in Deventer. You will be part of the Operations Quality and Compliance department, which has a global focus.
More information
Jurjen Wilschut