Associate Compliance Expert
Location: Puurs
Posted: 1 day ago
Application Deadline: 12 October 2023
Contract: 40 hours per week
Function Group: Juridisch
Reference: CXRSP-110166
Are you looking for an exciting pharmaceutical challenge within a compliance department for packaging materials?
Don't hesitate to apply via the website with just a few clicks, or send your CV to [emailprotected]
Key Responsibilities:
1. You will monitor the quality status and projects related to the assigned group of raw materials, packaging components, or critical use materials within the SQA group.
2. You will release inspected packaging components and evaluate deviations regarding packaging components.
3. You are responsible for compiling quality files and following them up, as well as preparing and keeping updated the Quality Agreements, spec sheets, and drawings.
4. You will manage supplier follow-up and evaluate the quality status of suppliers, which may involve preparing the annual audit plan, conducting external audits as SME, periodic quality reviews, or ad hoc assessments for individual issues.
5. You are responsible for establishing and evaluating criteria for supplier assessment.
6. You will maintain contact with suppliers regarding quality and technical support information.
7. You will conduct screening/supplier evaluations of raw materials and/or packaging components and follow them up.
8. You are also responsible for ensuring that suppliers take the appropriate actions to maintain control over processes to guarantee good and consistent quality of delivered goods.
9. You will follow up on corrective actions in response to quality deviations, complaints, or observations during audits.
10. You will coordinate periodic status meetings regarding the monitored projects or quality status of the assigned suppliers.
11. You will actively contribute to the ISO 14001 quality system.
12. You will evaluate deviations within the imposed time limits to ensure the continuity of production activities.
13. You will coach and train processes/systems/procedures & high-level coordination and ad hoc project follow-up of “junior” SQA engineers (if applicable).
Your Profile:
* Scientific education in a biomedical, biopharmaceutical, or life sciences direction.
* Experience in a pharmaceutical environment.
* Experience in quality control.
* Team player with good communication and interpersonal skills.
* Disciplined personality with a keen eye for detail.
* Proficient with related software.
* Languages: Dutch and English.
Our Offer:
In addition to your gross salary, as a consultant, you will also receive many fringe benefits such as:
* Meal vouchers of €7.
* Net expense allowance of €80 (tax-free!).
* Hospitalization insurance.
* Car + fuel card (under conditions) OR reimbursement for commuting.
* 32 vacation days.
* 13th month.
* Group insurance.
* ECO vouchers.
Furthermore, Randstad Professionals offers a range of training opportunities to ensure your expertise can continue to grow, and as a consultant, you are regularly welcome at fun Randstad events.
At Randstad Professionals, we have something for everyone: we work via consultancy with short and long projects, but also with permanent contracts and assignments as a freelancer.
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