Do you have experience in quality assurance under GMP and a strong background in technical writing? Are you looking for a dynamic role in an international and inspiring environment?
Job Description
As a Technical Writer, you will be responsible for investigating deviations, conducting root cause analyses, and implementing CAPAs (Corrective and Preventive Actions) within a cGMP environment. You will collaborate with various departments, including QA, Manufacturing, Supply Chain, and QC.
The primary focus of this role is writing SOPs and addressing comments to ensure compliance and efficiency in procedures.
Responsibilities:
- Monitor timelines for deviations and events while ensuring effective communication between departments.
- Conduct in-depth investigations to identify root causes and propose corrective actions.
- Drive process and procedural improvements.
- Support the team with the submission of change controls, investigations, and CAPAs.
- Review and create SOPs to maintain compliance with regulatory standards.
Requirements:
- Bachelor's degree in Science, Pharma, or Logistics.
- 2-5 years of experience.
- Experience in quality assurance under GMP regulations.
- Strong organizational and problem-solving skills.
- Ability to work in a fast-paced environment and manage multiple priorities.
- Excellent written and verbal communication skills.
Benefits:
- A diverse, challenging role with various QA responsibilities.
- Interaction with multiple departments within a large organization.
- Salary range: €2500 - €3500 per month.
- Long-term assignment.
- Location: Sittard.
- Employment type: Temporary role; until the end of March.
- Language: English.
Would you like to contribute to process improvements in a regulated environment? Apply today!
