Technical Writer

Are you an experienced investigator passionate about quality and compliance in a cGMP environment? We seek a Technical Writer – Deviation Investigator to join our leading CMO. In this role, you will be responsible for initiating and leading investigations into process deviations, identifying root causes, and implementing corrective actions to prevent recurrence.

RESPONSIBILITIES

• Conduct investigations of process deviations and ensure root causes are identified.
• Implement corrective and preventive actions (CAPAs) to mitigate recurrence.
• Maintain timely completion of investigations through strong interdepartmental communication.
• Utilize advanced investigational tools to drive high-quality root cause analyses.
• Drive process improvements by recommending and implementing changes in procedures and workflows.
• Assist in submitting change controls, investigations, CAPAs, and other quality-related documentation.

PROFILE

• Education: Bachelor’s degree in Pharmaceutical Sciences, Supply Chain, Engineering, or a related field.
• 5–10 years of experience in Validation or Engineering within a biotechnology company
• 5–10 years of experience in Quality Assurance.

PRACTICALITIES

• Start Date: March (flexible)
• Location: Geleen, Netherlands
• Duration: 6 months, change of extension
• Setup: 100% FTE, hybrid possibilities
• Language: English, Dutch nice-to-have

INTERESTED?

Interviews and offers can happen coming week

If you’re interested in the above description, please apply with your CV today. For further information, please contact Merel van Os at +31 (0)20 20 44 502 or by email at m.vanos @panda-int.com