Clinical research associate Jobs in Cuxhaven

Responsibilities:

• Provide technical engineering support and act as a Subject Matter Expert (SME) for fermentation, lyophilization, aseptic filling, utilities, and packaging.
• Lead process improvement initiatives, technology transfers, and scale-up projects to enhance reliability, efficiency, and product quality.
• Manage deviations, CAPAs, change controls, and equipment qualification activities (IQ/OQ/PQ) within a GMP environment.
• Resolve complex process or equipment issues by leading root cause investigations and cross-functional taskforces.
• Drive operational excellence while providing technical leadership and mentorship to operational teams.

What You Need to Succeed (minimum qualifications):

• Bachelor’s or Master’s degree in Process Engineering, Chemical Engineering, Bioprocess Engineering, Mechanical Engineering, or related discipline
• Experience in pharmaceutical or biopharmaceutical manufacturing within a GMP regulated environment
• Excellent communication skills with the ability to collaborate across functions and leadership levels

What will give you a competitive edge (preferred qualifications):

• Fluency in English and German
• Experience with GMP manufacturing unit operations
• Proven experience with equipment qualification (IQ/OQ/PQ) and process validation
• Experience leading engineering projects or continuous improvement initiatives

WHAT WE OFFER YOU

• Interesting and varied working environment in a modern and growing global company in the pharmaceutical industry
• Room for initiative and flexibility
• Exciting development opportunities
• Company fitness program
• Meal allowance
• Corporation benefits
• Team events
• Up to 30 days holiday
• Special leave days (wedding, work anniversaries etc.)
• Attractive remuneration according to the company collective agreement incl. Christmas and holiday bonus
• 38 hours/week