Thermo Fisher Scientific Inc. is the world leader in serving science, with annual revenue exceeding $25 billion. Our Mission is to enable our customers to make the world healthier, cleaner and safer. Whether our customers are accelerating life sciences research, solving complex analytical challenges, improving patient diagnostics and therapies or increasing productivity in their laboratories, we are here to support them. Our global team of more than 75,000 colleagues delivers an unrivaled combination of innovative technologies, purchasing convenience and pharmaceutical services through our industry-leading brands, including Thermo Scientific, Applied Biosystems, Invitrogen, Fisher Scientific, Unity Lab Services and Patheon. For more information, please visit www.thermofisher.com.

Location/Division Specific Information

The Groningen site is a multi-product and multi-client biopharmaceutical site with development and manufacturing facilities for pharmaceutical products for clinical trials (phase 1, 2 and 3) and commercial production.

How will you make an impact?

Through this role you will be responsible for reviewing, creating and updating critical documentation for the Operations department. You will work in cross-functional teams to support timely delivery of a wide array of documents that will directly impact clients and a multitude of departments within the organisation.

What will you do?

• Production Protocols

• Change Controls

• SOPs

• PV Protocols

• PPQ Protocols

What do you have?

• Minimal level High School diploma in combination with industry experience; Masters + in relevant field with no industry experience.

• 1 year of relevant experience in Biotechnology or related field.

• Good knowledge and working in cGMP environment.

• Good knowledge of Upstream and Downstream processes, excellent Microsoft word skills.

• You are cooperative, disciplined, driven and reliable.

• Integrity is one of your personal key values.

• Accomplished in planning and organizing.