CSV Engineer

​CSV Engineer

I am partnering with a truly forward thinking CDMO that takes a genuine people focused approach to employment and sustainability, in an increasingly competitive market. Through this partnership I am delighted to be supporting their hiring plans for Q1 in 2024 across a range of key disciplines.

For this specific hire, they are seeking an experienced CSV professional that will join a growing team in representing Quality Assurance from a CapEx, qualification and wider computer system validation perspective.

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Having made great strides as a business over recent years, this company has developed a strong reputation for creating a purposeful working environment built around flexibility, autonomy and empowerment.

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Working with global pharmaceutical and biotechnology companies, this business offers services from development and analytical testing, through to clinical and commercial manufacturing.

Therefore, if you are an experienced pharmaceutical professional looking for your next challenge, this company offers a rewarding environment in which to take that step.

Experience:

• Experience in pharmaceutical GMP manufacturing setting

• Experience of aseptic or sterile facilities is advantageous

• Ideally 5+ years of experience with Data Integrity and CSV

• Strong QA experience and understanding of change and deviation management

• Appreciation of both EU and US regulatory requirements

• MSc minimum in a relevant life sciences discipline

• Fluency in German and English, spoken and written

This position is being pipelines for hire mid Q1 2024. Please register your interest by applying or contacting Mark Bux-Ryan directly for more information.

Quality, QA, validation, computer, systems, csv, data, integrity, gmp, manufacturing, regulations, cdmo, development, vendor, services, information, technology, IT