Quality Assurance - Sterility

​Quality Assurance – Sterility

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 quality assurance professional with a focus on sterility on the facility. As such, bringing in an understanding of aseptic processing and contamination control strategies will be essential.

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.

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:

• Experienced Microbiology professional through either education or experience – ideally both

• 5+ years experience in a drug manufacturing environment, specifically aseptic

• Previous QC experience is an advantage

• GMP experience is essential – ideally understanding of regulations across national and US standards

• 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, microbiology, sterile, aseptic, gmp, manufacturing, regulations, cdmo, development, vendor, services,