SRG are recruiting for a QC Scientist to join a highly successful CDMO based in Greater Manchester. Growing rapidly, the business specialises in taking products from discovery, all the way through early-stage trials and to approval.
Due to continued growth and expansion of the business they are seeking to hire a QC Scientist to join their team in Greater Manchester to support the QC testing of products and assisting with Method Development & validation activities.
Key Responsibilities
- Hands-on analysis of products using UPLC/HPLC
- IR identification
- Appearance testing
- pH testing
- Dissolution testing
- Water content analysis
- supporting method transfers, validations and method development activities for assays, related substances/impurities, dissolution and cleaning validation methods.
- Supporting root cause investigations into deviations, non-conformances and out-of-specification (OOS) results, and implementing appropriate CAPAs.
Qualifications & Experience
- Degree in a relevant scientific discipline such as Pharmaceutical Sciences, Chemistry, Biology, or a similar experience within a related field
- Prior experience in a Quality Control role within a GMP pharmaceutical environment.
- Hands on experience with UPLC / HPLC
- Prior experience working with Oral Solid Dose forms & Dissolution testing would be advantageous
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Quality Control Scientist employer: SRG
As a Senior Clinical Trial Manager at our company, you will thrive in a dynamic and collaborative work environment that prioritises innovation and employee development. We offer competitive benefits, a strong focus on professional growth, and the opportunity to work alongside industry leaders in a location renowned for its commitment to advancing clinical research. Join us to make a meaningful impact in the field of clinical trials while enjoying a supportive culture that values your contributions.
