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Are you an experienced QC Analyst looking for an exciting new challenge to help shape the Quality Control Department of a contract pharmaceutical manufacturing organisation?
Job Title: QC Scientist – Analytical Chemistry
Type: Permanent
Salary: Highly attractive with great benefits
Location: Northwest, England
SRG is currently working exclusively with a highly successful, award-winning, contract development and manufacturing organisation, focused on providing expert intelligence and support to their partners, driven by their capabilities.
As a result of rapid expansion, we are looking for a QC Analyst to support the QC department with analytical testing, QC validation and helping set up their new facility.
Typical responsibilities/accountabilities:
* Execute hands-on U/HPLC testing on a range of products.
* Conduct dissolution testing.
* Perform pharmacopeial methods such as IR, Appearance, pH, CU, and water content.
* Adhere to Good Manufacturing Practice (GMP) standards using a new electronic Quality System.
* Contribute to the setup of the facility and laboratory, and actively participate in building the LIMS system.
* Support activities to qualify equipment required for QC testing, ensuring compliance with current European Pharmacopoeia and ICH requirements, and participate in the calibration of analytical equipment as needed.
* Contribute to the creation and review of Plans, Methodologies, Work Instructions, and Standard Operating Procedures (SOPs).
* Hands-on contribution to building a LIMS system to transition to a paper-free lab.
* Educated to Degree level in a relevant scientific discipline along with significant, recent hands-on experience of using HPLC and carrying out dissolutions, within a GMP environment.
* Extensive experience in an analytical laboratory environment with a sound understanding of regulatory requirements.
Seniority level: Associate
Employment type: Full-time
Job function: Analyst, Research, and Quality Assurance
Industries: Pharmaceutical Manufacturing and Biotechnology Research
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