Job Description
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:
1. Execute hands-on U/HPLC testing on a range of products.
2. Conduct dissolution testing.
3. Perform pharmacopeial methods such as IR, Appearance, pH, CU, and water content.
4. Adhere to Good Manufacturing Practice (GMP) standards using a new electronic Quality System.
5. Contribute to the setup of the facility and laboratory, and actively participate in building the LIMS system.
6. 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.
7. Contribute to the creation and review of Plans, Methodologies, Work Instructions, and Standard Operating Procedures (SOPs).
8. Hands-on contribution to building a LIMS system to transition to a paper-free lab.
Essential Requirements:
1. 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.
2. Extensive experience in an analytical laboratory environment with a sound understanding of regulatory requirements.
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