Overview:
We are seeking a motivated and detail-oriented QC Analyst to join our Quality Control department. The QC Analyst will play a critical role in supporting QC laboratory operations, ensuring compliance with GMP standards, and contributing to the quality of manufactured dbDNA and environmental monitoring activities.
Key Responsibilities:
Conduct day-to-day QC testing of raw materials and finished products using molecular biology, microbiology, and biochemistry techniques (e.g., bioburden, endotoxin, gel electrophoresis, pH, HPLC/UPLC).
Perform environmental monitoring of the GMP facility.
Prepare reagents, manage goods and sample receipt, and support procurement and inventory control.
Conduct equipment and instrument verification and maintenance.
Maintain good housekeeping practices in the QC laboratory.
Accurately document all activities to ensure regulatory and quality compliance.
Collaborate closely with other operational departments to support quality and product requirements.
Reporting Line:
The QC Analyst reports to the QC Manager and supports the Head of Quality Assurance in meeting regulatory requirements.
Key Skills & Attributes:
Degree in a scientific discipline (MSc preferred).
Experience in a GMP environment.
Strong understanding of QC processes, preferably with microbiology expertise.
Proficiency with QC techniques, including environmental monitoring, bioburden, gel electrophoresis, and/or HPLC/UPLC.
Practical experience with aseptic techniques.
Self-motivated, organized, and highly accurate with excellent attention to detail.
Ability to work effectively in a fast-paced, compliance-oriented team environment.