About the role
AI summarisedThis is an entry-level QC Specialist Trainee position in a pharmaceutical/biotech company, part of an Attach & Train program. The role involves supporting QC operations including equipment qualification, master data maintenance in Laboratory Execution Systems, and ensuring cGMP compliance.
BiopharmaFull-timeGeneral
Key Responsibilities
- As part of the QC Support Operations Team to provide support for routine QC activities including: Purchasing, qualification/re-qualification of laboratory equipment and computer systems. All other tactical support activities required to support the business needs.
- Execute projects which encompass QC equipment qualification related activities following cGMP requirements.
- Perform data documentation for executed projects following cGMP procedures.
- Support routine management of equipment and reagent master data in Laboratory Execution Systems (LES).
- Perform development, verification and deployment of LES recipes or other QC systems.
- Ensure that data, documentation and laboratory processes are in a constant state of regulatory compliance and inspection readiness.
- Timely resolution of issues, including raising discrepancies, investigations and implementation of CAPAs.
Requirements
- Degree in Chemistry, Microbiology, Biochemistry, Life Science or equivalent.
- 0 - 3 years of related working experience for degree holders or equivalent holders with combination of education and relative work experience is preferred.
- Strong problem solving capability. Able to determine when to escalate issue.
- Ability to organize and plan effectively. Effective resource management.
- Demonstrate good verbal and written communication skills in English.