The QC Laboratory Support Specialist provides essential support to the QC Laboratory to facilitate the analytical testing of finished products, stability samples, and raw materials.
This role ensures compliance with GMP, Health and Safety regulations, SOPs, environmental, and regulatory requirements while meeting customer needs.
Additionally, the specialist provides support to the QC Laboratory Supervisors and Managers as required.
Key ResponsibilitiesDaily washing and maintenance of volumetric glassware and beakers, ensuring sufficient stock availability.
Assisting QC Lab Administrators with labelling and appropriate storage of reagents in solvent stores.
Management and appropriate labelling of waste drums before disposal.
Ensuring waste bins are emptied regularly.
Proper disposal and labeling of discarded samples.
Maintaining adequate stock levels of consumables such as filters and syringes within the laboratory.
Managing the inventory of reference standards, chemicals, reagents, and consumables.
Ensuring the availability of reference standards in the laboratory for analytical testing.
Promoting and maintaining good housekeeping and hygiene standards within the laboratory.
Encouraging a safe working environment and adhering to laboratory safety measures at all times.
Leading by example to ensure tidiness and compliance with GLP/GMP standards.
Keeping QC-related records updated and properly filed.
Undertaking any other duties assigned by the QC Supervisor or Manager.
The above list is not exhaustive and may be subject to change based on the evolving needs of the organization.
Skills and CompetenciesEstablishes strong working relationships and fosters a cohesive team environment.
Displays a positive outlook with strong coaching skills and maintains engagement at all times.
Takes a methodical, systematic, and structured approach to organizing work.
Makes effective and consistent decisions in a timely manner.
Takes personal responsibility for decision-making and taking action within their area of responsibility.
Escalates issues appropriately when necessary.
Takes corrective action on performance issues in a fair and consistent manner.
Displays flexibility, a willingness to succeed, and a proactive approach to tasks.
Qualifications and RequirementsBachelor's degree (3rd level qualification).Strong computer skills, particularly in MS Office.
Experience working within a pharmaceutical cGLP environment, with knowledge of EU GMP and US FDA guidelines.
Good understanding of MSDS and its interpretation.