Job Title:
Quality Control Reference Material Specialist
About the Role:
* Support digital systems to manage reference materials and critical reagents.
* Manage digital systems to pull and analyse data for the QC laboratories.
* Perform statistical analysis to evaluate QC critical reagents.
* Manage the automation of statistical digital systems to generate control charts.
* Liaise with customers both internal and external to Pfizer to support overall reference material and critical reagent data management.
* Support qualifications/re-qualifications of reference material and critical reagents in conjunction with Grange Castle QC laboratory teams and within an IMEX framework.
* Drive introduction of new technologies into the reference materials team to support supply of reference materials and critical reagents to internal and external customers.
* Liaise with external contract sites to coordinate testing results for Re-valuations of current lots and the qualification of new lots.
* Support opportunities for Continuous Improvement and embrace Pfizer's culture to own and drive any activities associated with delivering these improvements.
* Implement and adhere to appropriate levels of cGMP within the team and promote safety awareness and the established culture of incident and injury free within the area.
* Perform and assist in additional duties as may be directed by QC Manager.
About You:
* B.Sc. degree in biological/chemical sciences, statistics, computer or other related technical degree or equivalent experience in a regulated industry.
* Minimum of 2 years working experience in a digital support role in the Pharmaceutical/Biotech industry or equivalent environment.
* Excellent communication and interpersonal skills.
* Proven success in proactive project management.
* Experience in managing multiple projects and reporting regularly to management within the organisation.
* Proven ability to communicate problems and required resolution in a positive and proactive manner.
* Self-directed, self-motivated with a demonstrated record in project accountability.
* Demonstrated success in networking across sites/functional teams both internal and external to site.
* Ability to work independently, as well as a member of a team in a dynamic, fast-paced environment.
This is an exciting opportunity to join a world-class facility, dedicated to bringing therapies to the market that will significantly improve patients' lives.