Company
pharmaceutical
SeniorQCChemist
Neural analysis suggests this role is
optimal for Senior candidates.
“Senior QC Chemist. Skills: Quality Control, cGMP, ALCOA principles, Data Integrity, Laboratory Investigations, SOPs, GMP documentation. Review and approval of QC sample/lot disposition in the QC Laboratory. Work with the different QC teams to ensure products are tested and released within the stipulated timeline”
Industry & Context.
Effective problem-solving skills; Use Imex "way of working" for day-to-day operations, problem solving, escalation and continuous improvements
What They're Looking For.
Must Have
Knowledge of cGMPs and ALCOA principles, Knowledge of regulatory requirements and guidelines, Embrace the use of digital technology to scale and speed up every form of interaction and action, Degree in Science (Pharmaceutical Science / Chemistry / Molecular Biology), A minimum of 5 years QC experience in the pharmaceutical industry
Nice to Have
Experience in gLIMS/SAP
What You'll Do.
Review and approval of QC sample/lot disposition in the QC Laboratory
Work with the different QC teams to ensure products are tested and released within the stipulated timeline
Conduct and support laboratory investigations
Author annual LIR trend report and Annual Product Record Review (APRR)
Represent QC to participate in monthly EHS safety meeting and be the QC lead to drive the safety culture in QC laboratory
Set up and maintain QC processes (e. g. Sample lot disposition
reference standard and retention samples management)
Author SOPs other GMP documentation
Use Imex "way of working" for day-to-day operations
escalation and continuous improvements
Perform quality review of completed Laboratory Information Management System (gLIMS) test records ensuring strict adherence to ALCOA principles and Data Integrity (DI) requirements
Perform Approval of QC samples/Lot disposition in the gLIMS and release of API
solvents and packaging materials
Ensure prompt approval of QC samples as per Service Level Agreement for the different products and escalate any potential delay to the different functions
Conduct laboratory investigations regarding testing
reference standards and API release where required and ensure all follow-up actions are completed
Collaborate with internal stakeholders and author annual LIR trend report and Annual Product Record Review (APRR)
Represent QC in New Product transfer meeting to ensure all operational issues noted are escalated and resolved
Represent QC to participate in monthly EHS safety meeting and be the QC lead to drive the safety culture in QC laboratory
Lead and maintain 5S culture
practice good housekeeping and ensuring all safety procedures are followed
Perform change management activities if required
Provide guidance and support fellow teammates in the management of retention samples
laboratory chemicals and supplies in accordance to site SOPs
Author SOPs and other GMP documentation
Conduct training for fellow colleagues
Uphold Pfizer's code of conduct and values
Lead continuous improvement activities and collaborate with cross-functional teams to drive flawless execution
Play an active and impactful role in Tier processes by updating performance against metrics
with appropriate escalations
Support development and implementation of solutions
How You'll Work.
Team & Collaboration
Work with the different QC teams; Collaborate with internal stakeholders; Represent QC in New Product transfer meeting; Represent QC to participate in monthly EHS safety meeting; Provide guidance and support fellow teammates; Collaborate with cross-functional teams
Communication Scope
Demonstrated leadership and interpersonal communication skills
Process & Methodology
Effective planning, organization and time management skills, Lead continuous improvement activities
Full Job Description
**Use Your Power for Purpose** Every day, our unwavering commitment to quality ensures the delivery of safe and effective products to patients. Our flexible, innovative, and customer-oriented culture is rooted in science and risk-based compliance. Whether you are engaged in development, maintenance, compliance, or research analysis, your contributions have a direct impact on patient care. By being part of our team, you help uphold a quality culture that adapts and evolves to meet the needs of patients, ensuring that every product we deliver meets the highest standards of safety and efficacy. **Position Summary** The incumbent is a member of the Quality Control (QC) Laboratory team. Under the supervision of the QC Manager / Supervisor, the key responsibilities are: * Review and approval of QC sample/lot disposition in the QC Laboratory. * Work with the different QC teams to ensure products are tested and released within the stipulated timeline. * Conduct and support laboratory investigations. * Author annual LIR trend report and Annual Product Record Review (APRR). * Represent QC to participate in monthly EHS safety meeting and be the QC lead to drive the safety culture in QC laboratory. * Set up and maintain QC processes (e.g. Sample lot disposition, reference standard and retention samples management). Author SOPs other GMP documentation * Use Imex "way of working" for day-to-day operations, problem solving, escalation and continuous improvements. **What You Will Achieve** In this role, you will: * Perform quality review of completed Laboratory Information Management System (gLIMS) test records ensuring strict adherence to ALCOA principles and Data Integrity (DI) requirements. * Perform Approval of QC samples/Lot disposition in the gLIMS and release of API, intermediates, raw materials, solvents and packaging materials. * Ensure prompt approval of QC samples as per Service Level Agreement for the different products and escalate any potential delay to the different
Applying for this Senior QC Chemist role?
Most applicants get filtered before a human reads their resume. See if yours makes the cut.
How to Apply on Workday
- Workday has a multi-step form — save your progress after every section.
- "Apply With LinkedIn" can fail or lose data; manual entry is more reliable.
- Watch for the "Submit for Review" final step — hitting "Save" alone does not submit.
- Job requisition numbers are useful when following up with HR by email.
ANONYMOUS · UNFILTERED
What do employees actually say about this company?
Real rants from real employees. Read before you apply.