Pfizer Singapore is recruiting employees for manufacturing site expansion of PFIZER ASIA MANUFACTURING PTE LTD (PAMPL) in Singapore.
Why Patients Need You
Everything we do, every day, is in line with an unwavering commitment to the quality and the delivery of safe and effective products to patients. Our science and risk-based compliant quality culture is flexible, innovative, and customer oriented. Whether you are involved in development, maintenance, compliance or analysis through research programs, your contribution will directly impact patients.
What You Will Achieve
You will be a member of Pfizerโs dedicated and highly effective quality assurance and control team. Your knowledge of quality control will be helpful to support our quality programs. Your ability to analyze chemical, biological or microbiological products will help us manage our quality. Your contribution to environmental testing, utility monitoring, analytical testing, microbial identification and sterility testing will help Pfizer provide safe drugs to its patients.
Your qualifications of unique Quality Control instruments will help us meet accuracy specifications for sample management, retains managements, interpretation and evaluation. You will also be relied on for establishing requirements for the transfer of methodology from R&D.
As an associate, your focus on the job will contribute in achieving project tasks and goals. Through your domain knowledge and commitment, you will create a collaborative teaming environment for your colleagues.
It is your hard work and focus that will help in making Pfizer ready to achieve new milestones and help patients across the globe.
How You Will Achieve It
Qualifications
Position Summary:
The incumbent is a member of the Quality Control (QC) Laboratory Systems team. Under the supervision of the QC Manager /ย Supervisor (Systems team), the key responsibilities are:ย
ยทย ย ย ย ย ย Perform / review and document analytical testing and results accurately and in accordance to test methods, siteย SOPs and relevant protocols, adhering to ALCOA principles and Data Integrity (DI) requirements.ย
ยทย ย ย ย ย ย Assist in troubleshooting laboratory technical problems and support laboratory investigations.ย
ยทย ย ย ย ย ย Author SOPs, analytical method transfer protocols and reports and other GMP documentation (e.g. trend reports).ย
ยทย ย ย ย ย ย Perform preventive maintenance or calibration of instrumentation as required, undertake housekeepingย responsibilities and follow safety regulations.
ยทย ย ย ย ย ย Set up and maintain QC processes (e.g. reference standard and retention samples management)
ยทย ย ย ย ย ย Use Imex "way of working" for day to day operations, problem solving, escalation and continuous improvements.
Responsibilities:
ยทย ย ย ย ย ย Perform / review and document analytical testing and results accurately and in accordance to test methods, site SOPs and relevant protocols, adhering to ALCOA principles and Data Integrity (DI) requirements.ย
ยทย ย ย ย ย ย Perform / review and document equipment verification and calibration in accordance to procedures.
ยทย ย ย ย ย ย Highlight any abnormalities detected during testing / review and raise laboratory investigations as required.
ยทย ย ย ย ย ย Support laboratory investigations and perform equipment troubleshooting where required.ย
ยทย ย ย ย ย ย Participate in 5S team initiatives and practice good housekeeping, ensuring all safety procedures are followed.
ยทย ย ย ย ย ย Author SOPs, analytical method transfer protocols and reports and other GMP documentation (e.g. trend reports).ย
ยทย ย ย ย ย ย Set up and maintain QC processes (e.g. reference standards and retention sample management), perform investigationsย as required for any associated deviations.ย
ยทย ย ย ย ย ย Conduct training for fellow colleagues from QC and other departments (e.g. Production).ย
ยทย ย ย ย ย ย Uphold Pfizer's code of conduct and values.ย
ยทย ย ย ย ย ย Collaborate with cross-functional teams to drive flawless execution.
ยทย ย ย ย ย ย Play an active and impactful role in Tier processes by updating performance against metrics, highlighting issues, withย appropriate escalations. Support development and implementation of solutions.ย
ยทย ย ย ย ย ย Contribute to the continuous improvement activities in QC laboratory or cross functional teams as nominated.ย โ
โJob Related Requirements:
ยทย ย ย ย ย ย Effective problem solving skills.ย
ยทย ย ย ย ย ย Demonstrated ability to perform in a team.
ยทย ย ย ย ย ย Knowledge of cGMPs and ALOCA principles.
ยทย ย ย ย ย ย Possess a can-do/pride to succeed attitude.
ยทย ย ย ย ย ย Embrace the use of digital technology to scale and speed up every form of interaction and action.
Must-Have
ยทย ย ย ย ย ย Bachelor's Degree in Science
ยทย ย ย ย ย ย Demonstrated technical skills in method validation and testing
ยทย ย ย ย ย ย Ability to read and understand applicable compendial methods, Standard Operating Procedures, technical procedures, and governmental regulations
ยทย ย ย ย ย ย Knowledge of Good Manufacturing Practices and its application standards, processes and policies
ยทย ย ย ย ย ย Excellent organizational skills and strong ability to multi-task
ยทย ย ย ย ย ย Strong written and verbal communication skills
Nice-to-Have
ยทย ย ย ย ย ย A minimum of 1 year QC experience in an analytical laboratory is preferred.ย
ยทย ย ย ย ย ย Laboratory work experience with analytical HPLC (High Pressure Liquid Chromotography) Technique
ยทย ย ย ย ย ย Experience leading continuous improvement projects
ยทย ย ย ย ย ย Knowledge of lean manufacturing, six sigma methodologies, and statistics
Work Location Assignment: Flexible
Pfizer is an equal opportunity employer and complies with all applicable equal employment opportunity legislation in each jurisdiction in which it operates.
Quality Assurance and Control
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