Pfizer Hiring for Associate – CQ at Visakhapatnam, Andhra Pradesh Full Time

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 Pfizer’s 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

Calibration of Analytical Instruments.

Planning and execution of PRQ of the Instruments.

gLIMS Master data creation for Vizag site.

Instrument Calibration data creation and schedules tracking in the gLIMS-IM System.

New instrument Qualifications and finalizing the assessment form for the calibration frequencies.

Monitoring and reviewing the external calibration services activities and certificates.

Reviewing of PRQ and IOPQ Protocols in PDOC System.

SME for the CQ-Calibration activities.

Supporting for Investigations and CAPA closing.

Qualification of new calibration service providers in Pfizer SMS System.

Providing the trainings to Contingent workers.

Qualifications

Must-Have

Bachelor’s Degree

Demonstrated technical skills in method validation and testing

Ability to read and understand applicable compendial methods, Standard Operating Procedures, technical procedures, and governmental regulations

Knowledge of Good Manufacturing Practices and its application standards, processes and policies

Excellent organizational skills and strong ability to multi-task

Strong written and verbal communication skills

Nice-to-Have

Laboratory work experience with analytical HPLC (High Pressure Liquid Chromotography) technique

Experience leading continuous improvement projects

Knowledge of lean manufacturing, six sigma methodologies, and statistics

Work Location Assignment: On Premise

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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