Pfizer Hiring For Associate – Manufacturing Quality 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 team. You will evaluate and review Pfizer’s clinical and commercial batches of drugs. You will make sure that product and process documents match the specifications based on established sampling and statistical process control procedures. Your expertise will help in identifying deviations from established standards, in the manufacturing and packaging of products. In the relevant cases you will approve investigations and change control activities to ensure compliance with configuration management policies.

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 commitment that will make Pfizer ready to achieve new milestones and help patients across the globe.

How You Will Achieve It

Responsible for ensuring operating state of cGMP compliance in Terminal Sterilization, Visual Inspection and Packaging operations.

Maintain regulatory compliance in accordance with cGMP practices

Ensure manufacturing policies and procedures conform to Pfizer standards

Knowledge and hands on experience in reviewing EBR and assessing the impact of AMPs exceptions with technical support/inputs from Sr.Specialist or Supervisor.

Review of Batch reports, and Equipment audit trails

Perform Acceptable Quality level sampling, Inspection and record the results in Batch records for all products

Perform batch start-up and end activities viz. sensor challenge tests, recipe review etc.

Perform random process checks for Terminal Sterilization, Visual Inspection and Packaging

Perform Daily walkthroughs and report observations to the Supervisor.

Perform Equipment breakdown assessments w.r.t to Product Quality and patient safety with technical support/inputs from Sr.Specialist or Supervisor.

Perform CC TV monitoring and report the observations.

Report any non-compliance to the Supervisor

Should have trouble shooting abilities in manufacturing area, which helps the organization to develop, implement and achieve its mission, vision and values.

Qualifications

Must-Have

Bachelor’s Degree

Experience in pharmaceutical industry

Experience in Quality administered systems

Sound knowledge of current Good Manufacturing Practices {part of GxP}

Ability to work in a team environment within own team and interdepartmental teams

Effective written and oral communication skills

Nice-to-Have

Experience at a manufacturing site

Experience of writing and managing deviations

Experience in production batch record review, Enterprise Resource Planning system, investigation of non-conformance, root cause analysis and change control management

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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