Associate-cq

4 weeks ago

Visakhapatnam, India Pfizer Full time

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 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
- Having experience on handling of change controls through Quality tool.
- Preparation of calibration records and Qualification protocols.
- Coordinated with all departments and completed related documentation work in time.
- Initiation of change control and co-ordinate with other departments for Approval and Closing Activity.
- Initiation and closure of change control action items.
- Training shall be provided to the external vendors.
- Follow GDP, cGMP and Safety rules.
- Retrieval, Receiving of SOPs,, Calibration records and Qualification records.
- PHP tools

**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
- 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

LI-PFE

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