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Supports pharmaceutical manufacturing compliance through document management, electronic form conversion, audit response preparation, change control coordination, CAPA and CCF tracking, manufacturing walkthroughs, and process improvement. The role collaborates with cross-functional teams to ensure documentation readiness and timely inspection preparation while maintaining compliance with cGMP requirements.
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Manages enterprise operational excellence and continuous improvement programs across Pfizer. Leads Lean Six Sigma projects, develops performance metrics, oversees governance and resource planning, coaches project teams, facilitates cross-functional collaboration, and implements IMEx initiatives. Maintains procedural documentation for clinical, medical, safety, and regulatory processes, supports audit readiness, delivers Yellow Belt training, and applies statistical analysis, change management, and problem-solving methods to improve operational performance.
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Maintain, troubleshoot, and perform preventive maintenance on laboratory instruments; coordinate vendors for CMC/AMC activities; support commissioning/qualification; manage QC software, spare inventory, TPM, documentation, safety, and GMP/GLP compliance while collaborating across teams.
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 is of the highest standard.
What You Will Achieve
In this role, you will:
Here Is What You Need (Minimum Requirements)
Bonus Points If You Have (Preferred Requirements)
Pfizer is an equal opportunity employer and complies with all applicable equal employment opportunity legislation in each jurisdiction in which it operates.
To learn more about acceptable and prohibited uses of AI during the recruitment process, please review our candidate AI-use guidelines available on Pfizer Careers .
Quality Assurance and Control
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 is of the highest standard.
What You Will Achieve
In this role, you will:
- Responsible to handle breakdown maintenance and troubleshooting of laboratory instrument's/equipment's (Hardware & Software) to ensure all in working condition.
- Perform the Preventive maintenance of laboratory instrument's/equipment's as per schedule.
- Coordinate with the vendors for the maintenance activities for the equipment having CMC & AMC.
- Responsible for other activities related to Quality control which assigned by the Manager/ Supervisor.
- Escalation of analytical issues to next level.
- Responsible for the procurement of new instruments/equipment's as per laboratory requirements.
- Responsible to provide support for Commissioning, Installations and qualifications of Instruments/equipment's.
- Accountable for the TPM (Total productive maintenance) to increase over equipment efficiency.
- Spare Inventory management.
- Quality Control Software data management. (User ID and password management, projects creation and other administrative support works).
- Responsible to handle all Laboratory Safety requirements.
- Co-ordination and communication with cross functional teams and equipment vendors for technical support.
- Preparation of all maintenance related document's (PM procedures, Operator care check list etc.).
- Ensure all documentation and quality records comply with Good Manufacturing Practices and Good Laboratory Practices and are filed according to existing policies.
Here Is What You Need (Minimum Requirements)
- Diploma in Electronics & Instrumentation, B.Sc. Electronics & Instrumentation, M.Sc. Electronics & Instrumentation, B-Tech Electronics & Instrumentation with 1-5 year of experience.
- Demonstrated technical skills in Laboratory equipment/instrument trouble shooting and Preventive Maintenance.
- 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
- Proficiency with unique Quality Control instruments to meet accuracy specifications.
Bonus Points If You Have (Preferred Requirements)
- Handon experience on trouble shooting & Preventive Maintenance of laboratory instrument's/equipment's, particularly HPLC (High Pressure Liquid Chromatography), Gas Chromatography, Titrators, Spectrophotometers, etc.
- Proven track record in leading continuous improvement projects
- Strong problem-solving skills and attention to detail
- Ability to manage multiple priorities and meet deadlines.
- Excellent interpersonal skills and the ability to communicate effectively with colleagues at all levels
- Adaptability and willingness to learn new techniques and procedures
Pfizer is an equal opportunity employer and complies with all applicable equal employment opportunity legislation in each jurisdiction in which it operates.
To learn more about acceptable and prohibited uses of AI during the recruitment process, please review our candidate AI-use guidelines available on Pfizer Careers .
Quality Assurance and Control
Pfizer Chennai, Tamil Nadu, IND Office
Chennai, India
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