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:

Should have strong QC knowledge on the equipment operations and trouble shoot.Should independently operate HPLC,UV,FTIR, Melting point, Autotitrator and all basic QC equipment's.Should have strong analytical skill and capable of handling and method related issues.Very good communication.Flexible to work in different sections in laboratory.Ensure all documentation and quality records comply with Good Manufacturing Practices and Good Laboratory Practices and are filed according to existing policies.Review and revise Standard Operating Procedures, analytical methods, and related documents to keep them current.Conduct analyses on finished products, raw materials, and components, including data entry, review, and approval in a computerized database, and generate EMS reports.Contribute to the completion of complex projects, manage time effectively to meet targets, and develop plans for work activities within a team, while exercising judgment with reliance on supervisor and working under their direction.

Here Is What You Need (Minimum Requirements)

BPharm/ Msc. degree with 2 to 4 yearsDemonstrated technical skills in method validation and testingAbility to read and understand applicable compendial methods, Standard Operating Procedures, technical procedures, and governmental regulationsKnowledge of Good Manufacturing Practices and its application standards, processes, and policies.Excellent organizational skills and strong ability to multi-taskStrong written and verbal communication skillsProficiency with unique Quality Control instruments to meet accuracy specifications for sample management, retains management, interpretation, and evaluation

Bonus Points If You Have (Preferred Requirements)

Experience with laboratory work, particularly using analytical HPLC (High Pressure Liquid Chromatography) techniquesProven track record in leading continuous improvement projectsStrong knowledge of lean manufacturing principles, six sigma methodologies, and statistical analysisStrong problem-solving skills and attention to detailAbility to manage multiple priorities and meet deadlines.Excellent interpersonal skills and the ability to communicate effectively with colleagues at all levelsAdaptability 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.

Quality Assurance and Control

#LI-PFE