job title: Associate - CQ(Pfizer)

Roles and Responsibilities

What You Will Achieve

In this role, you will:

• Perform various tests such as water analysis, Limit Test, instrumental like HPLC, GC.

• Conduct analyses on finished products, raw materials, and components, including data entry, review, and approval in a computerized database, and generate EMS reports.

• Ensure training records are updated and correctly filed to reflect current testing capabilities.

• Perform sampling and labeling of materials as per defined procedures and verify all equipment and instruments.

• Interpret and evaluate data for accuracy, precision, trends, and potential cGMP impact, recommending appropriate corrective actions.

• 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.

• 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)

• Bachelor's degree or Masters degree in chemistry or Pharmacy with 1-5 years of relevant experience in Quality control department.

• 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

• Proficiency 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) techniques

• Proven track record in leading continuous improvement projects

• Strong knowledge of lean manufacturing principles, six sigma methodologies, and statistical analysis

• 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

Work Location Assignment: On Premise