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Work as CQ Associate at Pfizer

Pfizer is the world's premier biopharmaceutical company taking new approaches to better health.  We discover, develop, manufacture and deliver quality, safe and effective prescription medicines to treat and help prevent disease for both people and animals. We also partner with healthcare providers, governments and local communities around the world to expand access to our medicines and to provide better quality health care and health system support.

Post : Associate-CQ

Roles and Responsibilities
• Manage receipt, storage and handling of raw materials, packing materials, in process, finished and stability samples. .
• Ensure training records are updated and correctly filed to reflect current testing capabilities.
• Perform sampling and labeling of materials as per defined procedure and verification of all the equipment / instruments.
• Interpret and evaluate data in terms of accuracy, precision, trends and potential Good Manufacturing Practices {also cGMP} impact and recommend appropriate corrective actions.
• Ensure all documentations and quality records are conducted in accordance to Good Manufacturing Practices and Good Laboratory Practices requirements and that they are filed in accordance to existing policies.
• Review and revise Standard Operating Procedures (SOPs), analytical methods and related procedures/documents, to keep them current.
• Perform analyses on finished products, raw materials, and components including entry, review, and/or approval of data in a computerized database and generate EMS reports.
• Contribute to the completion of complex projects, manage own time to meet agreed targets and develop plans for work activities on own projects within a team.

Candidate Profile :
• 0 to 5 years of experience
• Bachelor's Degree in Pharmacy and master’s in pharmacy, Masters in Chemistry
• Demonstrated technical skills in packing, raw material, In process, stability and finished product 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
• Laboratory work experience with analytical HPLC (High Pressure Liquid Chromatography) technique
• Experience leading continuous improvement projects
• Knowledge of lean manufacturing, six sigma methodologies, and statistics

Additional Information
Qualification : M.Pharm, B.Pharm, M.Sc, B.Sc
Location : Vizag
Experience : 0 to 5 years of experience
Industry Type : Pharma / Healthcare / Clinical research
Functional Area : Quality Assurance and Control
End Date : 30th October, 2022

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