Pfizer is Hiring for Associate-CQ Role. All the Candidates who completed B.Pharmacy/ M.Pharmacy are eligible. Interested Candidates can read the following Details and Apply for this role.
Job Description
- Company Name: Pfizer
 - Job Role: Associate-CQ
 - Qualification: B.Pharmacy/ M.Pharmacy
 - Location: Vizag
 - Batch: 2018/ 2019/ 2020/ 2021/ 2022/ 2023
 - Experience: Freshers (0-5 Years)
 - Salary: Up to 6 LPA (Expected)
 
Job Role & Responsibilities
- 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.
 
Eligibility Criteria
- Bachelor’s degree in pharmacy/ master’s in chemistry or pharmacy
 - 0-5 years of experience in quality control testing and sampling
 - 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
 
Preferred Skills
- 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
 
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