Pfizer Inc. is an American multinational pharmaceutical and biotechnology corporation headquartered on 42nd Street in Manhattan, New York City. The company was established in 1849 in New York by two German entrepreneurs, Charles Pfizer and his cousin Charles F. Erhart
Pfizer Walk In
- Qualification: B.Pharma, M.Pharma, B.Sc, MS/M.Sc
- Experience : 01-05+years
- Department: QC
- Job Title: QC Analyst
- Job Location: Ahmedabad/Visakhapatnam
Time and Venue:
28 April , 8.00 AM – 3.00 PM
GINGER HOTEL – GAJUWAKA- VIZAG #27-8-308/1/1 |Sri Ram Nagar|Srinagar|Near Vadlapudi Railway Gate|Vadlapudi|Gajuwaka |Visakhapatnam 530046
Contact – ZABI (HR)
Job description:
- Equipment handling experience:
- Waters HPLC with EMPOWER, GC, IC, UV, IR, Potentiometer, KF, LBPC
- Preferably: Experience on Analytical method validations, method transfers handling of Stability testing for injectable products.
- 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.
- Conduct Microbiological protocols on an as needed basis.
- 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.
Qualifications
Must-Have
- Bachelor’s Degree/ master’s degree
- 1 to 5 Years of relevant Experience.
- 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
Nice-to-Have
- 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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