Pfizer Healthcare India Private Limited (PHIPL) is a legal entity incorporated under the provisions of the Companies Act, 1956. It is an export-oriented undertaking of Pfizer Inc. We are committed to live our purpose, Breakthroughs That Change Patients Lives’. It is grounded in our commitment to fund programs that provide public benefit, advance medical care and improve patient outcomes. Our belief is, that all people deserve to live healthy lives. This drives our desire to provide access to medicines that are safe, effective, and affordable.Nearly 3000 colleagues put patients first and work every day in various teams that are categorized into five broad functions.
Vacancy details:
- Role: Quality Control (QC) Analyst
- Qualification :B.Sc , B.Pharma, M.Pharma ,MS/M.Sc(Science)
- Experience :1 – 5 years
- Salary: ₹ Not Disclosed
Greetings from Pfizer Healthcare India Private Limited ..!!!!
Important Details :
- Location:Visakhapatnam
- Post of date:20/04/2024
- Selection Process: The selection will be on the basis of Interview.
- Mode of Interview: face to face
- Interview Rounds of Interview: HR
Walkin Interview Details:
- Date:28 April
- Time:8.00 AM – 5.30 PM
- Venue: GINGER HOTEL – GAJUWAKA- VIZAG #27-8-308/1/1 |Sri Ram Nagar|Srinagar|Near Vadlapudi Railway Gate|Vadlapudi|Gajuwaka |Visakhapatnam 530046 (View on map)Contact – ZABI (HR)
Job description
Job Title: QC Analyst roles.
Walk in interview on Sunday, 28th April 2024 at 8:00 AM
Interview Venue: GINGER HOTEL – GAJUWAKA- VIZAG
#27-8-308/1/1 |Sri Ram Nagar|Srinagar|Near Vadlapudi Railway Gate|Vadlapudi|Gajuwaka |Visakhapatnam 530046.
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
ABAC
