Pfizer Hiring 2022 B.Pharm/ M.Pharm/M.S (Pharmacy)/M.Sc/BE or any equivalent for Associate -Validation At India – Vizag. Pfizer Notification full details below..Interested and eligible candidates can Apply Now.Pfizer careers are like no other. In our culture of individual ownership, we believe in our ability to improve future healthcare, and potential to transform millions of lives. We’re looking for new talent to join our global community, to unearth new innovative therapies that make the world a healthier place.
Vacancy details:
- Post Name: Associate -Validation
- Qualification: B.Pharm/ M.Pharm/M.S (Pharmacy)/M.Sc/BE or any equivalent
- Experienced:2+ years of experience in quality assurance and /or validation function of sterile dosage form facility.
Job Description: Pfizer Hiring For Associate -Validation !
Important Details :
- Post of date:03/08/2022
- Location: India – Vizag
- Selection Process: The selection will be on the basis of Interview.
Roles and Responsibilities
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.
Determine process capability of new equipment through execution of approved protocols and assure defined parameters are incorporated into respective operating procedures and batch records.
Assists with development of validation protocols and manage Regulatory queries and responses.
- Participate in deviation investigations to identify root causes and define corrective and/or preventative actions.
- Adhere to all company and Good Manufacturing Practices {also cGMP} procedures, along with safety regulations within the plant and participates in developments of validation programs as needed to remain current with cGMPs and industry.
- Work effectively as a member of the Quality Operations (QO) Good Manufacturing Practices {also cGMP} training team as well as directly with Business Area Training Leads / Coordinators and SMEs within Quality to support Good Manufacturing Practices {also cGMP} and site training initiatives.
- Report to the Validation Section Manager, the Validation Engineer will assure that equipment, facilities, and utilities are validated in accordance with {Current} Good Manufacturing Practices {part of GxP} principles, regulatory requirements, and company policies and standards.
- Work on summarization of data into concise reports that is reviewed by the QO product professional and approved by production and quality management.
- Define problems, collect data, establish facts, and draw valid conclusion.
- Work in a team environment to meet all team objectives and communicate progress on scheduled projects.
- Understanding of pharmaceutical manufacturing, packaging, quality assurance operations.
- Knowledge of validation principles and practices related to the following areas: manufacturing process, analytical method, cleaning methods, facility, equipment, instrument, utility system, and CSV systems.
- Conversant with design & working principles of key equipment used in sterile manufacturing -autoclave, tunnel, homogenizers, filling machine, filter integrity testing devices.
- Well versed with Terminal process – design, execution and review.
- Good document written skills, with ability to identify issues and recommend actions to identify issues and recommend actions.
How to Apply :
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Step 4.Once logged in, User need to fill the all relevant personal ,educational , Work experience details ,attach resume and submit application form.
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