Pfizer Validations Associate Vacancy – Pharma Candidates Apply
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Job Title: Associate -Validations – Executions
Location: India – Vizag
Eligbility Criteria:
Preferred Education/ Qualification (Eg. Diploma, Certificates, bachelor’s degree, Master’s Degree, licenses, technical certification)
B.Pharm/ M.Pharm/M.S (Pharmacy)/M.Sc/BE
Experience: 2+ years of experience in quality assurance and /or validation function of sterile dosage form facility.
- Bachelor’s Degree
- Excellent attention to detail and working knowledge of Food and Drug Administration
- Regulations/Guidance, and Good Manufacturing Practices
- Excellent organizational skills, and ability to handle changing deadlines
- Strong communication with written and verbal skills
- Working knowledge of Microsoft Office, especially Excel for evaluation of data
Nice-to-Have
- Technical writing experience
- Pharmaceutical Industry with laboratory process validation experience
- Working knowledge of equipment qualification and calibration specifically for laboratory equipment
How You Will Achieve It
- 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.
Apply Online
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