Pfizer B Pharma & M Pharma Associate Job Vacancy

Pfizer B Pharma & M Pharma Associate Job Vacancy - Apply Online

Pfizer B Pharma & M Pharma Associate Job Vacancy – Apply Online

Pfizer job opening 2022. B Pharma and M Pharma candidates apply for the job opening at Pfizer. Pfizer job opening 2022. B Pharma job oopening 2022. Candidates with bachelor’s degree and master’s degree in pharma may apply for the job opening at Pfizer. Interested and eligible candidates may check out all the details on the same below:

Job Title: 600469 – Associate Validations

Location: India – Vizag

Id: 4862036

Eligbility Criteria:

  • Bachelor’s Degree Pharma/ M.Pharm/M.S (Pharmacy)/M.Sc/BE
  • Understanding of pharmaceutical manufacturing, packaging, quality assurance, and quality control 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, lyophilizers, homogenisers, filling machine, filter integrity testing devices.
  • Well versed with Terminal process – design, execution and review.
  • Experience in plant and QC lab operations
  • Good document written skills, with ability to identify issues and recommend actions.
  • Knowledge of current validation regulations in the industry.
    cGMPs and FDA , MHRA, TGA, MCC etc. regulatory guidelines and validation principles.
  • 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


  • Technical writing experience
  • Pharmaceutical Industry with laboratory process validation experience
  • Working knowledge of equipment qualification and calibration specifically for laboratory equipment

What You Will Achieve

You will be a member of Pfizer’s dedicated and highly effective quality assurance team. You will be responsible for the evaluation, review and approval of the validation master plan, protocols and reports. Your methodological approach will help us ensure compliance of our quality systems with company standards and government regulatory requirements. Your
problem-solving ability will help us troubleshoot validation problems for equipment and performance processes and conduct statistical analysis of testing results and process anomalies. Your documentation skills will guide the writing, review and approval of for validation process documents and technical reports related to equipment, products and processes.

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 conclusions.
  • Work in a team environment to meet all team objectives and communicate progress on scheduled projects.

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