"Are You Ready for a High-Paying Pharmaceutical Quality Control Job in Goa?"

Cipla Quality Control Job For Pharma – Apply Online Now

Team Member_QC

Posting Date: 8 Jul 2024

Country: India

State: Goa

Location: Goa

Req Id: 85169

Division: Quality

Department: Quality

Employment Type: Permanent

Job Purpose

Prepare, update and review the specifications, SOPs, policy and operating documents for analysis of materials in order to ensure alignment to predefined quality parameters and compliance to respective standards / pharmacopeia and cGMP requirements.

Accountabilities

I. Prepare documents like SOPs, specifications, and non-routine documentation and ensure timely availability across the site to provide support during the analysis

  • Prepare/revise corporate documents like SOPs, general analytical methods, etc. by coordinating with site QC/QA
  • Review the applicable pharmacopoeia and guidelines and make appropriate updates
  • Review instrument calibration data w.r.t. operating documents

II. Review the latest pharmacopeial updates, supplements, and amendments by evaluating the updates required in the available document to ensure compliance with the current pharmacopoeia through consent with the regulatory body

  • Review the new/revised monograph as per current pharmacopoeia
  • Review the latest pharmacopeial updates and monitor its timely implementation to avoid any non-conformances
  • Intimate the concerned stakeholders to initiate and complete activities as per the pharmacopeia
  • Escalate non-conformances timely to avoid any delays in operation

III. Review

the assigned documents by referring to the concerned backup and pre-defined quality procedure to ensure its compliance against the quality requirements

  • Follow the approved procedures and current Cipla policies for review approach by referring to valid backup documents, SOPs, etc. so that every document complies w.r.t. the quality aspect of the product
  • Identify and discuss queries/problems faced during the document review by taking initiatives so that further delay in document completion is avoided

IV. Issue documents to applicable units, by maintaining the record of the same in the issuance record (bound book) so the current version of the common document is available at the unit

  • Issue applicable bound books to units by maintaining the log of the same so the current format is available to record the relevant data
  • Maintain correct and updated records of all the issuance of documents and bound books

V. Execute harmonization and simplification process of documents to reduce complexities in processes and ensure standardized procedures are followed

  • Evaluate and prepare documents for standardization across all units at a site
  • Coordinate with CFTs and check requirements as per existing procedures to simplify the process
  • Provide suggestions and ideas by exploring new possibilities to achieve work simplification

Education Qualification: M.Sc. / B. Pharma

Relevant Work Experience: 1-3 years of experience in the QC department of a pharmaceutical organization

Competencies/Skills

  • Collaborate to Succeed
  • Innovate to Excel
  • Perform with Accountability
  • Lead with Empathy
  • Act with Agility
  • Strong Domain Knowledge
  • People Management

Job Location: Goa

Interested and eligible applicants can check out all of the details on the same here.

Keywords: Job Posting, Team Member_QC, Quality Control, Pharmaceutical, Goa, Employment, Permanent, SOPs, Pharmacopeial Updates. Cipla Quality Control Job For Pharma – Apply Online Now. Subscribe to Rasayanika for the latest chemistry and Pharma job openings, follow us on Facebook and Telegram and subscribe to our youtube channel for the latest updates on chemistry and Pharma jobs and much more.

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