Cipla Ltd Pharma QC Team Member Vacancy 2022 – Apply Online
Cipla Ltd job opening 2022, Quality control job vacancy 2022. Pharma job opening 2022, MSc job opening 2022. Candidates with a bachelor’s degree in pharmacy may apply for the team member QC job vacancy. Intrested and eligible candidates may check out all the details on the same below:
Job Title: Team Member_QC (65140)
Job Location Goa
Division Quality
Department Quality
Employment Type Permanent
Education Qualification M.Sc. / B. Pharma
Relevant Work Experience 1-3 years of experience in QC department of a pharmaceutical organization
Competencies/Skills
- Communication Skills (clarity of thought, comprehension)
- Likely potential for growth
- Job / Product / Technical Knowledge / Pharma domain knowledge
- Presentation & Interpersonal skills (If applicable)
- Managerial or People Management skills
- Safety awareness (If applicable)
- Relevance of Previous Experience
- Comprehension, Analytical & Problem-solving abilities
- Productivity & Result Orientation (If applicable)
- Attitude
- Qualification fitment
- Sales drive (If applicable)
- Personality traits (Individualistic / Team player, Outspoken, Maturity level etc.)
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 pharmacopeia 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 documentation to ensure compliance with the current pharmacopeia through consent with the regulatory body
- Review the new/revised monograph as per current pharmacopeia
- Review the latest pharmacopeial updates and monitor its timely implementation to avoid any non-conformances
- Intimate the concerned stakeholders to initiate and complete activities before the effective date of pharmacopeiaEscalate non-conformances timely to avoid any delays in operation
III. Review the assigned documents by referring the concern 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 valid backup documents, SOPs, etc. so that every document is complying 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 entries
• Maintain correct and updated record 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
Click Here To Apply Online
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