Chemistry & Pharma Job @ Cipla Ltd


Cipla Ltd Chemistry & Pharma Job - Candidates Apply Online

Chemistry & Pharma Job @ Cipla Ltd – Candidates Apply Online

Cipla Ltd hiring pharma and chemistry candidates, MSc Chemistry job opening 2022. M Pharma job opening 2022. Pharma job vacancy. M Pharma job opening 2022. Candidates with master’s degree in chemistry and pharma may apply for the job vacancy at Cipla Ltd. Check out all the details on the same below:

Job Title: Respi CoE Analyst (63595)

Job Location Mumbai Central

Division IPD

Department Respiratory Formulations R&D

Employment Type Permanent

Education Qualification M. Sc. (Analytical Chemistry) / M. Pharm

Relevant Work Experience

2-4 years of experience in a pharmaceutical organisation with knowledge of handling instruments like HPLC, GC, Dissolution tester and DPI related instruments

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, Out spoken, Maturity level etc.)

Job Purpose

Execute the core method development activities and conduct analysis of routine as well as stability samples to finalize specifications and ensure timely delivery of the product to unit

Accountabilities

I. Develop new analytical methods for the analysis of routine as well as stability samples by following proper GLPs to provide results or information regarding products to formulators

II. Perform maintenance and calibration of lab instruments/equipment to get accurate and reproducible analytical result for proper interpretation

III. Document and interpret the analytical data in a timely manner as per GLP / GMP requirements to maintain records and compliance of regulatory norms

IV. Provide support to units or CFTs for transfer of analytical methods and techniques by visiting and demonstrating them with the relevant analysis to ensure the successful and timely transfer of products

V. Maintain proper safety, GLP, and GMP environment in the workplace to minimize accidents and incidents

VI. Review the analytical requirements and recommend corrections in specifications by coordinating with units and CFTs to ensure smooth operations

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