Cipla Ltd Announces Job Vacancy For M Pharma Candidates – Apply Now
Cipla ltd hiring pharma candidates. M Pharma job opening 2022. M Pharma job opening 2022. Candidates with master’s degree in pharma may apply for the job opening at Cipla Ltd. Pharma job opening 2022. M Pharma job opening 2022. Check out all the details on the same below:
Job Title: Formulator (63766)
Job Location Vikhroli, Maharashtra
Division IPD
Department Respiratory-Formulations R&D
Employment Type Permanent
Eligibility Criteria Master in Pharmacy (Specialization in Pharmaceutics)
Relevant Work Experience 4 years experience in R&D (Preferably in Injectables)
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 end to end formula and process development of products following good laboratory practices and continuously monitor its data and quality to have robust a product within the budget, timeline and regulatory standards
Accountabilities
I. Collate and review Pharma literature from USFDA etc. in order to utilize knowledge during product development
II. Provide and submit all stage gates documents to CFT on the basis of data generated from development trials to execute batches at plant
III. Gather data from pre-formulation studies by carrying out characterization of reference product and optimize the formula in order to develop a robust product
IV. Provide indent through supply chain management to procure the Filters, RM and PM required during product development and submission batches
V. Prepare regulatory submission data by conducting R&D trials and executing regulatory submission batches at the unit for successful filing
VI. Provide deficiency response support by generating data at R&D/Unit required for approval of the product
Apply Online
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