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Thursday, August 31, 2023

[New post] Cipla Ltd hiring for API ADL Analyst/Junior Team Member – QC/Chemical Engineer /Junior Operator – Production

Site logo image SWARNALATHA B posted: " Cipla Ltd Walk-in Interview 2023.Cipla Ltd Notification full details below.Intrested and eligible candidates can attend Interview on scheduled time and venue.Cipla, as an organisation has been built brick-by-brick on the foundation of care. Caring For Li" Pharma Job Alert

Cipla Ltd hiring for API ADL Analyst/Junior Team Member – QC/Chemical Engineer /Junior Operator – Production

SWARNALATHA B

Aug 31

Cipla Ltd Walk-in Interview 2023.Cipla Ltd Notification full details below.Intrested and eligible candidates can attend Interview on scheduled time and venue.Cipla, as an organisation has been built brick-by-brick on the foundation of care. Caring For Life has always been and continues to remain, our guiding purpose. Driven by the sAssistant managere purpose, we have extended our presence to 80+ countries providing over 1,500 products across various therapeutic categories in 50+ dosage forms.

Vacancy details:

  • DEPARTMENT:  API ADL Analyst/Junior Team Member - QC/Chemical Engineer /Junior Operator - Production
  • Qualification: M.Sc. Chemistry /M Pharma / PGD/B. Pharma/B.E (Chemical Engineering)/Diploma in Pharmacy / Mechanical Engineering
  • Prior Experience: 2-5 years

Job Description: Greeting from Cipla Ltd !!!!!

Important Details :

  • Post of date:31/08/2023
  • Location: Goa/Karnataka - Bommasandra/sikkim
  • Selection Process: The selection will be on the basis of Interview.
  • Mode of Interview: Face To Face Interview
  • Interview Rounds of Interview: HR

API ADL Analyst

Job Purpose

Provide analytical support to API R&D, Regulatory Affairs, Manufacturing units and other analytical laboratories by method development of raw materials, intermediates and final API in order to ensure the drug development is carried out as per the project timelines and adheres to all regulatory requirements

Accountabilities

I. Provide method development and routine analysis under GLP environment to finalise the specification for standardization of the molecule and for final DMF submission

II. Investigate plant queries like OOS, OOT for quality control of drug substance and products in order to provide corrective actions and check samples for impurities

III. Characterise final API and impurities to prepare the test or working standards for routine laboratory purpose

IV. Conduct the incubation and perform complete analysis of stability samples to conclude the storage, shelf life and packing conditions of the final API

V. Keep track of the latest innovation and applications which can be used with the existing techniques to investigate / resolve critical issues

  • Education Qualification

M.Sc. Chemistry /M Pharma / PGD

  • Relevant Work Experience

Minimum 5 years of experience in pharmaceutical industry with analytical experience

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.)

Junior Team Member - QC

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

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

III. Review the assigned documents by referring the concern backup and pre-defined quality procedure to ensure its compliance against the quality requirements

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

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

Education Qualification

M.Sc. / B. Pharma

Relevant Work Experience

2 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, Out spoken, Maturity level etc.)

Apply online
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