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Senior Executive – Quality Control Vacancy At Lupin Ltd

Lupin Limited is Hiring for Senior Executive – Quality Control and has issued notification to accept Applications. Lupin Limited is an Indian multinational pharmaceutical company based in Mumbai, Maharashtra, India. It is one of the largest generic pharmaceutical companies by revenue globally. Interested and eligible candidates required to fill  application form in online with Education and personal details and submit application along with resume. Application form link provided at the end of post. Eligibility for the Senior Executive – Quality Control as follows.

Vacancy summary details :

  • Company Name: Lupin Limited
  • Location : Visakhapatnam
  • Post Name: Senior Executive – Quality Control
  • Qualification: B.Sc in Chemistry,MS/M.Sc(Science) in Chemistry, Any Specialization, Bio-Chemistry, Microbiology, Organic Chemistry
  • Experience: 08-12 Years
  • No of Vacancies: NA
  • Details of Salary:NA
  • Opening date for online Application: 24/03/2021
  • Closing date for online Application : Apply as soon as possible
  • Date of examination: NA
  • Time and Venue :NA
  • Mode of application : online
  • Selection Process: Shortlisted candidates may called for selection process (  Personal interview , Group discussion , etc…,)

Job Description/Skills Required: 


Experience of leading operations of HPLC / GC / LCMS / XRD Section operations in Quality Control laboratory & Planning and supervising daily activities of HPLC / GC / LCMS / XRD Section of QC

1. Capable to lead a team & consistent performer with people management skills2. Successfully leading various analytical sections during the regulatory audits like USFDA, EU, ENVISA, WHO etc. in a leading role and should have working experience at supervisory level, not less than 02-06 years3. Well versed in handling of QC related OOS,OOT, deviation and incidence investigations, Train Staff, Operators and update their capabilities on cGMP, Safety, etc…4. Planning, Implementing, prioritizing the operations and jobs as per Plant requirements w.r.t. Raw Materials, in process materials and Finished Products in coordination with PDL, R & D, Production, Warehouse, Purchase, RA and QA5. Documentation and validation of process and analytical methods as per cGMP norms.6. Responsible from Lab commissioning to improvement of systems and practices.

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