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Lupin Walk-in Interview 2025.Lupin Notification full details below.Interested and eligible candidates can attend Interview on scheduled time and venue..

Vacancy details:

Department: Executive – QA/Officer – QA Doc Cell
Eligibility: Bsc/Msc/Bpharm
Experienced :2-10 Years

Important Details :

Location: Pithampur, Indore,
Selection Process: The selection will be on the basis of Interview
Mode of Interview: Face To Face Interview
Interview Rounds of Interview: HR

Job Description: Greetings from Lupin..!!

Hiring for Executive – QA (API exposure) at Lupin Limited.

M. Sc (Chemistry)

up to INR 8.50 LPA

8 to 10 Years

Pithampur, Indore, Madhya Pradesh

Pharmaceuticals

Roles and Responsibilities

Preparation of SOPs of QA, review of other departments’ SOPs.
To perform batch release of API material and review of related documents.
To prepare and review Quality Risk Assessment, Site Master File, Hold Time Study Protocol/Reports, and other study protocols/reports, Specifications, Stability Protocol, and Stability Report Data.
Review of Validation Master Plan.
To review the analytical method transfer protocol/report and method validation documents of the API.
To ensure and handle the investigation of out-of-specification Results, OOT, Deviations, Product failures, and Market Complaints.
To review Quality system documents such as Deviation, Change control, CAPA, OOS, OOT, re-processing, Re-work, market complaints, and market returns.
To review Qualification Protocols/Reports of product, equipment, and facility.
To Review of the Annual Product Quality Review.
To review of Master Document, such as BPR, Test and Calibration Data Sheet, Test Procedures, and Microbiological Test Procedures.
To collect, review, and submit documents to the RA Department for dossier preparation /Regulatory Submission.

Interested candidates can share their resume at [email protected].

Hiring for Officer – QA Doc Cell (API exposure) at Lupin Limited.

  B.Sc. & B. Pharma
  up to INR 5.50 LPA
  2 to 6 Years
  Pithampur, Indore, Madhya Pradesh
  Pharmaceuticals

Roles and Responsibilities

Arrangement of documents and records in documents cell and timely tracking of documents for the effectiveness, submission, retrieval, discontinuation, obsoleting and destruction of the specific documents under the SOP guidance.
Ensure retention of documents and records as per regulatory requirements.
Ensure and monitor the document cell activity as per SOP and facility meets the GMP compliance level.
Preparation and review of Specifications, Standard Test Procedure and Test data sheet such as Raw Material, Packaging Material, In- Process, Intermediate, API Finished and Finished products.
Preparation and review of the SOP’s of Quality Assurance department.
Initiation and review of change control, deviation and other quality system (QAMS system) documents. Tracking of QAMS events for closing and make sure the closure as per timeline.
Issuance, Retrieval and Destruction of documents such as SOPs, Specification and Standard Test Procedure, Logbooks and all other documents.
Documents updating in ‘Omni Docs’ as per SOP.
Master BMR /BPR linking /delinking and printing from SAP.
Preparation of master plan (Master Inspection Characteristic Report) in SAP.
Preparation and review of E-TDS, SAP Annexure’s and related activities i.e. Merging, Uploading, Linking /delinking and Printing in SAP.
E-TDS Merging, Uploading, Linking and Printing in SAP.
Numbering of all type of QAMS document and logging into respective records/system.
To perform the e-DMS Activity such as QA Authorizer.

Interested candidates can share their resume at [email protected].