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IPCA Laboratories Walk In On 13th Feb 2021 for Tablet (OSD) / Packing,QA ,QC

pharmawisdomcoin February 9, 2021

IPCA Laboratories Ltd is conducting Walk in drive on 13th Feb 2021 in Packing,QA ,QC. IPCA Laboratories Limited Laboratories Limited is an international pharmaceutical company based in Mumbai, India. Interested and eligible candidates can attend interview on scheduled time and venue. 

Walk in Details :

  • Company Name: IPCA Laboratories Ltd
  • Location :Vapi
  • Post Name: Tablet (OSD) / Packing / Quality Assurance / Quality Control
  • Qualification: B.sc,M.sc,B.tech,12th,ITI,B.pharma,M.pharma,Diploma
  • Experience: 01 to 06 Years
  • No of Vacancies: 40
  • Details of Salary: NA
  • Contact: Prakash Patel ( 9574095554 )
  • Selection Process: Based on interview
  • Time & Venue:13th Feb 2021,Time:10AM to 4PM,Venue:Hotel Woodland,N.H.NO.8,Vapi

Job Description/Skills Required. 

We are looking for Tablet (OSD) / Packing / Quality Assurance / Quality Control for our division in IPCA Laboratories Limited !

1. Officer / Trainee / Technician/ Supervisor Tablet (OSD):

Candidates should be 12th, ITI, BA, Diploma(Mech, Elect.), D.Pharm, B.Pharm, B.Sc., M.Pharm, M.Sc. with minimum 1-6 years of relevant experience in Granulation/ Compression/ Coating/ Documentation (QMS).

2. Jr. Officer /Officer / Sr. Officer – Packing:

Candidates should be B.Pharm, B.Sc., M.Pharm, M.Sc., B.E.(Electronic), Diploma (Mech, Elect.) with minimum 1-6 years of relevant experience in Blister/ CVC/ Cartonater/ Documentation (QMS).

3. Officer/ Sr. Officer Quality Assurance:

Candidates should be B.Pharm / B.Sc. / M.Sc. /M.Pharm/ B.E. (For Validation) with minimum 1-6 years of relevant experience, on IPQA, QMS & Validation of QA activities.

4. Officer/ Sr. Officer – Quality Control:

Candidates should be B.Pharm / B.Sc. / M.Sc. /M.Pharm with minimum 4-6 years only of HPLC , GC, GCMS.

* B.Pharm fresher vacancy for Apprenticeship only for any QA Dept. Only. Apply on www.mhrdnats.gov.in

Experience of WHO (Geneva), UK (MHRA) & USFDA guidelines and exposure to various regulatory audits will be desirable.

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