Home / Job / Ipca Laboratories Limited – Walk-In Interviews for Production, Quality Assurance Dept. on 01st Aug 2021

Ipca Laboratories Limited – Walk-In Interviews for Production, Quality Assurance Dept. on 01st Aug 2021

Ipca Laboratories Limited – Walk-In Interviews for Production, Quality Assurance Dept. on 01st Aug 2021

Job Description

♦Quality Assurance :

Job Profile: Line Clearance & In-Process checking during Manufacturing & Packing
Designation: Officer/ Sr. Officer
Qualification: B. Pharm/ M. Pharm
Experience: 2-4 years
Section: IPQA

Job Profile: Line Routine In-process check / oversight in Microbiology Laboratory
Designation: Executive
Qualification: B. Pharm/ M. Pharm
Experience: 6-8 years
Section: QMS

Job Profile: APQR / Document Issuance / Batch Release
Designation: Officer/ Sr. Officer
Qualification: B. Pharm/ M. Pharm
Experience: 4-6 years
Section: Documentation

Job Profile: Equipment / HVAC / Qualification, Computer System Validation
Designation: Officer/ Sr. Officer
Qualification: B. Pharm/ M. Pharm
Experience: 4-6 years
Section: Qualification

♦Production/ Tablet: 

Job Profile: Supervision of Granulation activities & Documentation
Designation: Officer/ Sr. Officer
Qualification: B. Pharm/ M. Pharm
Experience: 2-5 years
Section: Granulation

Job Profile: Supervision of Granulation activities & Documentation (Knowledge of FETTE
machine will be preferred).
Designation: Officer/ Sr. Officer
Qualification: B. Pharm/ M. Pharm
Experience: 2-5 years
Section: Compression

Date: 1st August 2021, Time: 10:00 AM to 3:00 PM
Venue: 

Hotel Woodlands, National Highway No. -8, Near Tejpal Motors, Balitha Vapi, Gujarat, 396191.
Contact: Pradeepta Kumar Mohapatra (02606624407).

Apply for this position

Allowed Type(s): .pdf, .doc, .docx

About Pharmaceutical Guidanace

Mr. Shiv Kumar is the Author and founder of pharmaceutical guidance, he is a pharmaceutical Professional from India having more than 14 years of rich experience in pharmaceutical field. During his career, he work in quality assurance department with multinational company’s i.e Zydus Cadila Ltd, Unichem Laboratories Ltd, Indoco remedies Ltd, Panacea Biotec Ltd, Nectar life Science Ltd. During his experience, he face may regulatory Audit i.e. USFDA, MHRA, ANVISA, MCC, TGA, EU –GMP, WHO –Geneva, ISO 9001-2008 and many ROW Regularities Audit i.e.Uganda,Kenya, Tanzania, Zimbabwe. He is currently leading a regulatory pharmaceutical company as a head Quality. You can join him by Email, Facebook, Google+, Twitter and YouTube

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