Thursday , October 22 2020
Home / Job / Mankind Pharma Limited – Urgent Openings for Microbiology / Lab QA Microbiology

Mankind Pharma Limited – Urgent Openings for Microbiology / Lab QA Microbiology

Mankind Pharma Limited – Urgent Openings for Microbiology / Lab QA Microbiology 

Microbiology Officer/ Senior Officer (4 To 6 Years) @ Mankind Pharma

Note: Candidates must have exposure of Pharma manufacturing (USFDA, MHRA, EU) approved organization.    

Sterile Injectable exposure is mandatory for the position.

  • Should have experience in QC as Microbiologist 2 to 6 Years

  • BET, MLT Sampling

  • Bioburden Testing, Water Analysis

  • Environment Monitoring sterile manufacturing Facility-Critical area, controlled area, microbiology laboratory

  • Possess sterile exposure

Sr. Officer / Executive – LAB QA Microbiology

Note: Only USFDA / MHRA / EU approved plant candidates can apply for the position. 

Experience: 5-8 yrs

Sterile Injectable exposure is mandatory for the position. 

– Preparation/review of Specifications, SOP’s, STP’s, GTP’s, Protocols, Reports, Log Books, Calibration records, Analytical Data and Other documents related to QC
– Maintain the record of Microbiological analysis.
– Review of Environmental Monitoring records, MLT, water and media documents.
– Review of method validation documents and instrument, equipment qualification documents.
– OOL, Change control and deviation initiation, investigation and proposal and implementation of CAPA.

Send CV to recruitment.paonta@mankindpharma.com

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

Check Also

QUALITY SYSTEMS MODEL (Resources)IN PHARMACEUTICAL INDUSTRY (Part – II)

QUALITY SYSTEMS MODEL The goal  is to describe a model for use in pharmaceutical manufacturing …