Intas Pharmaceuticals Ltd, Experience spanning three decades in healthcare, with a wide range of formulations to meet the needs of ailing humanity, Intas Pharmaceuticals headquartered at Ahmedabad (India), is now a force to reckon with, in the global pharma horizon. With expertise in a range of formulations, from tablets to injectables to newer drug delivery systems, Intas is currently ranked 17th among the Indian Pharma majors.
Intas WALK IN DRIVE AT AHMEDABAD
- Department – QC / Microbiology / QA / IPQA
- Qualification : B.Pharm, M.Pharm, B.Sc, MS/M.Sc
- Experience: 02-07+ years
- Location: Ahmedabad
- No.of Openings: 40
Job Description:
We are hiring multiple positions for our Matoda, Ahmadabad facilities as mentioned below.
Requirement / Designation / Experience / Qualification and Role & responsibilities
A) Quality Control : Officer / Senior Officer
02 to 06 years relevant functional exp.
Qualification: M.Sc. / B. Sc.
Analysis using instruments I.e HPLC, GC, UV, IR, RM/PM/FG/VALIDATION & Stability requirements. Through knowledge on good laboratory practices
B) Microbiologist: Officer – Executive
02 to 06 years relevant functional exp.
Qualification: M.Sc. (Microbiology)
Technical expert for all microbiology functional applications, concerns, issues and decisions in the organization including aseptic techniques and procedures.
C) QA – IPQA/Validation & Qualification and Analytical Review (Injectable/OSD) :
Officer / Senior Officer / Executive / Senior Executive
03 to 09 years relevant functional exp.
Qualification: M.Sc. / B. Pharm / M. Pharm
Process and Cleaning validation, protocol report and risk assessment
Equipment qualication documents (URS, FAT, SAT, DQ, IQ, OQ, PQ) & Compliance mgt.
SME in HVAC validation, Equipment Qualication
In Process Quality Assurance and ensuring the cGMP compliances
A) Quality Control : Quality Control Review
Executive / Senior Executive
04 to 08 years relevant functional exp.
Qualification: M.Sc.
review of the analytical results generated from HPLC, GC, UV, IR, RM/PM/FG/VALIDATION & Stability . Through knowledge on good laboratory practices, analytical method development and validation requirements
-Through knowledge on cGMP norms & Laboratory safety
*Having relevant functional experience in Quality Control / Quality Assurance
– Preference to the candidates with relevant functional experience in Pharmaceutical –
– Preferred age is less than 37 years
– Good communication skills
– Willing to work in shifts
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