Intas Pharma – Walk-In Interviews for Manufacturing / QC / Microbiology / QA / IPQA / AQA / Packing / Data Integrity Cell / Compliance Departments on 26th Feb’ 2023

Intas Pharma – Walk-In Interviews for Manufacturing / QC / Microbiology / QA / IPQA / AQA / Packing / Data Integrity Cell / Compliance Departments on 26th Feb’ 2023

Walk-In Interviews for IPQA/ QA/ AQA / QC/ Microbiology/ Manufacturing/ Data Integrity Cell/ Compliance Dept. On 26th Feb’ 2023 @ Intas Pharmaceuticals Ltd

Department: Data Integrity Cell (Formulation )
Position: Executive to Assistant Manager
Qualification: M.Pharm/ M.Sc/ B.Pharm
Experience: 05 to 8 years
Experience in All possible Data Integrity, EBMR, Document, Logbooks, Handling of paper, Audit Trail vs actual execution at site.
Having Good Regulatory audit exposure.

Department: 21CFR Part 11 Compliance (Formulation )
Position: Executive to Assistant Manager
Qualification: M.Pharm/ M.Sc/ B.Pharm
Experience: 05 to 8 years
To Check compliance to 21CFR – instruments and equipment, Activation of policy, Periodic Audit trail review & all which is related to 21 CFR part 11.

Department: IPQA Parenteral & Solid Manufacturing & Packing
Position: Officer to Executive
Qualification: B.Pharm/ M.Pharm
Experience: 2 to 8 years
Experience in IPQA Parenteral & Solid Manufacturing & Packing

Department: QA (Qualification)
Position: Officer to Executive
Qualification: B.Pharm/ M.Pharm/ B.Tech
Experience: 2 to 8 years
Experience in Qualification/ Validation Section in QA Parenteral Manufacturing

Department: Analytical Quality Assurance (AQA)
Position: Senior Officer to Senior Executive
Qualification: B.Pharm/ M.Pharm/ M.Sc
Experience: 5 to 8 years
Experience in AQA (Analytical Quality Assurance )
The person who should have experience in instruments ie. HPLC and others along with exposure of softwares like Chromeleon and LIMS.

Department: Quality Control (Chemical ) & Microbiology Section
Position: Officer to Executive
Qualification: B.Pharm/ M.Pharm/ M.Sc (Organic Chemistry)/ M.Sc (Micro)
Experience: 3 to 5 years
Experience in Chemical / Microbiology Section – As an Analyst/ Finished/ Stability & Knowledge of Instrument – HPLC / GC/ DISSOLUTION / AMV. Sterility, BET, Environment Monitoring Testing.

Date: 26th Feb’ 2023
Time: 09:00 AM to 03:00 PM
Venue: 
Chandigarh: Hotel Solitaire, SCO. 902- 903, Housing Board Chowk NAC, Manimajra, Chandigarh -160101
Vadodara: Hotel Fern Residence, Near Central Bus Depot., Station Road, Vadodara- 390002

Job Category: pharma
Job Type: Full Time
Job Location: - Vadodara Gujarat

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Allowed Type(s): .rtf

About Abha Maurya

Ms. Abha Maurya is the Author and founder of pharmaceutical guidance, he is a pharmaceutical Professional from India having more than 18 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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