Intas Pharmaceuticals Ltd-Walk-In Drive for Quality Control / Quality Assurance On 6th Jan’ 2024

Intas Pharmaceuticals Ltd-Walk-In Drive for Quality Control / Quality Assurance On 6th Jan’ 2024

INTAS Pharmaceutical is a leading, vertically integrated global pharmaceutical formulation development, manufacturing, and marketing company. Intas is committed to challenging the unmet medical and societal needs through a comprehensive pharmaceutical value chain spanning across the world.

Walk-In Drive for Quality Control / Quality Assurance On 6th Jan’ 2024 @ Intas Pharmaceuticals Ltd

  • Department: 
  • Quality Assurance: Validation & Qualification (Injectable / OSD) & (Analytical Review) ( Micro & QC)
  • Experience: 2 to 08 years
  • Position: Officer/ Senior Officer/ Executive/ Senior Executive
  • Qualification: B.Pharmacy/ M.Pharmacy/ M.Sc
  • Job Location: Matoda, Ahmedabad
  • Department: 
  • Quality Control : Quality Control & Microbiology -Supervisor/ Analyst
  • Experience: 2 to 08 years
  • Position: Officer/ Senior Officer/ Executive/ Senior Executive
  • Qualification: B.Sc/  M.Sc
  • Job Location: Matoda, Ahmedabad

Date: 6th Jan’ 2024
Time: 09:30 AM to 03:00 PM
Venue: Intas Pharmaceuticals Ltd- Matoda, Plot No. 457, 458 Sarkhej Bavla Highway, Matoda Village, Sanad, Taluka, Ahmedabad, Gujarat 382210

Interested Candidate may share their Updated Resume On – hr_matoda@intaspharma.com

Job Category: pharma
Job Type: Full Time
Job Location: Ahmedabad

Apply for this position

Allowed Type(s): .rtf

About Pharmaceutical Guidanace

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

Check Also

MICROBIOLOGICAL CONTROL FOR EXCIPIENTS, DRUG PRODUCT AND DRUG SUBSTANCE

MICROBIOLOGICAL CONTROL FOR EXCIPIENTS, DRUG PRODUCT AND DRUG SUBSTANCE PURPOSE: To describe microbiological test controls …