Ajanta Pharma- Interviews for QC / QA / Production / Packing on 2nd Mar’ 2024

Ajanta Pharma- Interviews for QC / QA / Production / Packing on 2nd Mar’ 2024

Ajanta Pharma is a specialty pharmaceutical company dedicated to developing, manufacturing, and marketing quality finished dosages. Committed to serving healthcare needs worldwide, Ajanta produces a comprehensive range of first-to-market products in specialty therapeutic segments, customized for each market it serves.

Position Available: Various positions available in the following departments:

  • Quality Control (QC)
  • Quality Assurance (QA)
  • Production
  • Packing

Designation: Sr. Officer / Officer / Executive / Sr. Executive Technician / Electrician / Associate

Qualification:B.Pharm / M.Pharm/M.Sc/ITI/Diploma

Experience: 3 to 10 years of relevant experience in Pharma OSD (Oral Solid Dosage) or Liquid Oral manufacturing background.

Job Location: Pithampur, Indore, Madhya Pradesh

Date & Day of Walk-In Interview: 2nd March 2024 (Saturday)

Time: 10:00 AM to 04:00 PM

Venue: Ajanta Pharma Limited, 55, 56, 57, ISEZ, Pithampur, Indore, M.P

Requirements for Candidates:

  • Interested candidates are required to bring a copy of their latest resume.
  • Candidates should also provide details of their current CTC (Cost to Company) breakup.
  • Please bring a passport size photograph.
  • Note:

    • Candidates who have already appeared for an interview within the last 6 months will not be eligible to attend the interview.
    • Ajanta Pharma does not seek any payment from candidates for employment opportunities. Please exercise caution while dealing with any agency or person claiming to represent Ajanta Pharma.
Job Category: pharma
Job Type: Full Time
Job Location: Indore Pithampur

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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

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