October 31, 2025

Metrochem API Pvt Ltd was established by Dr. N.V. Rao in the year 2004, with a grand vision of being the “most preferred supply partner to pharmaceutical customers worldwide”. The management aimed to achieve this vision with a clear focus on quality, affordability, and products at Metrochem API Private Limited one of the fastest-growing manufacturers of Active Pharmaceutical Ingredients (APIs), Pellets (Semi-finished Formulations), and Intermediates.

Our strong commitment to providing quality products is boosted by in-depth industry knowledge, a well-qualified team of professionals, as well as hi-tech and advanced infrastructure and as a result, creating mutually beneficial associations for all the parties involved.

Our manufacturing facilities are approved by several international regulatory bodies such as ISO 9001-2015, USFDA, WHO: GMP, Cofepris, and Japanese Accredited, inspected by KFDA authorities, and awaiting certification and moving towards USFDA, EU GMP, MHRA & TGA in 2019. Adapting quickly to the ever-evolving demands, we have emerged as one of the fastest-growing organizations in the pharmaceutical industry across India.

To cater to our customers’ high volume requirements, we have dedicated each of our 6 manufacturing facilities to our 3 core product groups – APIs, Pelletization & Intermediates – reinforced by a well-equipped, centralized Research & Development laboratory.

DATE AND TIME:

DATE:3rd February – 5th February 

TIME: 9.30 AM – 5.30 PM

VENUE:Unit-B, Bonthapally, Plot No. 3 and 4. SY.No.42, Alinagar, Sangareddy District, Medak, Telangana State 5023I9

Contact – HR ( 8187894455 )

EXP:1 – 6 years

Not Disclosed

LOCATION:HYDERABAD

Department – Production

Experience – 2 – 6 years

Roles and Responsibilities

  • Operate and maintain pilot plants, reactors, centrifuges, GLRs, SSRs, dryers, and other equipment involved in API manufacturing.
  • Perform routine maintenance tasks to ensure optimal performance of production lines.
  • Monitor and control process parameters to meet quality standards during bulk drug production.
  • Collaborate with cross-functional teams to troubleshoot issues and implement improvements.
  • Ensure compliance with cGMP guidelines and company policies.

Education

Any Graduate

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