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 is one of the fastest growing manufacturers of Active Pharmaceutical Ingredients (APIs), Pellets (Semi finished Formulations) and Intermediates.
Our strong commitment of providing quality products is boasted by in-depth industry knowledge, 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 organization in the pharmaceutical industry across India. To cater our customer 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:
- Dates: 20th – 23rd November 2024
- Time: 11:00 AM – 4:00 PM
- Venue:
Sy No.530 and 534, Temple Road, Gummadidala Mandal,
Bonthapally, Sangareddy District, Medak, Telangana State – 502313 - Contact: HR at 8187894455
Details:
- Role Category: Production & Manufacturing
- Industry Type: Pharmaceutical & Life Sciences
- Employment Type: Full-Time, Permanent
JOB DESCRITION:
- Position: Chemist – Production
- Location: Bonthapally, Gummadidala, Hyderabad
- Experience Required: 2 – 4 years in API/Bulk Drug Manufacturing
- Qualification: Any Graduate
Responsibilities:
- Follow cGMP guidelines for API production.
- Manage production processes, including bulk drug manufacturing and reactor operations.
- Supervise production activities to ensure compliance with quality and safety standards.
- Troubleshoot technical issues and contribute to process optimization.
Requirements:
- Proven experience in API production, GMP practices, and bulk drug manufacturing.
- Strong knowledge of reactors and production supervision.
- Ability to collaborate with cross-functional teams to achieve production goals
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