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:27 February – 28 February
TIME: 9.30 AM – 4.30 PM
VENUE:Metrochem API Private Limited -Unit-IV Plot No 34B,40B, 60B,J.N. Pharma City, Parawada, Visakhapatnam, Andhra Pradesh 531021
Contact – HR ( 8187898964 )
EXP:3 – 5 years
Not Disclosed
LOCATION:Parawada, Vizag
Job description
Roles and Responsibilities
- Assist in production planning, scheduling, and coordination with other departments.
- Conduct quality control tests on raw materials, intermediates, and finished products using various analytical techniques such as HPLC, GC, UV Spectrophotometry, etc.
- Monitor and maintain accurate records of production processes to ensure compliance with regulatory requirements.
- Collaborate with cross-functional teams to resolve issues related to productivity improvement initiatives.
- Ensure adherence to safety protocols and maintain a clean working environment.
Role:
PRODUCTION & MANUFATURING -OTHERS
Industry Type:
Pharmaceuticals & Lifesciences
Department:
PRODUCTION , MANUFATURING & ENGINEERING
Employment Type:
Full Time, Permanent
Role Category:
Production & Manufacturing – Other
Education:
Any Graduate
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