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Officer/Senior Officer/Executive

2-7 Years
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Job Description

Role & responsibilities :

  • Supervise sterile manufacturing processes such as compounding, filtration, filling, and sealing of injectable products.
  • Ensure compliance with cGMP, FDA, and other regulatory requirements in all production activities.
  • Monitor and control environmental conditions in aseptic areas, ensuring cleanroom discipline is maintained.
  • Coordinate with quality control, quality assurance, and engineering departments for production-related activities.
  • Review and maintain batch manufacturing records (BMR), logbooks, and other relevant documentation.
  • Perform in-process checks and ensure timely reporting of deviations and non-conformances.
  • Assist in validation activities including media fill, equipment qualification, and process validation.
  • Train and guide production staff on aseptic techniques, gowning procedures, and SOP adherence.
  • Ensure timely availability of materials, equipment, and manpower for smooth production operations.
  • Participate in internal and external audits and support compliance initiatives.

Preferred candidate profile

  • Education: B.Pharmacy/ M.Sc.
  • Experience: 1-7 years in injectable (sterile) production in a pharmaceutical company.
  • Knowledge of aseptic processing and cleanroom protocols.
  • Familiarity with equipment like autoclaves, vial washers, filling lines, lyophilizers, and isolators.
  • Understanding of documentation and regulatory requirements (e.g., USFDA, EU GMP, WHO GMP).

More Info

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Function:
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Open to candidates from:
Indian

About Company

Intas is one of the leading multinational pharmaceutical formulation development, manufacturing, and marketing organization in the world. It has been growing at 19% CAGR and crossed the $2.5 billion mark in the past financial year. The company has set up a network of subsidiaries, under the name Accord Healthcare in the EU, US, Canada, SA, Australia, APAC as well as CIS & MENA regions. Intas is present in 85+ countries, with more than 70% of its revenue coming from global business.

Currently ranked 6th in the Indian pharmaceutical market, it’s the largest privately owned Indian generic pharma company. Intas has established leadership in key therapeutic segments like CNS, Cardio, Diabeto, Gastro, Urology, Oncology & Animal Health in India. We are among the top 10 generic players in the highly regulated markets of EU, US & UK.

Intas operates 17 advanced formulations, R&D, and distribution facilities, of which 10 are in India and the rest in the UK, Mexico & Greece with the help of our 23,000+ Human Capital. Between them, the facilities are accredited by global regulators such as USFDA, EMA, MHRA, TGA, and others. The company invests 6-7% of its revenues in R&D and has over 10,000 product registrations worldwide with a strategic pipeline of 300+ high-value FTF/FTM, Biosimilars, and NDDS products.

Intas' highly advanced EU-GMP Certified Biopharma division is fueled by a mission to provide affordable “Biosimilars for Billions” across niche segments such as oncology, auto-immune, ophthalmology, nephrology, rheumatology, and hormone-based therapies.

The Plasma Fractionation Unit of Intas Pharmaceuticals is a pioneer in manufacturing plasma-derived therapeutics. It houses a full-fledged R&D lab and a state-of-the-art WHO-GMP-certified manufacturing facility complemented with a GLP-compliant QC lab.

Our values of Innovation, Customer Delight, Ownership & Collaboration, Performance Focus & Care for Society are the driving forces toward excellence.

Job ID: 121671753