Syngene Formulation Development Associate - Apply Online

Syngene Formulation Development Associate – Apply Online

Formulation Development Associate Job. Syngene invites postgraduate Pharma candidates for the post of Formulation Development Associate. Interested and eligible candidates may apply online, Check out all the details on the same below:

Job Title: Senior Research Associate-Formulation Development

Job Location: Bangalore

Department: Pharmaceutical Development

Educational Qualification:

Master’s degree in Pharmacy

Technical/Functional Skills:

  • Should have knowledge of SAP MM- Module
  • Must have Chemical knowledge, hazardous identification, compatibility storage and Safety system requirements.
  • Good documentation and SDS management
  • Ability to handle emergency situations such as chemical spillage, fumes, flammable leak, firefighting etc.,
  • Warehouse and Inventory management
  • Should have good communication skill and Computer skills – MS Office i.e. MS word and Excel

Experience:

1-3 years post qualification

Behavioral Skills:

  • Should have the capability to work in a team and ability to handle demonstrate a good team spirit.
  • While possessing a good ability to follow instruction should also demonstrate innovative in his/her approach, good communication skills.
  • Should be proactive while working on allotted responsibility.

Job purpose

Responsible for execution of development trial batches and GMP batches under the supervision of senior scientists in the team.

Key Responsibilities:

  • Should have hands-on working experience on different solid oral manufacturing equipment (not limited) like RMG, roller compactor, powder blenders, tablet compression machines, Wurster processors, tablet coating machines, capsule filling machines, spray dryer and hot melt extruders.
  • Additional work experience on parenteral and topical products is also beneficial
    Has developed products for ANDA/EU filing.
  • Has a basic understanding on the USFDA and EMEA guidelines for filing for drug products.
  • Responsible for execution of development trial batches and GMP batches under the supervision of senior scientists in the team.
  • Executes technical activities involving active pharmaceutical ingredients that may be potent or hazardous while following appropriate safety procedures.
  • Works independently supervised on a “weekly” basis, recognizes key issues likely to affect successful and/or timely completion.
  • For those issues that cannot be resolved by the project team, brings them to the attention of the line manager.
  • Completes development reports and regulatory support documentation as required.
  • Maintains an awareness of the current scientific practise and current good manufacturing processes
  • When requested, provides other support as required.
  • Complies with Health, Safety and Environmental responsibilities for the position.
  • Maintains current training records for required procedures.
  • Complies with departmental and company policies.
  • Follow environment, health, and safety (EHS) requirements at all times in the workplace ensuring individual and lab/plant safety
  • Attend training on environment, health, and safety (EHS) measures imparted company

Apply Online

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