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We bring to the prospective talents myriad award-winning career opportunities under disciplined working culture fostered to help you cultivate competence, excellence, and brilliance in your forte. Join us for rewarding career experience where talent is nurtured.

Regulatory Affairs

Qualification : BPharm / MPharm :
Experience : 12+ Years
Job Description :
  • Achieve timely submission of dossier deficiency responses to regulatory authority by reviewing, collating, and compiling documents in order to ensure approvals for launch in stipulated time.
  • Submit post approval variations for changes that improves productivity, cost-effectiveness, quality of the product by reviewing, collating, compiling the variation application to meet the delivery within timelines and maintain Product Marketing Authorization, Renewals to ensure continuous validity of marketing authorizations.
  • Maintain, and update product dossier as required to meet changes in internal systems, changes in regulatory guidelines, and to meet the need of regulatory requirements.
  • Update the database associated with product dossier approvals by including registration details in database.
  • Provide Regulatory support throughout the life cycle of the product for smooth functioning.
  • Check with regulatory authorities for submission activity and approval status for submission done.
  • Coordination with internal and external stakeholders for regulatory filing related documentation.
  • Review, compilation and authoring of as per regulatory requirements.
  • Review of plant and R&D documentation such as development reports, BMR, BPR, Specifications, method validation, process validation etc.
  • Consulting, categorizing, authoring Post approval changes through appropriate supplements.
  • Provide responses to regulatory agencies regarding product information or issues.
  • Train staff in regulatory policies or procedures.
  • Develop and maintain standard operating procedures or local working practices.
  • Establish regulatory priorities or budgets and allocate resources and workloads.
  • Communicate regulatory information to multiple departments and ensure that information is interpreted correctly.
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Quality Assurance

Position Title : Executive / Sr. Executive
Qualification : MPharm
Experience : 10+
Job Description :
  • Ensuring calibration and qualifications as per schedules.
  • To plan and co-ordinate for internal Audits.
  • Review of master formula records
  • Review the qualification / validation protocols, data and reports
  • Co ordinate and guide the IPQA Team.
  • Train the team members as per the standard operating procedures
  • Making sure that critical deviations are investigate.
  • Reviewing all specifications and master production instructions.
  • Reviewing all procedures impacting the quality of products.
  • Participate in the Periodic internal audits.
  • Reviewing the changes that potentially impact product quality.
  • Ensure quality related complaints are investigated.
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Information Technology

Position Title : Trainee /Jr.Executive
Qualification : Diploma / Any Degree
Experience : 0-2 Years
Job Description :
  • Local Network & Intercoms Maintainance.
  • Computer Issues.
  • Cable laying, Crimping, punching,
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Quality Control

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