HomeHead/VP/CEO/President/GMR&D Head | Nitika Pharma | Nagpur

R&D Head | Nitika Pharma | Nagpur


NITIKA PHARMACEUTICAL SPECIALITIES PVT. LTD. ( NITIKA CHEMICALS ) was found in 1991 as a small manufacturing unit has grown today into a dynamic production center for a range of products finding applications in various Industry Verticals.

While achieving this growth we are still maintaining it as a family-owned enterprise to make the best of the advantages of being a closely held company.

Our focus is on the customer and achieving a high degree of customer satisfaction by providing quality products at a reasonable cost backed by timely deliveries and after-sales support.

Join Us for Regular Vacancy Updates on –

Join Our Telegram Group

Join Our Facebook Group

The company is a diverse group of people who work together to ensure the success of the company and contribute to making it a great place to work at.

We are looking for innovative employees in sectors like R&D, Quality Assurance, Quality Control, Production, Engineering, and Administration.

If you have innovative ideas that you want to share, we offer employees the opportunity to advance their personal skills and professional career. We are here to help you apply your talents and reach your goals.

Position: R&D Head

Location: Nagpur, Maharashtra, India

Job Description:

  • Propose, screen, evaluate and implement product and technology development projects
  • Lead in the development of new drug delivery technologies and products
  • Keep current with regulations and technical knowledge
  • Secure and provide adequate scientific formulation support to all assigned projects
  • Interface with internal and external clients in project meetings
  • Assist business development in preparation of R&D project proposals
  • Provide input on the technical feasibility and resources required of the project
  • Provide cost and man-hour estimates associated with R&D project proposals
  • Direct priorities within the position
  • Provide input on project planning
  • Comply with OSHA, EPA, DEA, and cGMP’s regulations
  • Maintain detailed records of all work to ensure compliance of all product submissions to the requirements of government agencies
  • Prepare and review CMC text for NDA/ANDA/DMF and other regulatory filings
  • Prepare and review master batch records, development pharmaceutics reports, and other formulation documents
  • Provide necessary training and mentoring to junior Formulation staff
  • Participate in the interview and hiring of qualified individuals to fill needed roles
  • Perform other tasks as requested by the Senior Director of Pharmaceutical Development

Qualification: M.Pharma

Experience: 7-12 Years

Salary: Negotiable

Contact Details:


If you are looking for a world-class company kindly revert with your updated CV along with CTC.ECTC and Notice Period

Click for More R&D Jobs

Click for More Top Pharma Jobs

Join Us for Regular Vacancy Updates on –

Join Our Telegram Group

Join Our Facebook Group


Please enter your comment!
Please enter your name here

- Advertisment -

Must Read