Senior Research Scientist : Pharma Research OOD

Lupin

Pune District

On-site

INR 1,800,000 - 3,200,000

Full time

39 hours ago
Be an early applicant
Application generator

A complete application in a minute — tailored resume and cover letter, ready to send.

Get past ATS filters

Job summary

Lupin in Pune, MH, IN, seeks a Senior Research Scientist to drive formulation development for complex generics and Para IV ANDAs. The role involves pre-formulation, technology platforms, dissolution studies, and tech transfer for scale-up batches.

You will collaborate with QC/QA, Regulatory, and clinical teams, guiding a team of researchers to ensure high-quality outputs. Ideal candidates have M.Pharm or equivalent and 13+ years of experience, with a focus on drug delivery, innovation, and

Qualifications

  • Proven ability to lead drug formulation development projects.
  • Experience in scale-up and tech transfer.
  • Strong analytical and data interpretation skills.

Responsibilities

  • Develop novel controlled release and other dosage forms for complex generics and par IV/ANDA projects.
  • Lead cross-functional teams including QC/QA, Regulatory, and Marketing for product development.
  • Design, execute, and interpret dissolution tests and stability studies per ICH.
  • Prepare technical reports, CTD/CMC sections, and regulatory submissions.
  • Mentor and supervise research staff and ensure adherence to SOPs.

Skills

Research Leadership
Team Training
Process Improvement
Regulatory Knowledge
Project Management

Education

Masters in Pharmaceutical Technology

Job description

Senior Research Scientist : Pharma Research OOD
  • Date: Oct 6, 2026
  • Location: Pune_RD, MH, IN
  • Company: Lupin
    • Development of novel controlled release as well as non-infringing formulations (solid, liquid and injectable) for complex generics and first to file Para IV ANDAs for advanced (US, EU, Canada, Japan, Australia) and semi regulated markets with QBD approach. Carry out pre-formulation and formulation development experiments for new chemical entities and ANDA formulations. Develop new technology platforms and conduct feasibility studies for novel formulations such as microspheres, pellets, and spherules, aqueous and non-aqueous suspensions, ophthalmic and spray coated particles using various polymers. This includes preparation of prototype formulations for bio/clinical studies, analyzing experimental data and preparation of technical reports. Follow existing or prepare new SOPs and equipment operating procedures. Design, develop and conduct appropriate dissolution studies for the novel dosage forms. Prepare stability protocols and collect the stability data. As per ICH guidelines, set specifications for raw materials and finished products. Organize tech transfer of developed products to plants for the manufacturing of scale up, exhibit, clinical or bio study batches.
    • Review bio study and clinical study designs and protocols. Support clinical supply manufacturing and labeling activities along with drug supply inventory control and reconciliation. Maintain inventory and reconciliation of Innovator products. Ensure cost of development does not exceed its allocated cost.
    • Analyze and interpret significance of bio/clinical study results. Preparation and review of registration lot documents, technical reports and submission related documents in accordance with the applicable FDA and ICH guidelines such as CMC and CTD sections of IND, 505(b)2, NDA and Para III and IV certified ANDA. Maintain and follow safety standards as issued by the Company.
    • Lead interaction with QC, QA, Regulatory, Marketing, Clinical, Purchasing and Commercial departments for the successful development of new products.
    • Train and supervise Research associates/Trainees/Associate scientists.
    • Oversee continuous improvement initiatives, which includes analyzing the development capabilities and as necessary, redefining goals and objectives to improve quality and efficiency.
    • Take part in smooth functionality of department activities as per allotted KRA.
    Work Experience

    more than 13 years

    Education

    Masters in Pharmaceutical Technology

    Customer Centricity

    Developing Talent

    Process Excellence

    Result Orientation

    Stakeholder Management

    Strategic Agility

    1. Strategic Agility

    High Quality Standards

    Building a Safe Environment

    3. Customer Centricity

    5. Result Orientation

    6. Process Excellence

    Achievement Orientation

    Business Communication

    INNOVATION & CREATIVITY

    Connect With Us

    Follow our social channels to get a
    glimpse of life at Lupin

Get your free, confidential resume review.

or drag and drop your file here.

Similar jobs

Similar jobs worth comparing

Senior Research Scientist : Pharma Research OOD
Senior Research Scientist : Pharma Research OOD

Lupin • Maharashtra

On-site
INR 2,400,000 - 3,600,000
Senior Executive
Senior Executive

Lupin • Pithampur

On-site
INR 900,000 - 1,300,000
Manager - Business Development & Inlicensing
Manager - Business Development & Inlicensing

Lupin • Mumbai

On-site
INR 1,400,000 - 2,100,000
Sr Executive
Sr Executive

Lupin • Nagpur District

On-site
INR 1,800,000 - 2,600,000
Associate Scientist
Associate Scientist

Biopatrika • Pune District

On-site
INR 600,000 - 850,000
Lupin Hiring Packaging Development Executive
Lupin Hiring Packaging Development Executive

Pharma Stuff • Nagpur District

On-site
INR 600,000 - 1,200,000
Officer – Quality Assurance
Officer – Quality Assurance

Lupin • Pune District

On-site
INR 600,000 - 1,000,000
Manager- Technical Services (Formulation Development)
Manager- Technical Services (Formulation Development)

Pfizer • Goa

On-site
INR 3,000,000 - 6,000,000
Manager- Technical Services (Formulation Development)
Manager- Technical Services (Formulation Development)

Pfizer • Poriebhat

On-site
INR 3,000,000 - 6,000,000
Manager- Technical Services Formulation Development
Manager- Technical Services Formulation Development

Pfizer • Poriebhat

On-site
INR 3,000,000 - 6,000,000