Sun Pharma Hiring Formulation R&D Scientist

Pharma Stuff; Vadodara; On-site; INR 1,000,000 - 1,400,000; Full time

Job summary

Sun Pharma’s Vadodara R&D team seeks a Formulation Research & Development Scientist (Non‑Orals) with 2–6 years of hands‑on experience in complex injectable or sterile formulations. You will contribute to regulated market development, scale‑up and tech transfer for sterile injectables.

You will design DoE/QbD studies, coordinate analytical method development, and prepare CMC‑ready documentation while collaborating with QA, QC, Production and Regulatory Affairs to ensure compliance and successful

Qualifications

• M.Pharm (Pharmaceutics) with 2–6 years in R&D for complex injectables or sterile formulations.
• Experience with lyophilization, aseptic processes, and high-potency APIs preferred.
• Strong skills in formulation design, DoE/QbD, pre‑formulation, stability planning and GMP documentation.

Responsibilities

• Lead formulation design and optimization for complex injectable products.
• Develop and execute pre‑formulation, excipient compatibility, forced‑degradation and stability studies.
• Design DoE/QbD experiments to optimize critical formulation and process parameters for scale‑up.
• Plan and execute pilot and exhibit batches; support technology transfer to the Vadodara manufacturing team.
• Prepare CMC‑ready documentation: development reports, method validation protocols, stability protocols and regulatory submissions.

Skills

Complex injectables

Lyophilization

Aseptic process design

HPLC/LC-MS

DoE/QbD

GMP documentation

Education

M.Pharm (Pharmaceutics)

B.Pharm

PG Diploma in Sterile Manufacturing

Certificate in Lyophilization

Certificate in QbD & DoE

PG Diploma in Regulatory Affairs

Tools

HPLC

LC-MS

DoE software

Job description

M.Pharm R&D (Complex Injections) – Vadodara

Sun Pharma hiring M.Pharm R&D professionals (2–6 yrs) for complex injectable formulation role in Vadodara.

Sun Pharma is recruiting experienced formulation scientists to join its Formulation Research & Development (Non‑Orals) team in Vadodara. This opening targets M.Pharm professionals with practical exposure to complex injectable dosage forms — biologics/sterile injectables, lyophilized products, or high‑potency parenterals — who can contribute to regulated market development, scale‑up and tech transfer activities.

Company Overview

Sun Pharmaceutical Industries Ltd. is a leading global pharmaceutical company known for a broad portfolio of branded and generic medicines. The company operates multiple R&D and manufacturing sites across India and internationally, and is recognised for strong compliance, robust quality systems, and investment in novel formulation technologies. Joining Sun Pharma’s Vadodara R&D team places you at a facility that supports sterile manufacturing, analytical development, and regulatory submissions for complex injectables intended for regulated markets.

Why this role matters

Complex injectable formulation scientists bridge lab development and commercial manufacturing. Your work ensures product safety, efficacy and manufacturability — directly impacting patient outcomes and regulatory approvals. The role offers exposure to high‑value skills such as aseptic processing, lyophilization strategy, formulation optimization, and regulatory dossier preparation for US/EU submissions.

Job Role & Responsibilities

As a Formulation Research & Development Scientist (Non‑Orals) you will:

• Lead formulation design and optimization for complex injectable products (sterile suspensions, solutions, lyophilized cakes, lyophilized reconstitution systems, high‑potency parenterals).
• Develop and execute pre‑formulation, excipient compatibility, forced‑degradation and stability indicating studies.
• Design DoE/QbD experiments to optimize critical formulation and process parameters for scale‑up.
• Plan and execute pilot and exhibit batches; support technology transfer to the Vadodara manufacturing team.
• Prepare CMC‑ready documentation: development reports, method validation protocols, stability protocols and regulatory submissions.
• Coordinate analytical method development and validation with QC/ADL teams (HPLC, LC‑MS, GC, dissolution where applicable).
• Work closely with QA, QC, Production and Regulatory Affairs to ensure batch release criteria, aseptic controls and data integrity.
• Troubleshoot formulation/process issues during scale‑up and commercial batches; lead investigations and CAPA implementation where necessary.
• Participate in cross‑functional project teams and mentor junior scientists.

Eligibility / Qualifications

• Required: M.Pharm (Pharmaceutics) with 2–6 years of hands‑on experience in pharmaceutical R&D focused on complex injectables or sterile formulations.
• Preferred: Experience with lyophilization, aseptic process design, terminal sterilization strategies, and handling of biologics or high‑potency APIs.
• Technical skills: formulation design, DoE/QbD, pre‑formulation, stability planning, analytical method familiarity (HPLC/LC‑MS), sterile tech transfer, and GMP documentation.
• Soft skills: clear technical writing, problem solving, cross‑functional collaboration, and project management.

Relevant courses (comma‑separated): M.Pharm Pharmaceutics, B.Pharm, PG Diploma in Sterile Manufacturing, Certificate in Lyophilization, Certificate in QbD & DoE, PG Diploma in Regulatory Affairs, M.Sc Pharmaceutical Sciences.

Location & Salary

• Location: Vadodara, Gujarat (on‑site role)
• Salary: Competitive and commensurate with experience; Sun Pharma offers structured benefits and performance incentives.
• Joining: Immediate to 30–45 days depending on notice period and availability.

FAQs

Q: Is hands‑on sterile manufacturing experience mandatory?
A: Yes — practical exposure to sterile/aseptic processes or injectable formulation development is essential.

Q: Can candidates with biologics experience apply?
A: Yes. Experience with biologics or peptide/protein formulations is valuable and transferable to complex injectables.

Q: Are remote or hybrid arrangements available?
A: No. This is an on‑site role at Vadodara due to laboratory and manufacturing coordination needs.

Q: What documents should I share?
A: CV, brief project summary highlighting injectable development or scale‑up experience, and relevant certificates.

Q: Does Sun Pharma support professional development?
A: Yes. The company invests in training, conferences, and internal knowledge programs for R&D staff.

Summary Table

• Company: Sun Pharmaceutical Industries Ltd.
• Vacancies: Formulation R&D Scientist – Non‑Orals (Complex Injectables)
• Required Education: M.Pharm (Pharmaceutics), B.Pharm, PG Diplomas in Sterile Manufacturing/Regulatory Affairs
• Experience: 2–6 years in pharmaceutical R&D with injectable/sterile formulation exposure

Tagged as: Analytical Research and Development