Research Scientist- Analytical R&D, PCC-PD&T

Piramal Pharma Limited; Navi Mumbai; On-site; INR 1,200,000 - 2,400,000; Full time

Job summary

Piramal Pharma Limited, Piramal Critical Care division, invites applications for Research Scientist- Analytical R&D in Rabale. You will perform analytical development, validation, and transfer for injectable and ophthalmic products, ensuring cGMP compliance and timely data generation.

Qualifications include M.Sc or M.Pharm and 5–8 years of pharma analytical experience, with hands-on work on HPLC, GC, UV and dissolution, plus readiness to collaborate with cross-functional teams and external

Qualifications

• Minimum 5–8 years of experience in Analytical R&D within the pharmaceutical industry.
• Hands-on experience in analytical method development, validation, method transfer, and stability studies.
• Exposure to injectable and/or ophthalmic products preferred.
• Experience in handling analytical instruments such as HPLC, GC, UV, dissolution, and related software.
• Exposure to regulatory documentation and cGMP practices.

Responsibilities

• Perform analytical method development, validation, verification, and transfer activities.
• Execute stability studies and routine analytical testing for development projects.
• Prepare analytical protocols, reports, specifications, STPs, and related documentation.
• Ensure compliance with cGMP, data integrity, and regulatory requirements.
• Maintain analytical instruments, laboratory records, and compliance readiness.

Skills

Analytical method development

Method validation

Method transfer

Stability studies

Regulatory documentation

Education

M.Sc /M. Pharm or equivalent

Tools

HPLC

GC

UV

Dissolution

Job description

Be the First to Apply Division Piramal Critical Care Piramal Critical Care (PCC), a business unit of Piramal Pharma, is the fourth-largest producer of inhaled anesthetics and a global player in hospital generics. We are motivated by our vision of commitment to delivering critical care solutions for patients and healthcare providers across the globe while achieving sustainable and profitable growth for all the stakeholders. PCC maintains a wide presence across the US, Europe, and more than 100 countries across the globe. Its rich product portfolio includes Inhalation Anesthetics such as Sevoflurane, Isoflurane and Halothane as well as Intrathecal Baclofen therapy, for spasticity management. PCC has a strong manufacturing and process development experience with wholly-owned, state-of-the-art manufacturing facilities in the United States and India, inspected periodically by the US FDA and the UK MHRA and other regulators. The strategic locations of our facilities help us supply high-quality products around the world, timely at optimal costs. For more details, please visit https://www.piramalcriticalcare.com/global/

Job Title

Research Scientist- Analytical R&D, PCC-PD&T

Job Description

To perform Analytical R&D activities for injectable and ophthalmic products across various stages of product development including analytical method development, validation, transfer, and stability studies. The role supports product development and regulatory activities by generating reliable analytical data in compliance with cGMP and regulatory requirements. The incumbent will work closely with cross-functional teams and external laboratories to ensure timely execution of analytical deliverables.

Business: Piramal Critical Care Department: PCC-PD&T Travel: Low Location: Rabale R&D Key Stakeholders Internal: Formulation, QA, SCM, RA, Program Management External: CMO, External testing Lab, Third party lab, Supplier

Essential Qualification

M.Sc /M. Pharm or equivalent

Relevant Experience

• Minimum 5–8 years of experience in Analytical R&D within the pharmaceutical industry.
• Hands-on experience in analytical method development, validation, method transfer, and stability studies.
• Exposure to injectable and/or ophthalmic products preferred.
• Experience in handling analytical instruments such as HPLC, GC, UV, dissolution, and related software.
• Exposure to regulatory documentation and cGMP practices.

Key Responsibilities

• Perform analytical method development, validation, verification, and transfer activities.
• Execute stability studies and routine analytical testing for development projects.
• Prepare analytical protocols, reports, specifications, STPs, and related documentation.
• Ensure compliance with cGMP, data integrity, and regulatory requirements.
• Maintain analytical instruments, laboratory records, and compliance readiness.

Key Competencies

• Strong knowledge of analytical techniques and pharmaceutical testing.
• Understanding of cGMP, ICH guidelines, and regulatory expectations.
• Effective communication and collaboration skills.
• Ability to manage multiple projects and timelines.
• Good documentation and technical writing skills.

Piramal Pharma Limited, offers a portfolio of differentiated products and services through its 17 global development and manufacturing facilities and a global distribution network in over 100 countries. PPL includes Piramal Pharma Solutions (PPS), an integrated Contract Development and Manufacturing Organization; Piramal Critical Care (PCC), a Complex Hospital Generics business; and the India Consumer Healthcare business, selling over-the- counter products. In addition, one of PPL’s associate companies, AbbVie Therapeutics India Private Limited is a JV with AbbVie Inc. and has emerged as one of the market leaders in the ophthalmology therapy area. Further, PPL has a minority investment in Yapan Bio Private Limited. In October 2020, PPL received a 20% strategic growth investment from the Carlyle Group.

PPL provides equal employment opportunities to all employees and applicants for employment. It prohibits discrimination and harassment based on race, color, age, sex, religion, national origin or ethnicity, disability status, genetics, protected veteran status, sexual orientation, gender identity, or expression, or any other characteristic protected by applicable law. Our employment decisions are based on merit considering qualifications, skills, performance, and achievements. Equal employment opportunity applies to all terms and conditions of employment, including recruitment, selection, training, social programs, placement, promotion, demotion, compensation and benefits, transfers, terminations, and working conditions.