Research Scientist- Analytical RandD PCC-PDandT

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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.
  
  

• 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.
  
  

• 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.