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Senior Principal Scientist - Synthesis

Piramal Pharma
Piramal Pharma
10+ years
preferred by company
10 Jan. 30, 2026
Job Description
Job Type: Full Time Education: B.Sc./ M.Sc./ M.Pharm/ B.Pharm/ Life Sciences Skills: Causality Assessment, Clinical SAS Programming, Communication Skills, CPC Certified, GCP guidelines, ICD-10 CM Codes, CPT-Codes, HCPCS Codes, ICD-10 CM, CPT, HCPCS Coding, ICH guidelines, ICSR Case Processing, Interpersonal Skill, Labelling Assessment, MedDRA Coding, Medical Billing, Medical Coding, Medical Terminology, Narrative Writing, Research & Development, Technical Skill, Triage of ICSRs, WHO DD Coding

Senior Principal Scientist – Peptide Synthesis | Navi Mumbai, Maharashtra, India | Full-Time

Location: Navi Mumbai, Maharashtra, India
Experience Required: Minimum 10+ years in peptide synthesis and purification
Industry: Pharmaceutical R&D / Peptide Chemistry / Drug Development
Employment Type: Full-Time


About Piramal Pharma Solutions (PPS)

Piramal Pharma Solutions (PPS) is a leading Contract Development and Manufacturing Organization (CDMO) providing end-to-end solutions across the drug development lifecycle. With a global network spanning North America, Europe, and Asia, we deliver comprehensive services including drug discovery, process and pharmaceutical development, clinical trial supply, commercial API and dosage form manufacturing, and specialized services such as peptides, highly potent APIs, antibody-drug conjugates, sterile fill/finish, and biologics.

For over three decades, Piramal Group has driven growth through innovation, ethics, and values-driven practices, making it a trusted partner for global innovators and generic companies.


Role Overview

The Senior Principal Scientist – Peptide Synthesis will provide technical and strategic leadership in peptide research and development. This role is responsible for driving innovation, optimizing synthesis and purification processes, and guiding multidisciplinary teams to achieve scientific and operational excellence.

You will play a critical role in advancing the peptide R&D program, ensuring compliance with regulatory requirements, and supporting organizational goals in alignment with PPS’s vision for innovation in pharmaceutical development.


Key Responsibilities

Research & Development Leadership:

  • Develop and implement strategic plans for peptide synthesis in line with organizational objectives.

  • Lead peptide synthesis projects from concept to completion, ensuring quality, timelines, and budgets are achieved.

  • Collaborate with process development and purification teams to integrate peptide synthesis into downstream processes efficiently.

  • Drive innovation by exploring new techniques, technologies, and chemical methodologies.

Team & Knowledge Development:

  • Train, mentor, and guide research teams in advanced chemical technologies and peptide synthesis methods.

  • Foster a culture of innovation, safety, and scientific excellence within the R&D team.

  • Support major EHS initiatives and drive continuous improvement in laboratory practices.

Operational Excellence & Compliance:

  • Take ownership of process optimization, solvent recovery, and yield improvement.

  • Ensure compliance with regulatory guidelines governing peptide drug development.

  • Assist teams in successful regulatory inspections with minimal observations.

  • Manage stakeholder interactions with internal teams, vendors, and customers as needed.


Required Experience & Skills

  • Experience: Minimum 10+ years in peptide synthesis and purification, with proven leadership in R&D projects.

  • Technical Skills: Expertise in peptide synthesis, purification, and process optimization. Strong analytical and problem-solving abilities.

  • Leadership Skills: Ability to lead multidisciplinary teams, make data-driven decisions, and manage stakeholder expectations.

  • Soft Skills: Excellent communication, decision-making, risk assessment, and strategic planning capabilities.

  • Education: M.Sc. or PhD in Chemistry, Biochemistry, Pharmaceutical Chemistry, or related disciplines.


Why Join Piramal Pharma Solutions

  • Work with a globally recognized CDMO with a strong presence in North America, Europe, and Asia.

  • Lead cutting-edge peptide research and contribute to innovative drug development.

  • Collaborate with world-class teams in a dynamic, inclusive, and values-driven environment.

  • Benefit from a comprehensive equal opportunity culture promoting career growth, development, and ethical practices.

Piramal Group is proud to be an Equal Employment Opportunity employer, committed to diversity, equity, and inclusion. All qualified applicants will receive consideration regardless of race, ethnicity, gender, religion, age, disability, or other legally protected characteristics.

Apply now to lead peptide synthesis innovation and drive scientific excellence at Piramal Pharma Solutions, Navi Mumbai.