Senior Research Associate – R&D
Location: Navi Mumbai, Maharashtra, India
Department: Research and Development
Business Unit: Piramal Pharma Limited (PPL)
Travel Requirement: Low
Job Overview
Piramal Pharma Limited (PPL) is seeking a skilled and motivated Senior Research Associate to join the Research & Development team. The role focuses on executing peptide synthesis and purification experiments, ensuring strict adherence to quality standards, regulatory requirements, and company policies. The ideal candidate will demonstrate operational discipline, strong analytical skills, and the ability to manage multiple priorities in a dynamic R&D environment.
Key Responsibilities
Adhere to Piramal core values, safety protocols, quality standards, and PSF guidelines.
Complete all assigned training programs in a timely manner.
Conduct planned experiments related to peptide synthesis and purification.
Document all experimental activities accurately and ensure timely updates in online systems.
Complete assigned projects and tasks within defined timelines.
Support team members as required and contribute to collaborative R&D efforts.
Monitor and analyze variations observed during process development of peptide synthesis and propose improvements.
Minimum Qualifications & Experience
Bachelor’s or Master’s degree in Chemistry, Pharmaceutical Sciences, or related field.
2–4 years of relevant experience in research and development, preferably in peptide synthesis, pharmaceutical process development, or API production.
Basic understanding of peptide synthesis principles is preferred.
Skills & Competencies
Strong attention to detail and commitment to quality.
Effective communication and interpersonal skills for teamwork and collaboration.
Ability to adapt to new processes, learn quickly, and manage multiple priorities efficiently.
Analytical mindset with problem-solving capabilities.
Proficiency in documentation practices and basic laboratory software/tools.
About Piramal Pharma Solutions (PPS)
Piramal Pharma Solutions (PPS) is a leading Contract Development and Manufacturing Organization (CDMO) providing end-to-end pharmaceutical development and manufacturing services globally. PPS operates through an integrated network across North America, Europe, and Asia, offering services including drug discovery, process and pharmaceutical development, clinical trial supplies, and commercial manufacturing of APIs and finished dosage forms. PPS specializes in advanced technologies including highly potent APIs, antibody-drug conjugates, sterile fill/finish, peptide products, and biologics including vaccines, gene therapies, and monoclonal antibodies. Our global expertise and trusted track record make PPS a preferred partner for innovators and generic companies worldwide.
Equal Employment Opportunity
Piramal Group is committed to equal employment opportunities and affirmative action. Employment decisions are based on merit, qualifications, skills, and performance without discrimination based on race, religion, gender, sexual orientation, disability, age, or other legally protected characteristics. Reasonable accommodations are provided for qualified individuals with disabilities and those with religious needs.
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