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Trainee - R&D

Piramal Pharma
Piramal Pharma
0-1 years
preferred by company
10 Jan. 22, 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

Trainee – Research & Development (R&D)

Location: Chennai, Tamil Nadu, India
Job Type: Full-Time
Experience Required: 0–1 Year
Industry: Pharmaceuticals / CDMO
Function: Research & Development – Synthesis Laboratory


Job Overview

Piramal Pharma Solutions is seeking a motivated Trainee – R&D to support synthesis laboratory operations and research activities. This entry-level role is ideal for candidates with an academic background in Chemistry or Organic Chemistry who are looking to build hands-on experience in pharmaceutical research and development while working in a cGMP- and GLP-compliant environment.


Key Responsibilities

  • Adhere strictly to cGMP, GLP, and internal safety guidelines at all times

  • Support day-to-day execution of chemical reactions under the guidance of senior scientists

  • Assist in interpreting analytical data to derive experimental conclusions

  • Support handling, operation, and routine maintenance of laboratory equipment

  • Ensure proper documentation of reactions and associated experimental data

  • Assist in calibration and upkeep of laboratory instruments

  • Contribute intellectually by sharing ideas related to reactions and ongoing projects

  • Collaborate effectively with cross-functional teams to support project execution

  • Participate in timely and successful completion of assigned R&D projects

  • Prepare weekly progress updates and final technical reports

  • Maintain accurate laboratory records in compliance with regulatory requirements


Required Qualifications

  • M.Sc. in Chemistry or Organic Chemistry

  • 0–1 year of hands-on experience in a synthesis or R&D laboratory (preferred)

  • Basic understanding of chemical synthesis and laboratory safety practices

  • Familiarity with cGMP and GLP guidelines is an advantage

  • Strong documentation, analytical, and problem-solving skills

  • Ability to work collaboratively in a team-based research environment

  • Willingness to learn and adapt in a fast-paced pharmaceutical R&D setting


About Piramal Pharma Solutions

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 globally integrated network across North America, Europe, and Asia, PPS delivers services spanning drug discovery, process development, clinical trial supplies, commercial API manufacturing, and finished dosage forms.

The organization also specializes in high-potency APIs, antibody-drug conjugates, sterile fill/finish, peptides, potent oral solids, and biologics, including vaccines, gene therapies, and monoclonal antibodies. Backed by decades of experience and advanced technologies, PPS is a trusted partner for global innovators and generic pharmaceutical companies.


Equal Employment Opportunity

Piramal Group is an Equal Employment Opportunity and Affirmative Action employer. Employment decisions are based solely on merit, qualifications, and business needs, without discrimination based on race, religion, gender, sexual orientation, age, disability, veteran status, or any other legally protected status. Reasonable accommodations are provided to qualified individuals as required by law.