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Apply Online for Principal Scientist at Johnson & Johnson

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Johnson & Johnson, we believe health is everything. Our strength in healthcare innovation empowers us to build a world where complex diseases are prevented, treated, and cured, where treatments are smarter and less invasive, and solutions are personal. Through our expertise in Innovative Medicine and MedTech, we are uniquely positioned to innovate across the full spectrum of healthcare solutions today to deliver the breakthroughs of tomorrow, and profoundly impact health for humanity. 

Post : Principal Scientist, Synthetics Development AD

Summary : We are seeking a highly skilled analytical scientist with expertise in Mass Spectrometry (MS) applications to support pharmaceutical analytical method development and testing activities. The role will focus on supporting the development, optimization, validation, and troubleshooting of advanced analytical methods for Nitrosamines, Extractables & Leachables (E&L), and Elemental Impurities in compliance with global regulatory expectations.

Major Duties & Responsibilities :
Lead advanced analytical testing and investigation activities at the J&J IM R&D center in Mumbai and its associated CDMO’s in India through scientific contributions, oversight, shop floor presence whenever needed for troubleshooting etc…
• Scientific lead in following analytical areas :
o Mass Spectrometry expertise (to oversee Nitrosamine testing- method development and investigations, organic impurity identification and structural elucidation, Extractable & Leachable).
• Support development, optimization, validation and transfer of analytical methods using Mass Spectrometry techniques for pharmaceutical products and materials. 
• Knowledge and experience of working with Elemental impurities testing assessments via ICP MS (ICH Q3D, E&L), Particle Characterization and Morphology and NMR.
• Hands-on experience and expertise in handling analytical instruments like High Resolution and Low-Resolution Mass Spectroscopy (HRMS), LCMS/MS, GCMS/MS, ICP-MS, Laser Diffraction, Microscopy, NMR (Q_NMR)
• Interpret complex analytical data and prepare scientific protocols, reports, and regulatory documentation. 
• Participate in laboratory investigations, troubleshooting, root cause analysis, and continuous improvement initiatives.
• Collaborate with cross-functional teams including R&D, Quality Control, Regulatory Affairs, and external laboratories/vendors.
• Stay updated with emerging analytical technologies, regulatory trends, and industry best practices related to MS applications.
• Working experience in Oral Peptides and Antibody Drug Conjugates (ADC’s) is an added advantage.

Candidate Profile
Ph.D. in Analytical Chemistry, Pharmaceutical Sciences, Chemistry, or related scientific discipline
7-8 years of related experience

Required Knowledge, Skills and Abilities :
– In depth knowledge of API and DP development processes
– Regulatory guidelines and requirements in support of clinical studies and NDA/MAA filings
– Experience of working in cGMP environment
– Strong understanding of data interpretation, risk assessment, and analytical problem-solving. 
– Familiarity with global regulatory guidance related to Nitrosamines, E&L, and elemental 
impurities (ICH M7, USP <232>/<233>, USP <1663>/<1664>, etc.). 
– Excellent communication, technical writing, and collaboration skills.
– Exposure to packaging compatibility and toxicological risk assessment for E&L studies. 
– Knowledge of software tools for MS data acquisition and interpretation.
– Ability to work in a fast-paced, cross-functional pharmaceutical R&D environment.

Additional Information
Experience : 7-8 years
Qualification : Ph.D
Location : Mumbai 
Industry Type : Pharma/ Healthcare/ Clinical research
Functional Area : Synthetics Development AD
End Date : 31st July 2026

Principal Scientist : Apply Online

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