Jubilant Biosys Hiring for DMPK roles in in vitro ADME & bioanalysis

Pharma Stuff; Dadri; On-site; INR 900,000 - 1,500,000; Full time

Benefits offered by this job

Publication opportunities

Cross-project exposure

Job summary

Jubilant Biosys Limited in Greater Noida seeks M.Pharm/PhD scientists for DMPK roles across levels from Associate to Group Lead. The team focuses on in vitro ADME, bioanalysis, and translational pharmacokinetics within a CRO environment that supports discovery-to-development programs.

Roles span Research Associate to Group Lead, offering exposure to method development, validation, and regulatory data packages, with LAB-based on-site work in Greater Noida.

Qualifications

• M.Pharm or PhD in Pharmaceutical Sciences or related discipline.
• Hands-on in vitro ADME and bioanalytical work; experience in PK data interpretation.

Responsibilities

• Design and execute in vitro ADME assays (metabolic stability, CYP, permeability, transporter assays).
• Develop, validate, and optimize LC-MS/MS bioanalytical methods for small molecules in biological matrices.
• Perform sample prep and operate LC-MS/MS/HPLC instruments; generate analytical data.
• Analyze PK/ADME data, prepare reports and scientific interpretation for decisions.
• Maintain GLP-compliant records, SOPs, and quality control for DMPK studies.
• Collaborate with discovery and project teams to support candidate progression.

Skills

In vitro ADME

Bioanalysis

PK/ADME data analysis

LC-MS/MS

CRO/pharma experience

Education

M.Pharm / PhD in Pharmaceutical Sciences

Tools

LC-MS/MS

HPLC

Method validation (ICH/GLP)

Job description

M.Pharm/PhD DMPK Roles at Jubilant Biosys, Greater Noida

Jubilant Biosys hiring M.Pharm/PhD for DMPK roles (2–15 yrs) in in vitro ADME & bioanalysis. Multiple levels: Associate to Group Lead, Greater Noida.

Jubilant Biosys is expanding its DMPK team in Greater Noida and looking for skilled scientists across experience levels — from Research Associate up to Group Lead. If you specialize in in vitro ADME, bioanalysis, or drug metabolism and want to work in a CRO environment that supports discovery-to-development programs, this is a high-visibility opportunity to contribute to translational pharmacokinetics and drug development projects.

Company Overview

Jubilant Biosys is a leading contract research organization offering integrated drug discovery and development services. The company supports global pharma and biotech partners with high-quality DMPK, bioanalytical, discovery, and translational research. Known for robust laboratory infrastructure, GLP-compliant workflows, and collaborative scientific teams, Jubilant delivers data-driven answers that accelerate candidate selection and regulatory submissions.

Job Role & Responsibilities

Jubilant is hiring for multiple positions within the DMPK team: Research Associate, Senior Research Associate, Research Scientist, Senior Research Scientist, Team Lead, and Group Lead. Roles vary by seniority but share core responsibilities centered on in vitro ADME, bioanalytical method development, and pharmacokinetic data generation.

Core Responsibilities (typical across levels)

• Design and execute in vitro ADME assays: metabolic stability (microsomes, hepatocytes), CYP inhibition/induction, enzyme phenotyping, plasma protein binding, permeability (PAMPA, Caco-2), transporter assays.
• Develop, optimize, and validate bioanalytical LC-MS/MS methods for quantifying small molecules in biological matrices.
• Perform sample preparation, extraction (SPE, protein precipitation), and instrument operation (LC-MS/MS, HPLC).
• Analyze PK and ADME data, generate reports, and provide scientific interpretation for decision-making.
• Maintain GLP-compliant records, SOP adherence, and quality control for DMPK studies.
• Collaborate with discovery, medicinal chemistry, toxicology, and project teams to support candidate progression.

Senior / Leadership Expectations

• Lead project workstreams, mentor junior scientists, and oversee assay transfer and troubleshooting.
• Guide method validation strategy, ensure data integrity, and support regulatory documentation packages.
• Drive process improvement, implement new assays or instrumentation, and shape team capability building.
• Coordinate CRO/vendor activities and maintain client-facing communications for project updates.

Minimum Education

• M.Pharm (Pharmaceutical Sciences) or PhD in Pharmaceutical Sciences, Pharmacology, Bioanalysis, or related discipline.

Experience Ranges

• Research Associate / Senior Research Associate: 2–6 years
• Research Scientist / Senior Research Scientist: 5–10 years
• Team Lead / Group Lead: 8–15 years (leadership and project management experience preferred)

Technical Skills & Knowledge

• Hands-on experience with in vitro ADME assays and bioanalytical LC-MS/MS workflows.
• Strong understanding of pharmacokinetics, drug metabolism, CYP/UGT pathways, and transporter biology.
• Experience with method development, validation (ICH/GLP expectations), and stability studies.
• Competency in data analysis tools and scientific reporting (PK parameters, noncompartmental analysis).
• Familiarity with quality systems and documentation practices in CRO/pharma settings.

Soft Skills

• Problem-solving and critical thinking with attention to experimental detail.
• Effective written and verbal communication for report writing and cross-functional interaction.
• Team leadership, mentoring, and stakeholder management for senior roles.

Location & Compensation

• Location: Greater Noida, Uttar Pradesh
• Work Model: On-site / lab-based
• Compensation: Competitive and aligned to experience level and technical expertise. Leadership roles include additional responsibility-based compensation and benefits.

Jubilant offers research-focused benefits, opportunities for publication, cross-project exposure, and a collaborative R&D culture.

Why this role matters

DMPK and bioanalytical data form the backbone of candidate selection and dosing strategy in drug development. By joining Jubilant’s DMPK team you will: contribute to translational pharmacology, support IND- and CTA-enabling studies, and influence go/no-go decisions for molecules advancing into clinical development.

FAQs

What backgrounds are suitable?

Candidates with M.Pharm or PhD in Pharmaceutical Sciences, Pharmacology, or Bioanalysis and hands-on ADME/bioanalysis experience are ideal.

Do I need CRO experience?

CRO experience is preferred but not mandatory for junior roles. Senior and leadership positions typically require CRO or pharma industry exposure.

Which instruments should I be familiar with?

LC-MS/MS, HPLC, autosamplers, centrifuges, and sample preparation systems are commonly used.

Are publication or validation records required?

They strengthen your application. Method validation experience and documented reports are highly valued.

What are growth opportunities?

Technical specialists can progress to senior scientist, team lead, and group lead roles; leadership roles may extend to program or site management.