Jubilant Biosys Hiring for DMPK roles in in vitro ADME & bioanalysis
- M.Pharm/PhD DMPK Roles at Jubilant Biosys, Greater Noida
- Company Overview
- Job Role & Responsibilities
- Core Responsibilities (typical across levels)
- Senior / Leadership Expectations
- Eligibility / Qualifications
- Minimum Education
- Experience Ranges
- Technical Skills & Knowledge
- Soft Skills
- Location & Compensation
- How to Apply
- Why this role matters
- FAQs
- What backgrounds are suitable?
- Do I need CRO experience?
- Which instruments should I be familiar with?
- Are publication or validation records required?
- What are growth opportunities?
- Summary Table
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.
Eligibility / Qualifications
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.
How to Apply
Email your CV and a concise cover note highlighting relevant DMPK and bioanalytical experience to: seema.bhatt@jubilantbiosys.com
In your email, specify the preferred role (e.g., Research Scientist — DMPK) and clearly list your hands-on experience with ADME assays, LC-MS/MS, and any leadership responsibilities. Candidates with publications, method validation records, or client-facing experience should include those highlights.
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.
Summary Table
| Category | Details |
|---|---|
| Company | Jubilant Biosys, Greater Noida |
| Vacancies | Research Associate, Senior Research Associate, Research Scientist, Senior Research Scientist, Team Lead, Group Lead (DMPK) |
| Required Education | M.Pharm, PhD (Pharmaceutical Sciences, Pharmacology, Bioanalysis) |
| Experience | 2–15 years (role-dependent; CRO experience preferred) |
To apply for this job email your details to seema.bhatt@jubilantbiosys.com
