Lincoln Pharma Hiring B.Pharm/M.Pharm/M.Sc – R&D Roles

- Company Overview
- Job Role & Responsibilities
- 1. Method Development (2–10 Years)
- 2. Method Validation (2–10 Years)
- 3. Stability Study (1–6 Years)
- 4. GLP (2–8 Years)
- Eligibility / Qualifications
- Location & Salary
- Application Process
- Why Join Lincoln Pharmaceuticals?
- FAQs
- Job Summary Table
Lincoln Pharma Hiring B.Pharm/M.Pharm/M.Sc – R&D Roles
Lincoln Pharmaceuticals hiring for R&D roles in Method Development, Validation, Stability, and GLP. Apply now for Kalol, Gujarat openings.
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📱 Join Click HereLincoln Pharmaceuticals Ltd., one of India’s trusted pharma companies, is expanding its R&D hub at Kalol, Khatraj (Gujarat). As part of its Vision 2028 growth plan, Lincoln invites talented professionals to join its research and development team. This is a great opportunity to contribute to innovation in pharma and be part of an organization committed to global healthcare advancement.
Company Overview
Lincoln Pharmaceuticals Ltd. is a leading pharmaceutical company with a strong domestic and international presence. The company is known for its innovation-driven approach, robust R&D infrastructure, and focus on producing high-quality, affordable medicines. Lincoln’s R&D division is at the heart of its growth, focusing on method development, validation, stability studies, and GLP compliance to drive regulatory excellence and product quality.
Job Role & Responsibilities
Lincoln is hiring professionals for multiple R&D roles across Method Development, Method Validation, Stability Studies, and GLP compliance. Candidates with strong academic backgrounds and hands-on industry experience are encouraged to apply.
1. Method Development (2–10 Years)
- Operate instruments: HPLC, GC, UV, Dissolution apparatus
- Conduct method development and force degradation studies for FP & API
- Perform integration for assay and related substances
- Interpret pharmacopeia methods and perform literature searches
- Prepare method development protocols, trial data, and descriptive write-ups
For 5–10 years experience:
- Expertise in dissolution development and impurity profiling
- Review and interpretation of development trial data
- Preparation of detailed method protocols and reports
Subject Line for Application: MD
2. Method Validation (2–10 Years)
- Hands-on with HPLC, GC, UV, Dissolution apparatus
- Knowledge of regulatory guidelines: ICH, USP, WHO
- Integration for assay and related substances
- Preparation and review of method validation protocols and reports
- Data review and compliance-driven documentation
Subject Line for Application: MV
3. Stability Study (1–6 Years)
For 1–3 years:
- Perform stability sample analysis using HPLC/GC/UV/Dissolution apparatus
- Prepare stability testing worksheets
- Manage sample charging, withdrawal, and chamber operations
- Document stability trend records and summary reports
For 3–6 years:
- Plan, report, and review stability analyses
- Review testing protocols, worksheets, and chamber log records
- Coordinate review of OOS/OOT results with relevant teams
Subject Line for Application: ADL – Stability Study
4. GLP (2–8 Years)
- Ensure GLP compliance across laboratory activities
- Calibrate instruments as per schedules
- Manage chromatographic column issuance and performance checks
- Prepare, update, and revise SOPs
- Maintain records of reference standards, working standards, and impurities
- Ensure upkeep of all analytical instruments
Subject Line for Application: ADL – GLP
Eligibility / Qualifications
- Education: B.Pharm, M.Pharm, or M.Sc in relevant pharmaceutical/analytical fields
- Experience: 1–10 years depending on the role applied for
- Preferred Skills: Hands-on expertise with analytical instruments, compliance with ICH/USP/WHO guidelines, regulatory documentation, and GLP practices.
Relevant courses: Pharmaceutical Analysis, Analytical Chemistry, Biotechnology, Industrial Pharmacy, Quality Assurance, Pharmacology, Regulatory Sciences.
Location & Salary
- Location: Lincoln Pharmaceuticals R&D Center, Kalol, Khatraj (Gujarat)
- Salary: Competitive, based on qualifications and experience, with industry-standard benefits
Application Process
Interested candidates are requested to apply via email with the specified subject line for the role.
Email: sujitpillai@lincolnpharma.com
Mention subject line as: “Application for [Role] – Current Location: [City Name]”
Apply before 15th September 2025 to secure your spot.
Why Join Lincoln Pharmaceuticals?
- Opportunity to work in a state-of-the-art R&D facility
- Exposure to method development, validation, stability studies, and GLP
- Career growth with one of India’s most respected pharma companies
- Contribution to global healthcare through innovation
- Part of Lincoln’s Vision 2028 growth journey
FAQs
1. Who can apply for these roles?
Candidates with B.Pharm, M.Pharm, or M.Sc degrees and 1–10 years of relevant R&D experience.
2. What roles are open at Lincoln Pharmaceuticals?
Method Development, Method Validation, Stability Study, and GLP compliance.
3. Where is the job location?
Kalol, Khatraj (Gujarat).
4. What is the application process?
Send your CV to sujitpillai@lincolnpharma.com with the correct subject line.
5. What is the last date to apply?
Applications must be submitted by 15th September 2025.
Job Summary Table
Category | Details |
---|---|
Company | Lincoln Pharmaceuticals Ltd. |
Vacancies | Method Development, Method Validation, Stability Study, GLP (Multiple openings) |
Required Education | B.Pharm, M.Pharm, M.Sc |
Experience | 1–10 years depending on the role |
Location | Kalol, Khatraj, Gujarat |
To apply for this job email your details to sujitpillai@lincolnpharma.com