Alembic Hiring Research Associate / Research Scientist – Technology Transfer
- Company Overview
- Job Role & Responsibilities
- Technology Transfer – Research Associate / Research Scientist
- Eligibility / Qualifications
- Location & Salary
- Application Process
- Why Build a Career in Technology Transfer?
- Frequently Asked Questions (FAQs)
- Summary
Meta Title: BPharm MPharm TT Jobs Vadodara | Alembic
Meta Description: B.Pharm, M.Pharm vacancies at Alembic Vadodara for Technology Transfer (2–5 yrs). Formulation manufacturing & regulatory support roles.
Alembic Pharmaceuticals is expanding its Technology Transfer (TT) function at its formulation manufacturing sites near Vadodara and is inviting experienced B.Pharm and M.Pharm professionals to join as Research Associate or Research Scientist. This opportunity is ideal for candidates with hands-on experience in product scale-up, process validation, regulatory documentation, and commercial batch execution within a regulated pharmaceutical environment.
If you are searching for Technology Transfer jobs in Vadodara, formulation development to manufacturing transition roles, pharma process validation careers, regulatory documentation B.Pharm jobs, or NPI (New Product Introduction) vacancies in Gujarat, this role offers structured exposure inside one of India’s leading pharmaceutical companies.
Company Overview
Alembic Pharmaceuticals is one of India’s established pharmaceutical manufacturers with a strong presence in domestic and regulated global markets. The company operates multiple formulation and API facilities that comply with international regulatory standards including USFDA and other global agencies.
The Technology Transfer (TT) team plays a critical role in bridging Product Development and Commercial Manufacturing. It ensures smooth scale-up from R&D to plant-level execution while maintaining compliance with cGMP, regulatory documentation standards, validation protocols, and data integrity practices.
Working within Alembic’s TT function provides high-value exposure to process risk assessment, regulatory filings, scale-up validation, and cross-functional coordination across Production, QA, QC, and Regulatory Affairs.
Job Role & Responsibilities
Technology Transfer – Research Associate / Research Scientist
Qualification: B.Pharm, M.Pharm
Experience: 2–5 years in Technology Transfer within formulation manufacturing
Location: Vadodara (Formulation Manufacturing Sites)
Key Responsibilities:
- Review Product Development Reports (PDR), Master Formula Cards (MFC), and Technology Transfer documentation.
- Provide technical inputs for process feasibility and commercial scale readiness.
- Prepare process risk assessments including identification of Critical Process Parameters (CPPs) and Critical Quality Attributes (CQAs).
- Draft and execute protocols for feasibility trials, scale-up batches, and exhibit batches.
- Prepare summary reports for trial and validation batches.
- Review and prepare Batch Manufacturing Records (BMR) and Batch Packaging Records (BPR).
- Support regulatory filings with commercial BMR, BPR, stability data, and evaluation summaries.
- Assist in regulatory documentation for Test License, Import License, NOC, and Manufacturing License.
- Contribute to Annual Product Review (APR) documentation.
- Support New Product Introduction (NPI) at manufacturing sites.
- Implement Process Analytical Technology (PAT) initiatives for process optimization.
- Prepare SOPs, technical justifications, and position papers.
The TT function is strategically positioned within the pharmaceutical value chain, ensuring that development-stage formulations successfully transition into robust, scalable commercial products compliant with regulatory expectations.
Eligibility / Qualifications
Required Educational Background:
B.Pharm, M.Pharm (Pharmaceutics, Industrial Pharmacy, Pharmaceutical Technology, Pharmaceutical Analysis, or related specialization).
Experience Requirement:
2–5 years of hands-on experience in Technology Transfer, scale-up, process validation, regulatory documentation, or formulation manufacturing in a regulated pharmaceutical plant.
Preferred Skill Set:
- Strong understanding of process validation and risk assessment tools.
- Experience in preparation and review of BMR, BPR, and TT documents.
- Familiarity with regulatory compliance requirements for global markets.
- Knowledge of QbD principles, CPPs, CQAs, and PAT systems.
- Strong technical documentation and cross-functional coordination skills.
Location & Salary
Work Location: Vadodara, Gujarat (Formulation Manufacturing Sites)
Salary: Competitive and aligned with industry standards based on experience and technical expertise.
Vadodara remains a major pharmaceutical hub offering long-term growth in formulation manufacturing, validation, and regulatory-focused roles.
Application Process
Interested candidates may share their updated profiles at:
msnt@alembic.co.in
Applicants should clearly mention “Technology Transfer – Research Associate/Scientist” in the subject line while applying.
Why Build a Career in Technology Transfer?
Technology Transfer roles offer strong long-term career growth because they combine formulation science, process engineering, regulatory documentation, and commercial manufacturing exposure. Professionals in TT gain visibility across multiple departments including R&D, Production, QA, QC, and Regulatory Affairs.
Experience in TT enhances career opportunities in:
- Process Validation Specialist roles
- Regulatory Affairs documentation
- Product Lifecycle Management
- New Product Introduction (NPI) leadership
- Pharmaceutical Project Management
Frequently Asked Questions (FAQs)
1. Is prior Technology Transfer experience mandatory?
Yes, 2–5 years of relevant TT or scale-up experience is preferred.
2. Which qualification is required?
B.Pharm or M.Pharm in relevant pharmaceutical specializations.
3. Is this role in R&D or Manufacturing?
It bridges both functions and focuses on transferring products from development to commercial manufacturing.
4. Does the role involve regulatory documentation?
Yes, including BMR/BPR preparation, stability documentation, and license support.
5. What skills are most important?
Process validation knowledge, risk assessment capability, and strong technical documentation skills.
Summary
| Company | Alembic Pharmaceuticals |
|---|---|
| Vacancies | Research Associate / Research Scientist – Technology Transfer |
| Required Education | B.Pharm, M.Pharm |
| Experience | 2–5 Years |
To apply for this job email your details to msnt@alembic.co.in