Alembic Hiring Research Associate Technology Transfer

M.Pharm 1–5 Yr Research Associate TT | Vadodara

M.Pharm candidates – Research Associate Technology Transfer vacancy at Alembic Pharma formulation site in Vadodara. 1–5 yrs experience required.

Alembic Pharmaceuticals is hiring a Research Associate for its Technology Transfer (TT) function at its formulation manufacturing operations. This role focuses on oral solid dosage (OSD) technology transfer activities that bridge pharmaceutical product development and commercial manufacturing. Candidates with an M.Pharm qualification and experience in pharmaceutical technology transfer, formulation scale‑up, or manufacturing science and technology (MS&T) environments are encouraged to apply.

Technology transfer professionals play a critical role in ensuring that drug formulations developed during R&D are successfully scaled to commercial manufacturing. This involves translating laboratory‑scale pharmaceutical formulations into robust, reproducible, and regulatory‑compliant manufacturing processes.

The position provides an opportunity to work in a highly regulated pharmaceutical environment where professionals collaborate with formulation development teams, manufacturing units, regulatory affairs specialists, and quality assurance teams. Candidates joining this role will gain exposure to scale‑up manufacturing, process validation, regulatory documentation, and new product introduction (NPI) for global pharmaceutical markets.

For professionals seeking careers in pharmaceutical process development, manufacturing science, regulatory compliance, and technology transfer, this position offers strong long‑term growth within a globally recognized pharmaceutical organization.

Company Overview

Alembic Pharmaceuticals Ltd. is one of India’s oldest and most respected pharmaceutical companies with more than 100 years of excellence in healthcare innovation. Founded in 1907, the company has built a strong global presence in pharmaceutical manufacturing, formulation development, and active pharmaceutical ingredient (API) production.

Alembic operates multiple state‑of‑the‑art manufacturing facilities that comply with international regulatory standards including US FDA, WHO‑GMP, and EU regulatory guidelines. The company exports pharmaceutical products to numerous international markets and maintains a robust research and development pipeline focused on high‑quality generic medicines.

The organization is widely recognized for its contributions to cardiovascular, anti‑infective, anti‑diabetic, and other therapeutic segments. With a strong focus on pharmaceutical research, quality compliance, and advanced manufacturing technology, Alembic continues to expand its presence in regulated global markets.

The formulation sites operated by Alembic are equipped with advanced pharmaceutical manufacturing infrastructure designed for oral solid dosage forms such as tablets and capsules. These facilities follow strict Good Manufacturing Practice (GMP) standards and operate under global regulatory oversight.

Technology transfer teams within Alembic play a central role in translating pharmaceutical R&D innovations into scalable commercial production processes that ensure consistent product quality and patient safety.

Job Role & Responsibilities

The Research Associate – Technology Transfer role supports the transfer of pharmaceutical formulations from development laboratories to commercial manufacturing facilities. The position requires collaboration with multiple cross‑functional teams including R&D, manufacturing, quality assurance, and regulatory affairs.

Technology Transfer – Oral Solid Dosage (OSD)

Technology transfer professionals ensure that pharmaceutical formulations are successfully scaled from development stage to commercial manufacturing while maintaining product quality and regulatory compliance.

Key responsibilities include:

• Reviewing Product Development Reports (PDR) and Master Formula Cards (MFC)
• Providing technical inputs during preparation and review of Technology Transfer (TT) documentation
• Preparing risk assessment documentation for pharmaceutical manufacturing processes
• Designing and executing feasibility trials and scale‑up batches
• Preparing protocols and reports for manufacturing trials
• Executing exhibit batches and preparing technical reports
• Preparing and reviewing Batch Manufacturing Records (BMR)
• Reviewing Batch Packaging Records (BPR) for regulatory compliance

Process Development & Scale‑Up

A major responsibility of the role is supporting scale‑up activities that convert laboratory‑scale formulations into commercially viable manufacturing processes.

Key responsibilities include:

• Conducting trial batches for process optimization
• Monitoring scale‑up manufacturing batches
• Evaluating manufacturing performance and process consistency
• Preparing technical summaries of manufacturing trials
• Supporting process validation and process robustness initiatives

Regulatory Documentation Support

Technology transfer teams support regulatory filings by preparing manufacturing documentation required for drug approvals and regulatory submissions.

Key responsibilities include:

• Preparing intended commercial Batch Manufacturing Records (BMR)
• Supporting preparation of Batch Packaging Records (BPR)
• Preparing stability execution and evaluation summaries
• Supporting regulatory documentation for product submissions
• Ensuring compliance with global pharmaceutical regulatory requirements

Licensing & Regulatory Compliance

The role also involves supporting regulatory approvals related to pharmaceutical manufacturing and product commercialization.

Key responsibilities include:

• Supporting documentation for Test License approvals
• Assisting with Import License documentation
• Preparing documents for No Objection Certificates (NOC)
• Supporting Manufacturing License applications
• Providing product and process documentation required by regulatory agencies

Process Optimization & Quality Improvement

Technology transfer teams contribute to continuous improvement of pharmaceutical manufacturing processes.

Key responsibilities include:

• Reviewing Critical Process Parameters (CPPs)
• Evaluating Critical Quality Attributes (CQAs)
• Supporting Annual Product Review (APR) activities
• Implementing Process Analytical Technology (PAT) initiatives
• Identifying opportunities for process optimization

New Product Introduction (NPI)

Research associates also support the introduction of new pharmaceutical products at manufacturing facilities.

Responsibilities include:

• Supporting NPI activities at formulation manufacturing sites
• Coordinating with R&D and production teams during product launch
• Ensuring smooth transfer of manufacturing processes
• Supporting documentation required for product commercialization

Documentation & SOP Development

Documentation accuracy is critical in pharmaceutical manufacturing environments.

Responsibilities include:

• Preparing Standard Operating Procedures (SOPs)
• Maintaining GMP compliant documentation
• Reviewing manufacturing and quality documentation
• Ensuring adherence to regulatory documentation standards

Eligibility / Qualifications

Candidates applying for this role must have a postgraduate degree in pharmaceutical sciences with experience in technology transfer, pharmaceutical process development, or manufacturing science and technology.

Required Educational Background

M.Pharm Pharmaceutics, M.Pharm Pharmaceutical Technology, M.Pharm Industrial Pharmacy, M.Pharm Drug Regulatory Affairs, M.Pharm Quality Assurance, M.Pharm Pharmaceutical Analysis

Candidates with strong knowledge of pharmaceutical formulation development, scale‑up processes, and manufacturing documentation will be preferred.

Experience Requirement

1 to 5 years of relevant experience in:

• Pharmaceutical technology transfer
• Oral solid dosage (OSD) manufacturing
• Manufacturing Science & Technology (MS&T)
• Pharmaceutical formulation scale‑up
• Pharmaceutical regulatory documentation

Experience working in USFDA or other regulated pharmaceutical environments will be an advantage.

Preferred Candidate Skills

The ideal candidate should demonstrate:

• Strong understanding of pharmaceutical formulation processes
• Knowledge of GMP and regulatory compliance
• Experience in scale‑up and process validation
• Familiarity with pharmaceutical manufacturing documentation
• Strong technical writing and documentation skills
• Ability to collaborate with cross‑functional teams

Location & Salary

Job Location

Alembic Pharmaceutical Formulation Site

Vadodara
Gujarat, India

Vadodara is one of India’s major pharmaceutical manufacturing and research hubs. Many global pharmaceutical companies operate manufacturing plants and R&D centers in this region.

Working at Alembic’s formulation facility offers exposure to large‑scale pharmaceutical production, global regulatory standards, and advanced manufacturing technologies.

Salary

Compensation for research associate roles in technology transfer depends on experience, pharmaceutical industry exposure, and technical expertise. Candidates with experience in formulation scale‑up, regulatory documentation, and manufacturing science typically receive competitive pharmaceutical industry salary packages.

Additional benefits may include professional training programs, exposure to global regulatory systems, and long‑term career growth opportunities within pharmaceutical R&D and manufacturing functions.

Application Process

Interested candidates can submit their updated profile directly to the company’s recruitment team.

Send your CV to:

msnt@alembic.co.in

Candidates should mention the subject line:

“MS&T”

Applicants are advised to include detailed information in their resume such as:

• Academic qualifications
• Pharmaceutical industry experience
• Technology transfer or scale‑up project experience
• Process validation or manufacturing documentation experience
• Contact information

Shortlisted candidates may be contacted for technical interviews and further evaluation.

Why Build a Career in Pharmaceutical Technology Transfer

Technology transfer is one of the most critical functions in pharmaceutical manufacturing because it ensures that drug formulations developed during research are successfully converted into scalable and compliant commercial manufacturing processes.

Professionals working in technology transfer gain expertise in formulation development, manufacturing science, regulatory compliance, and pharmaceutical process engineering. These skills are highly valuable across the global pharmaceutical industry.

Typical career progression includes roles such as:

• Technology Transfer Scientist
• Manufacturing Science & Technology (MS&T) Specialist
• Pharmaceutical Process Development Scientist
• Validation Specialist
• Pharmaceutical Production Scientist
• Technical Services Manager

As pharmaceutical companies continue to launch new drug products globally, demand for professionals skilled in formulation scale‑up and manufacturing technology transfer continues to grow.

Frequently Asked Questions (FAQs)

What qualification is required for the Alembic Research Associate role?

Candidates must hold an M.Pharm degree in pharmaceutics, pharmaceutical technology, industrial pharmacy, or related pharmaceutical disciplines.

What experience is required for this position?

The company is looking for candidates with 1–5 years of experience in technology transfer, formulation scale‑up, or pharmaceutical manufacturing science.

What does a technology transfer professional do?

Technology transfer specialists ensure that pharmaceutical formulations developed in R&D are successfully scaled to commercial manufacturing while maintaining quality and regulatory compliance.

Where is the job located?

The role is based at Alembic’s formulation manufacturing site in Vadodara, Gujarat.

How can candidates apply?

Candidates can submit their CV directly to the recruitment email provided by the company with the subject line “MS&T”.

Job Summary

Company	Alembic Pharmaceuticals Ltd.
Vacancies	Research Associate – Technology Transfer (OSD), MS&T Research Associate
Required Education	MPharm Pharmaceutics, MPharm Pharmaceutical Technology, MPharm Industrial Pharmacy, MPharm Drug Regulatory Affairs, MPharm Quality Assurance
Experience	1–5 Years