Executive / Sr Executive -Technology Transfer

MSN Group; Hyderabad; On-site; INR 900,000 - 1,300,000; Full time

Job summary

MSN Laboratories in Hyderabad, Telangana seeks an Executive / Senior Executive to support formulation technology transfer from R&D to manufacturing. You will coordinate cross-functionally, review development data, and drive scale-up with process validation readiness.

The role requires 2–6 years of relevant experience and strong documentation skills. Exposure to GMP, regulatory requirements, and continued process verification will be important as you contribute to successful commercialization of

Qualifications

• Experience in formulation development and manufacturing processes.
• Exposure to scale-up, tech transfer, and regulated pharma operations.
• Strong documentation and regulatory compliance experience.

Responsibilities

• Execute technology transfer from R&D to commercial manufacturing for OSDs.
• Review development reports, MBRs, process parameters, specs, and analytics.
• Prepare tech transfer docs: protocols, reports, process descriptions, risk assessments.
• Coordinate with cross-functional teams including QA, QC, Regulatory, and Engineering.
• Support scale-up activities, validation, and continued process verification.
• Monitor CPPs/CQAs during scale-up and tech transfer, identify CAPA.
• Investigate deviations/OOS/OOT and assist root-cause analysis.
• Ensure GMP, SOPs, and regulatory compliance across sites.
• Maintain documentation and support regulatory filing activities.

Skills

Formulation R&D

Scale-up

Technology transfer

Documentation

Education

M.Pharm / M.S. / B.Pharm in Pharmaceutics or related

Job description

Role & responsibilities

Company: MSN Laboratories
Department: Formulation Technology Transfer
Designation: Executive / Senior Executive
Experience: 2–6 Years
Location: Hyderabad, Telangana

Job Purpose

To support and execute formulation technology transfer activities from R&D/Development to manufacturing sites, ensuring smooth scale-up, process validation readiness, regulatory compliance, and successful commercialization of pharmaceutical products.

Key Responsibilities

• Execute technology transfer activities for oral solid dosage formulations from R&D/Development to commercial manufacturing.
• Review and understand formulation development reports, batch manufacturing records, process parameters, specifications, and analytical requirements.
• Prepare and review technology transfer documents, including technology transfer protocols, reports, process descriptions, and risk assessments.
• Coordinate with Formulation R&D, Production, Quality Assurance, Quality Control, Engineering, Regulatory Affairs, and other cross-functional teams.
• Participate in scale-up, exhibit, engineering, validation, and commercial batches.
• Monitor critical process parameters (CPPs) and critical quality attributes (CQAs) during scale-up and technology transfer activities.
• Support troubleshooting of manufacturing/process-related issues and assist in identifying root causes and appropriate CAPA.
• Review manufacturing and development data to identify process gaps and opportunities for improvement.
• Ensure compliance with GMP, SOPs, regulatory requirements, and internal quality systems.
• Support preparation and execution of process validation and continued process verification activities.
• Assist in investigation of deviations, OOS/OOT results, and process-related discrepancies.
• Prepare technical reports, presentations, and other documentation required for technology transfer and commercialization.
• Coordinate with manufacturing sites for successful implementation of transferred products.
• Support regulatory filing requirements by providing technical and process-related information.
• Maintain proper documentation and ensure timely closure of technology-transfer activities.

Desired Technical Knowledge

• Pharmaceutical formulation development and manufacturing.
• Oral solid dosage forms such as tablets and capsules.
• Scale-up and technology transfer principles.
• Granulation, blending, compression, coating, encapsulation, and related manufacturing processes.
• Critical Process Parameters (CPPs) and Critical Quality Attributes (CQAs).
• QbD, Quality Risk Management, and process validation concepts.
• GMP, GDP, and pharmaceutical documentation practices.
• Deviation, change control, CAPA, and investigation processes.

Education

Required: M.Pharm / M.S. / B.Pharm in Pharmaceutics, Pharmaceutical Technology, or a related discipline.

Experience

• Executive: 2–4 years of relevant experience in Formulation R&D, Scale-up, Technology Transfer, or Pharmaceutical Manufacturing.
• Senior Executive: 4–6 years of relevant experience in Formulation Technology Transfer / Scale-up / Manufacturing.
• Experience in regulated pharmaceutical manufacturing and handling technology-transfer projects is preferred.

Key Competencies

• Strong technical understanding of formulation and manufacturing processes.
• Good analytical and problem-solving skills.
• Cross-functional coordination and communication.
• Strong documentation and report-writing skills.

Knowledge of GMP and regulatory expectations.

Ability to work effectively with R&D, Production, QA, QC, and other stakeholders.

Willingness to travel between development and manufacturing sites when required.