NPI & Tech Transfer Lead

MSD; Carlow; Hybrid; EUR 70,000 - 90,000; Full time

Job summary

MSD in Ireland is seeking a skilled NPI/Tech Transfer Specialist to support New Product Introductions and technical transfers. The role sits in the NPI Technical Engineering team, delivering process development, validation and equipment qualification for new products.

You will lead cross-functional efforts, perform data analysis, support Kaizen events and ensure compliance with cGMP and regulatory standards across Irish and European codes. Hybrid work arrangement is offered.

Qualifications

• Bachelor’s Degree or higher in science, engineering or technical discipline preferred.
• Minimum of three years within the pharmaceutical industry.
• Experience with GMP and regulatory standards applicable to Ireland/Europe/International.
• Knowledge of regulatory/code requirements to Irish, European and International Codes, Standards and Practices.
• Experience with equipment qualification and validation processes.

Responsibilities

• Support New Product Introductions and Technical Transfers.
• Provide process, technical, and validation support for manufacturing and new product introduction.
• Conduct analytical/engineering studies for new components, products, processes and facilities.
• Coordinate design and execution of equipment qualification and validation activities.
• Provide technical input into investigations and change controls; author/review/approve documentation.
• Lead or participate in Lean Six Sigma projects and continuous improvement initiatives.

Skills

Change Management

Equipment Qualification

GMP Compliance

Ishikawa Diagrams

Project Manufacturing

Sterile Processing

Technology Transfer

Education

Bachelor's Degree or higher

Job description

MSD in Ireland is seeking a skilled NPI/Tech Transfer Specialist to support New Product Introductions and technical transfers. The role sits in the NPI Technical Engineering team, delivering process development, validation and equipment qualification for new products.

You will lead cross-functional efforts, perform data analysis, support Kaizen events and ensure compliance with cGMP and regulatory standards across Irish and European codes. Hybrid work arrangement is offered.