Tech Transfer Lead
PharmEng Technology
Dato: for 2 uger siden
By: Hillerød, Region Hovedstaden
Kontrakttype: Entreprenør

About The Job Tech Transfer Lead
Permanent
Position: Tech Transfer Lead
Company Overview
Efor Group is a leading pharmaceutical consulting firm that provides a full range of services to the global pharmaceutical, biotechnology, and medical device industries. Our team of experts delivers innovative solutions that help our clients bring their products to market faster and more efficiently.
Location:
This position is based at a client site in Hillerød, Denmark.
Contract Details
This is a full-time, permanent position with competitive salary and benefits package.
Job Description
We are seeking a highly motivated and experienced Tech Transfer Lead to join our growing team in Copenhagen. The Tech Transfer Lead will be responsible for leading and managing all aspects of technology transfer projects for our clients, from development to commercialization.
Key Responsibilities
Permanent
Position: Tech Transfer Lead
Company Overview
Efor Group is a leading pharmaceutical consulting firm that provides a full range of services to the global pharmaceutical, biotechnology, and medical device industries. Our team of experts delivers innovative solutions that help our clients bring their products to market faster and more efficiently.
Location:
This position is based at a client site in Hillerød, Denmark.
Contract Details
This is a full-time, permanent position with competitive salary and benefits package.
Job Description
We are seeking a highly motivated and experienced Tech Transfer Lead to join our growing team in Copenhagen. The Tech Transfer Lead will be responsible for leading and managing all aspects of technology transfer projects for our clients, from development to commercialization.
Key Responsibilities
- Ensure information/communication to WPO regarding project changes, updates, customer comments etc.
- Request resources for TT Team, schedules and leads TT meetings (incl. agenda/minutes and action follow-up)
- Create overall Validation Strategy
- Create and maintain TT Project Plan
- Internal kick off
- Own and maintain document tracker
- One point of contact with customer
- Own and update the overall TT Board
- Status reporting escalation to management
- Create overall program CMR
- Create TTP, if applicable
- Owner overall TT meeting (WPOs and other stakeholders, QA ops, QRM etc.)
- Create collaboration tools:
- TEAMS site build
- TEAM site access
- Minutes templates
- Templates in general
- Bachelor's or Master's degree in engineering, pharmaceutical sciences, or a related field.
- Minimum of 5 years of experience in technology transfer, process development, or manufacturing in the pharmaceutical industry.
- Strong project management skills, with a track record of successfully leading and managing complex projects.
- Excellent communication and interpersonal skills.
- Experience with regulatory requirements and industry standards for pharmaceutical products.
- Ability to work independently and in a team environment.
- Fluent in English, both written and spoken.
- Willingness to travel as needed.
- Competitive salary and benefits package.
- Opportunities for professional growth and development.
- A dynamic and collaborative work environment.
- The chance to be part of a growing and innovative company that is making a difference in the pharmaceutical industry.
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