What are the responsibilities and job description for the Technology Transfer Project Coordinator I position at bioMerieux SA?
Description
Technology Transfer Project Coordinator I
Position Summary
The Technology Transfer Project Coordinator I assist with projects of low complexity, manage assigned transfer-specific activities, and help communicate workflow and potential process changes to affected project teams. They support improvements to existing products and processes and assist in transferring of new products and processes to instrument manufacturing.
Primary Duties
- Perform all work in compliance with company policy and within bioMerieux's Quality System guidelines.
- Assist Technology Transfer Project Managers and coordinate updates, documentation releases, and cross-functional communication under the supervision from the Product Transfer Manager.
- Work with the Product Transfer Manager and/or Technology Transfer Project Manager to determine the scope of work and project timelines
- Schedule meetings, create agendas, and document meeting minutes, correspondence, and presentations.
- Coordinate and complete project and task transfer needs not already assigned to a Technology Transfer Project Manager with cross-functional teams.
- Report on the status of work packages to the Product Transfer Manager, Technology Transfer Project Manager, or Program Manager, as applicable.
- Performs other duties as assigned.
Supplemental Data
- This is an individual contributor role, not a supervisory role.
- No travel requirements.
- Ability to remain in stationary position, often standing, for prolonged periods.
Education, Training, Experience
-
Associates degree in a scientific or technical field
- In lieu of a degree, 4 years of directly related work experience in a technical or laboratory setting required.
- BS or BA in science or engineering preferred
Knowledge, Skills and Abilities
Required:
- Handle change and be flexible with tasks
- Able to accommodate changes in task prioritization
- Proficient in Microsoft Office program suite
- Strong documentation practices, organizational skills, and attention to detail
- Strong verbal and written communication skills
- Excellent interpersonal skills
- Ability to elicit cooperation from a wide variety of sources, including many departments within the company, and work as a team player
- Ability to problem-solve
Preferred:
- Ability to effectively prioritize and execute tasks in a fast-paced environment
- Ability to work both collaboratively and independently
- Strong decision-making skills
- Experience in cGMP, ISO 9001, and/or ISO 13485 compliance.
- Experience working in the medical device industry
- Experience working in a regulated environment
- Knowledge of Asana and Visio
