About the Role
The Project Manager will be responsible for safely coordinating and leading projects associated with new product introductions, process improvements, automation, aseptic processing, and facility modifications.
This is an excellent opportunity to join our team as a Project Manager and take on a challenging role that requires strong project management skills, technical knowledge, and leadership abilities.
Key Responsibilities
* Safely coordinate and lead cross-functional project teams for the delivery of processing equipment to the site based on planned timelines and scope.
* Write User Requirement Specifications.
* Select vendors and complete vendor evaluation matrices.
* Write Requests for Change (RCEs), place orders, and attend project management and design review meetings.
* Work to the ASME BPE 2019 Standard and relevant ISPE guidelines.
* Coordinate processing equipment installation and services hook-up, working with equipment vendors and engineering personnel.
* Lead the project team's participation in Factory Acceptance Testing programs.
* Coordinate all equipment documentation requirements.
* Commission equipment and provide engineering support during qualification.
Requirements
* Educational background: third-level qualification in an engineering or equivalent discipline/experience.
* Experience of working in the biologics, pharmaceuticals, or medical device industry.
* Minimum of 2-5 years' experience.
* Project management experience with a proven record.
* A self-starter with proven technical ability.
Additional Information
This role involves travel for design review meetings, build inspections, and Factory Acceptance Tests.