Project Engineer - Katalyst Healthcares & Life Sciences
Cincinnati, OH 45201
About the Job
Responsibilities:
- We empower and support our colleagues.
- We commit to client success at every turn.
- We have the courage to do the right thing.
- We encourage an inclusive environment where our colleagues feel respected, engaged, and challenged.
- We constantly acquire new skills and learn from our experiences to enhance our collective expertise.
- Provide SME support to Manufacturing and other departments for the design and operation of process equipment, and facility (i.e. clean room) modifications
- Modify/develop preventative maintenance plans and create spare parts
- Effectively communicate progress and opportunities (i.e. roadblocks) to stakeholders.
- Manage project contractors
- Execute commissioning protocols
- Own change requests and complete change request tasks to support project completion
- Perform change request assessments
- Project Manager in the design and realization of the project until hand-over to operations in accordance with SOPs.
- Coordination of all technical disciplines involved including 3rd Parties
- Actively coordinates day to day activities with site resources to ensure no impact on al project activities.
- Project Manager to reach the project goals in terms of cost, time and functionality.
- Manage project progress, and escalation of issues.
- Coordination of Process Equipment specifications, URS, procurement, document control, receiving, installation and support CQV Manager.
- Support CQV Manager with Facility and equipment IOQ plan and process.
- Coordinate with stakeholders on day-to-day project execution requirements in regard to Operations, Facility Engineering and Quality.
- Must be willing to work mainly onsite in Cincinnati, OH.
- 1-3 Years relevant industry experience.
- Bachelor's Degree or equivalent required (Chemical Engineering or similar).
- Proficiency using PC and Microsoft Office tools.
- Outgoing personality with strong ability to communicate effectively with peers in clear, concise terms.
- Ability to work as part of a team.
- Strong problem-solving and critical thinking skills.
- Excellent organizational and time management skills.
- Strong attention to detail.
- GMP and Good Documentation Practice.
- Intermediate skills with WORD (authoring/editing large technical documents with styles, tables, TOCs, track changes).
- Basic skills with EXCEL and PowerPoint.
- Strong interpersonal skills and clear communication capabilities.
- Experience with and tolerance for high levels of challenge and change.
- Experience in GMP regulated environment.
- Proven attention to detail and organization in project work.
Source : Katalyst Healthcares & Life Sciences
