Job Title: Project Manager, Engineering
Location: Meriden, CT
Duration: 12 Months+
Pay: $65/hr. on W2
Work Schedule: Monday – Friday Days
Description: Role Summary
Environmental Conditions:

• Office environment with extended periods in seated position
• Manufacturing environment including some areas with elevated noise levels
• Manufacturing environment including controlled and uncontrolled cleanroom areas
• PPE (safety glasses, gowning, gloves, lab coat, ear plugs etc.) as required by area
• Adherence to all GMP (Good Manufacturing Practices) and safety standards required.

Role impact

• This role is part of the capital engineering team to manage facilities projects that support *** FSD (Filtration and Separation Division) manufacturing sites.
• It will be responsible for ensuring the quality, safety, and performance in the execution of manufacturing facilities projects including feasibility, specification, design, and build.
• This role will have direct responsibility for facilities projects to improve utilization, productivity, capacity, cost reduction, and efficiency of existing facilities. It will be responsible for ensuring the highest levels of workmanship and professionalism.

Role Requirements
Education:

• Technical/Engineering Bachelor’s degree with 5 years (or Master’s degree with 3 years) of demonstrated applicable experience.

Experience:

• Managing facilities projects to Product, budget, and timeline commitments
• Managing technical efforts of design firms, contractors, and other vendors
• Using critical metrics for measuring and improving personal work performance
• Managing personal individual effort across multiple concurrent projects
• Managing facilities workstream as part of a large project
• Managing vendor selection using multiple proposals and quotes (use of decision matrix preferred)
• Managing vendor design, build, and install efforts to ensure overall project success
• Managing projects to applicable international standards (e.g. ISO, CE, FDA, etc.) desired
• Knowledge, Skills, Abilities
• Proficient in MS Office
• Proficient in technical writing including authoring RFPs, RFQs, protocols, reports, and other technical documents
• Medical Device/Biopharmaceutical manufacturing standards (i.e. GMP, FDA, ISO)
• Self-motivated with good problem solving, communication, and coordination skills
• Self-starter with demonstrated history of continuous improvement and drive for results