Technology Transfer Project Manager I
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![]() United States, Utah, Salt Lake City | |
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Technology Transfer Project Manager I
Location: Salt Lake City, UT, United States Share:
share to e-mail Share on Facebookshare to facebook Tweetshare to twitter Share on LinkedInshare to linkedin Apply Now > A world leader in the field of in vitro diagnostics for more than 60 years, bioMerieux provides diagnostic solutions which determine the source of disease and contamination to improve patient health and ensure consumer safety. In North America we have more than 6,200 team members across 11 sites or subsidiaries, including Salt Lake City-based BioFire Diagnostics and one subsidiary in Montreal, Canada. Come and join a family-owned global company with a long-term vision, and a human-centered culture. Description Position Summary Implements and administers multiple projects of low to medium complexity, each potentially consisting of sub-projects. Organizes cross-functional activities to ensure project completion while adhering to regulations, scope, and schedule requirements. Acts as an in-house consultant for project evaluation needs. Plans and directs implementation efforts, evaluating the scope and impact of new products and processes, and providing feedback on proposed changes. Primary Duties * Ensures all work complies with company policy and adheres to bioMerieux's Quality System guidelines. * Coordinates efforts for the transfer (industrialization) of instrument products and/or manufacturing equipment from R&D to Instrument Manufacturing. * Lead and monitor projects, applying best practices throughout initiation, planning, development, implementation, and launch. Ensure projects meet quality, scope, and schedule objectives while maintaining regulatory standards and quality system requirements. * Plan and direct cross-functional change implementation, including evaluating impact, risks, and scope for new and existing products and processes. * Act as the point of contact and transfer expert for assigned projects. Provide technical support and improvements to existing products and processes. * Ensure consistent practices are maintained throughout all phases of the project life cycle. * Schedule meetings, create agendas, and document meeting minutes, correspondence, and presentations. * Develop, establish, and maintain accurate project timelines. * Coordinate updates to manufacturing process documents, including Standard Operating Procedures, Batch Records, risk assessments, specification documents, and drawings. * Communicate, prepare, and present reports, summaries, and analyses to support project status and progress. * Create and maintain relevant project documentation throughout the project lifecycle. * Execute high-quality, integrated, cross-functional plans for projects. * Interact with and coordinate activities between Engineering R&D, Program Management, Supply Chain, Purchasing, Materials Management, Quality Assurance, Software, Service, Manufacturing, and Regulatory departments. * Perform other duties as assigned. Supplemental Data * This position is an individual contributor role with no supervisory responsibilities. * Occasional travel to vendor locations, both domestically and internationally, may be required. Training, Education and Experience * A bachelor's degree in chemistry, biology, physics, math, engineering, or a closely related field is required. Significant related experience may be considered in lieu of a degree. * An MBA and/or PMP certification from the Project Management Institute is desired but not required. * At least three years of relevant work experience. * Minimum of two years of project management or related experience. * A Master's degree or PhD in a related field may substitute for the required project management experience. Preferred: * At least three years of experience working in ISO 9001/13485 and/or cGMP/cGLP compliant environments. Knowledge, Skills and Abilities Required: * Ability to work effectively both independently and as part of a team. * Strong time management skills to efficiently handle multiple projects simultaneously. * Proficiency in writing detailed reports and procedures. * Excellent documentation practices, organizational skills, and attention to detail. * Ability to define problems, collect relevant data, establish facts, and draw valid conclusions. * Exceptional written and verbal communication skills, along with strong interpersonal abilities. * Proficiency with MS Office Suite, including Word, Excel, and PowerPoint. * Strong decision-making abilities. * Ability to elicit cooperation and coordinate activities across multiple departments. * Ability to prioritize and execute tasks effectively in a fast-paced environment. * Strong problem-solving skills. Preferred: * Strong statistical and analytical skills. * Familiarity with project management tools such as Asana and Visio. Working Conditions and Physical Requirements * Ability to remain in a stationary position, often standing or sitting, for prolonged periods. * General physical requirements found in an office setting. * Minimal Travel 1% of time Please be aware that recruitment related scams are on the rise. Fraudulent job postings are being placed on other websites, and individuals posing as bioMerieux Talent Acquisition team members are reaching out via email or text message in an attempt to collect your personal and confidential information. In some cases, these scammers are also conducting bogus interviews prior to extending fraudulent offers of employment. Beware of individuals reaching out using general phone numbers and non-bioMerieux email domains (i.e. Hotmail.com, Gmail.com, Yahoo.com, etc.). If you are concerned that an interview experience or offer of employment might be a scam, please make sure you are searching for the posting on our careers site https://careers.biomerieux.com/ or contact us at recruitment@biomerieux.com. BioMerieux Inc. and its affiliates are Equal Opportunity/Affirmative Action Employers. All qualified applicants will receive consideration for employment without regard to race, color, religion, sex, sexual orientation, gender identity, national origin, age, protected veteran or disabled status, or genetic information. Please be advised that the receipt of satisfactory responses to reference requests and the provision of satisfactory proof of an applicant's identity and legal authorization to work in the United States are required of all new hires. Any misrepresentation, falsification, or material omission may result in the failure to receive an offer, the retraction of an offer, or if already hired, dismissal. If you are a qualified individual with a disability, you may request a reasonable accommodation in BioMerieux's or its affiliates' application process by contacting us via telephone at (385) 770-1132, by email at recruitment@biomerieux.com, or by dialing 711 for access to Telecommunications Relay Services (TRS). Share:
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