Zoetis

Diagnostics On-Market Product Engineering Lead

US
USD 123k - 123k
R Assembly
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Description

Role Description

The DIAGNOSTICS ON-MARKET PRODUCT ENGINEERING MANAGER will work as a member of the research and development team to provide engineering oversight for improvements and updates to diagnostic devices throughout the on market product life cycle. The On-Market Product Engineering Manager will contribute throughout the Stage Gate development process with increasing involvement as the product reaches the Ready to Manufacture (RTM) milestone.  After RTM the On-Market Product Engineering Manager is responsible for guiding all design changes including product design, development, testing, and integration of electro-mechanical, thermal, and optical sub-systems into on-market diagnostic products. The On-Market Product Engineering Manager will apply best practice development strategy and advanced technical concepts to solve complex problems, distilling them down to effective product updates which strike the balance of functionality, usability and minimizing manufacturing and repair impacts. The On-Market Product Engineering Manager will be guided by a stage gate development process prior to RTM and an engineering change control process after RTM. The On-Market Product Engineering Manager will be expected to resolve complex technical challenges that arise during product the product life cycle.

Essential Duties and Responsibilities:

  • Carry the leadership role of the product support engineering effort with Manufacturing Transfer, Global Manufacturing & Supply, and Quality such that product commercialization is achieved through product lifecycle and supply base relationships.
  • Lead and develop a Product engineering team team
  • Responsible for proper engineering oversight of R&D (Engineering) product design change release & collaborative change management process into Product Lifecycle Management release systems (PLM)
  • Grow and maintain technical knowledge related to technology and product development of in-vitro diagnostic devices. Including developing product SMEs in multiple engineering disciplines.
  • Work with Manufacturing to consider high volume assembly process in design changes and update/maintain product design documents (DFx, DFMEA, FEA).  Analyze and recommend improvements of production processes and methods to facilitate cost reduction and quality improvement.
  • Participate in the oversight of Contract Product Manufacturing (external partner/OEM’s) as required
  • Develop an understanding and maintain and/or revise electro-mechanical and thermodynamic control sequences in the product requirements, while understanding the interface to electrical control systems and underlying biological process needs for all design changes and updates.
  • Prepare documentation for change control activities and efforts.
  • Develop and implement mechanical, electrical, and system design changes, perform sensitivity analysis, timing analysis, or other design analysis as required.
  • Assessment of system level risks, and proposing, evaluating, and implementing mitigations for all design changes.
  • Ensure designs continue to meet and exceed product specifications, regulatory requirements, and international standards after design changes.
  • Proficient in communicating complex technical situations in an understandable way to non-technical collaborators.
  • Work cross functionally in a global organization, deploy engineering best practices in the context of a change control process, and navigate satisfying product technical specifications as prescribed by customer and market requirements for all design changes.
  • Participate in system engineering for complex electromechanical/thermodynamic/optical systems to update product specifications and controls interactions of each system.
  • Analyze and recommend corrective actions in case of any design issues.
  • Extensive interaction with suppliers in design, analysis, and other technical liaison requirements.

Requirements:

  • B.S. in Mechanical/Electrical Engineering, MSME/MSEE. Minimum of 15 years demonstrated engineering experience in a complex engineered product environment.  Quality Management System understanding a must.
  • Experience in developing animal health devices or human health devices are a plus
  • Experience working with Design and Implementation teams, Operations (Manufacturing, Quality, Metrology) and suppliers from an engineering, technical perspective.
  • 5 plus years of experience in people management leading, managing, developing engineering team members
  • Technical Skill Requirements: SAP or similar understanding, Engineering Change Management in PLM environment
  • Root cause analysis techniques and robust documentation to support engineering best practices.
  • Demonstrated proficiency in engineering specifications and design for electromechanical software driven equipment.
  • Knowledge of materials and manufacturing/construction principles.

The following base pay range reflects the anticipated base pay for this position if a selected candidate were to be located in [California]. Base pay may vary based on location and other factors.

 

Base Pay Range: $123,000 $176,000

[This position is eligible for short-term incentive compensation.] [The position is also eligible for long-term incentive.]

 

We offer a competitive and comprehensive benefits package, which includes healthcare, dental coverage, and  retirement savings benefits along with paid holidays, vacation and disability insurance.

Full time

Regular

Colleague

Any unsolicited resumes sent to Zoetis from a third party, such as an Agency recruiter, including unsolicited resumes sent to a Zoetis mailing address, fax machine or email address, directly to Zoetis employees, or to Zoetis resume database will be considered Zoetis property. Zoetis will NOT pay a fee for any placement resulting from the receipt of an unsolicited resume.

Zoetis will consider any candidate for whom an Agency has submitted an unsolicited resume to have been referred by the Agency free of any charges or fees. This includes any Agency that is an approved/engaged vendor but does not have the appropriate approvals to be engaged on a search.

Zoetis is committed to equal opportunity in the terms and conditions of employment for all employees and job applicants without regard to race, color, religion, sex, sexual orientation, age, gender identity or gender expression, national origin, disability or veteran status or any other protected classification. Disabled individuals are given an equal opportunity to use our online application system. We offer reasonable accommodations as an alternative if requested by an individual with a disability. Please contact Zoetis Colleague Services at zoetiscolleagueservices@zoetis.com to request an accommodation. Zoetis also complies with all applicable national, state and local laws governing nondiscrimination in employment as well as employment eligibility verification requirements of the Immigration and Nationality Act. All applicants must possess or obtain authorization to work in the US for Zoetis. Zoetis retains sole and exclusive discretion to pursue sponsorship for the acquisition or maintenance of nonimmigrant status and employment eligibility, considering factors such as availability of qualified US workers. Individuals requiring sponsorship must disclose this fact. Please note that Zoetis seeks information related to job applications from candidates for jobs in the U.S. solely via the following: (1) our company website at www.Zoetis.com/careers site, or (2) via email to/from addresses using only the Zoetis domain of “@zoetis.com”. In addition, Zoetis does not use Google Hangout for any recruitment related activities. Any solicitation or request for information related to job applications with Zoetis via any other means and/or utilizing email addresses with any other domain should be disregarded. In addition, Zoetis will never ask candidates to make any type of personal financial investment related to gaining employment with Zoetis.

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