Senior Product Development Engineer -Mechanical Engineering (Hybrid Boston)

Haemonetics Corp; Boston (MA); On-site; USD 78,400 - 133,400; Full time

Benefits offered by this job

401(k) with up to 6% employer match

Employee stock purchase plan

Flexible time off for salaried employees

Job summary

Haemonetics Corp in Boston, MA is seeking a Senior Biomedical Product Development Engineer to lead the mechanical design of disposable components for the TEG6s IVD system. This role is vital for ensuring product performance and compliance throughout the lifecycle.

The ideal candidate will have at least 5 years of experience in medical device development, a strong background in engineering principles, and proficiency in CAD systems. The position offers a competitive compensation package and opportunities for professional growth in a dynamic team environment.

Qualifications

• Minimum of 5+ years in medical device, IVD, or regulated industry product development.
• Expertise in developing disposable components through full lifecycle.
• Prior involvement in FDA 510(k), PMA, or CE submission processes.

Responsibilities

• Lead the lifecycle of disposable device components from concept development to verification.
• Develop and execute verification and validation test protocols.
• Ensure compliance with FDA and ISO requirements.

Skills

Design for high volume manufacturing

GD&T capabilities

Data analysis and DOE methodologies

Collaboration with cross-functional partners

Education

Bachelor's degree in Bioengineering or Mechanical Engineering

Tools

SolidWorks CAD

MS Project

PLM systems

Job description

Job Details

Job Summary

We are seeking an experienced and creative-thinking Senior Biomedical Product Development Engineer to join our multidisciplinary Research & Development Systems Engineering team in Boston, MA. In this role, you will serve as the primary owner of the mechanical design and functional performance of disposable components used within the TEG6s in vitro diagnostic (IVD) system. You will play a critical role across the full product lifecycle—supporting both new product development and sustaining engineering initiatives—while collaborating closely with assay development, manufacturing, quality, regulatory, system hardware, clinical, and commercial teams to ensure robust product performance and successful market introduction. Your work will directly influence the accuracy, reliability, and usability of a platform used globally in clinical decision‑making.

Key Responsibilities

Design & Technical Leadership

• Lead the complete lifecycle of disposable device components, including concept development, detailed design, integration, and verification.
• Translate user and system needs into engineering requirements, specifications, and risk documentation.
• Address complex design challenges balancing innovation, manufacturability, and timeline constraints.

Execution, Testing & Compliance

• Develop and execute verification and validation (V&V) test protocols; analyze performance data to confirm design functionality.
• Plan and conduct feasibility and prototype studies supporting both new development and sustaining efforts.
• Ensure compliance with internal SOPs and external standards including FDA QSR, CE Marking, and ISO requirements.
• Generate high‑quality documentation for design controls, investigations, and regulatory submissions (510(k), PMA, technical files).

Cross Functional Collaboration & Mentorship

• Partner with QA, DQ, SQ, Clinical, Regulatory, Marketing, Procurement, and Manufacturing teams to support product success.
• Provide mentorship and technical guidance to junior engineers.
• Work directly with global suppliers to support part development, validation, and production.

Qualifications

• Bachelor's degree in Bioengineering, Mechanical Engineering, or related technical field.
• Minimum of 5+ years in medical device, IVD, or regulated industry product development.
• Strong experience developing disposable components or capital equipment through full lifecycle (concept production).
• Expertise in design for high volume manufacturing, cost optimization, and tolerance analysis.
• Proficiency with SolidWorks CAD, BOM management, and PLM systems.
• Knowledge of plastics and metals fabrication (injection molding, lamination, laser welding, additive manufacturing, bonding).
• Prior involvement in FDA 510(k), PMA, or CE submission processes.

Preferred Qualifications

• Experience with microfluidic, cartridge‑based, or disposable diagnostic systems.
• Hands‑on iterative prototyping and test‑driven design experience.
• Proficiency with data analysis and DOE methodologies.

Skills & Competencies

• Strong GD&T capabilities for drawing creation and interpretation.
  Familiarity with project management tools (MS Project, Smartsheet).
• Working knowledge of FDA QSR, CE Marking, and ISO quality systems.
• Effective collaboration with cross‑functional partners and external suppliers.
• Basic wet‑lab proficiency supporting testing and system development.

What This Role Offers

• Ownership of critical components within a globally deployed diagnostic platform.
• Opportunities to work at the intersection of engineering, microfluidics, and clinical diagnostics.
• Collaboration with a highly skilled and mission‑driven technical team.
• Direct contribution to improving patient outcomes worldwide.

EEO Policy Statement

EEO Policy Statement

Pay Transparency & Benefits

Pay Transparency: The base pay actually offered to the successful candidate will take into account, without limitation, the candidate's location, education, job‑knowledge, skills, and experience in prior relevant roles. Incentives may also be provided as part of Haemonetics' employee compensation. For sales roles, employees will be eligible for sales incentive (i.e., commission) under the applicable plan terms. For non‑sales roles, employees will be eligible for a discretionary annual bonus, the target amount of which varies based on the applicable role, to be governed by the applicable plan terms. Employees may also be eligible to participate in the Company's long‑term incentive plan, with eligibility and target amount dependent on the role.

In addition to compensation, the Company offers a competitive suite of benefits to its employees, including without limitation, a 401(k) with up to a 6% employer match and no vesting period, an employee stock purchase plan, flexible time off for salaried employees and, for hourly employees, accrual of three to five weeks' vacation annually (based on tenure), accrual of up to 64 hours (annually) of paid sick time, paid and/or floating holidays, parental leave, short‑ and long‑term disability insurance, tuition reimbursement, and/or health and welfare benefits.

Depending on your location, you may be eligible for more detailed information related to the compensation and benefits related to this job posting. If you believe you may be entitled to such information by law, you may contact 1‑781‑348‑7777, Monday through Friday, 7:30 a.m. - 5 p.m. ET or email [e-mail].

The base salary range for this role is:

$78,400.00-$133,400.00/Annual