Laboratory Project Specialist

Position Summary

We are seeking an experienced Lab Project Specialist to lead the planning development and execution of verification activities for medical device products. This individual will serve as a technical expert in device testing design inputs risk analyses and product requirements into robust verification strategies and test methods.

The ideal candidate possesses a strong engineering background understands how medical devices function from both a design and user perspective and can independently determine what testing is required to demonstrate that design requirements have been met. This role works closely with R&D Lab Quality Regulatory Affairs and external partners throughout the product development lifecycle.

Key Responsibilities

Design Verification 

• Develop and execute design verification strategies for new and existing medical devices.
• Review product requirements design inputs and risk analyses to determine appropriate verification activities.
• Create verification protocols test plans acceptance criteria and reports in compliance with applicable design control requirements.
• Ensure objective evidence is generated to demonstrate compliance with design requirements.

Test Method Development and Test Execution

• Design develop optimize and validate test methods for mechanical functional usability environmental reliability and performance testing.
• Identify and implement appropriate measurement systems instrumentation fixtures and data acquisition methods.
• Evaluate test method capability repeatability and reproducibility (e.g. GR&R).
• Develop custom test equipment and fixtures as needed.
• Support TMV and testing execution.

Data Analysis and Technical Reporting

• Analyze test data using statistical and engineering methods.
• Support root cause analysis and recommend corrective actions.
• Prepare clear technical reports and present findings to project teams and management.

Cross-Functional Collaboration

• Collaborate with Design Engineering Quality Regulatory Affairs and Lab staff.
• Coordinate testing activities with external laboratories consultants and suppliers.
• Mentor junior engineers and provide leadership in verification and testing practices.
• Support overall project planning from a testing strategy perspective.

Compliance and Quality

• Ensure verification activities comply with applicable standards guidance documents and internal procedures.
• Participate in Design Control Risk Management and Design History File (DHF) activities.
• Expertise in ISO 13485 ISO 14971

Qualifications :

Required Qualifications

• Bachelors degree in Mechanical Engineering Biomedical Engineering Electrical Engineering Systems Engineering or related discipline.
• 3 years of experience in medical device development verification testing or systems engineering.
• Demonstrated experience developing verification strategies and executing design verification programs.
• Strong understanding of medical device design controls and product development processes.
• Experience developing test methods and analyzing data.
• Excellent technical writing and communication skills.
• Ability to independently assess designs and determine appropriate verification approaches.
• Ability to work in a lab and/or clean room environment requiring PPE

Preferred Qualifications

• Experience with inhalation drug delivery combination products surgical diagnostic or other complex medical devices.
• Knowledge of risk management and failure analysis methodologies.
• Experience with statistical analysis tools such as Minitab JMP or equivalent.
• Familiarity with IEC 60601 ISO 11608 or other applicable medical device standards.
• Experience managing external test laboratories and contract development partners.

Additional Information :

Why Join Nemera

At Nemera we prioritize patients when creating drug delivery devices understanding that accurate dosing and ergonomics are crucial for treatment adherence. Joining Nemera means becoming part of a team that enjoys working together and consistently delivers on its commitments. We take pride in our work because it improves patients lives.

We look forward to receiving your application (resume submitted in English is appreciated). We offer varied jobs job in an international group if you want to discover more about Nemera please look at our website someone at Nemera We have a Referral Program so be sure to have them submit you as a referral prior to applying for this position

POSITION RANGE: $85000- $115000 USD Salaried (This is the range that we in good faith believe is the range of possible compensation for this role at the time of this posting. This range may be modified in the future.)

For US Benefits CLICK HERE.

Nemera is an equal opportunity employer and does not discriminate against any person on the basis of race religion color gender gender identity sexual orientation age national origin disability veteran status or any other protected class indication. This company is required by federal law to hire only persons who can establish they are eligible to work in the United States.

Remote Work :

No

Employment Type :

Full-time