About The Role

Overview

Ensures compliance with applicable standards and regulatory requirements (e.g., FDA, ISO)
Leads laboratory-based quality activities, including hand on experience with Test Method Validation (TMV), Design Verification (DV), and product testing
Authors, executes, and reviews test plans protocols, and reports to support product development
Execute hands-on laboratory testing, data analysis, and technical investigations
Collaborates with Design Engineering, Regulatory, and Laboratory staff to ensure testing activities are appropriately planned, executed, and documented
Supports design controls, risk management, and other quality activities as needed

Responsibilities

Author, review, and execute TMV protocols and reports
Develop and execute Design Verification plans, protocols, and reports
Support hands-on verification and validation testing activities
Analyze test data, document results, and communicate findings to project teams
Investigate test failures, deviations, and nonconformances; support root cause analysis and corrective actions
Ensure accuracy, completeness, and traceability of testing and validation documentation
Review and approve quality and testing documentation in accordance with development procedures
Support project teams and laboratory on quality-related activities
Provide support for other quality activities, including design controls and risk management documentation

Requirements

Bachelor’s or Master’s degree in Engineering, Science or related field
2-4 years of experience in QC, laboratory, or quality departments within medical device or pharmaceutical industries
Working knowledge of relevant regulations and industry standards (FDA 21 CFR 820, ISO 13485, etc.)
Proven experience authoring and executing TMV and DV documentation
Strong hands-on laboratory testing and data analysis experience
Strong technical writing and documentation skills
Experience with statistical analysis tools such as Minitab, JMP, or equivalent.
Self-motivated with good communication and organization skills

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 www.nemera.netKnow 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 : $95,000- $115,000 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.