Senior Scientist

GForce Life Sciences • united states, united states, us • 1m ago

Responsibilities

Participate in working groups to establish the identification of PFAS chemicals in existing product portfolio and recommend effective, sustainable and documented alternative materials that meet international, federal, state and local product environmental regulations and product standards compliance, as well as design requirements
Documentation and maintenance of records used to track and report environmental compliance and environmental stewardship programs
Assess emerging environmental trends and new and changing Product Environmental Compliance regulations to provide leadership in driving changes into both new product development and product sustaining plans
Consult on selection and testing of materials to determine whether they meet specifications of mechanical strength, strength-weight ratio, ductility, magnetic and electrical properties, and resistance to abrasion, corrosion, heat and cold
Respond to questionnaires from tenders, customers, and special interest groups ranging from environmental stewardship initiatives to material content of products
Respond to environmental questionnaires, inspections or audits from global regulatory authorities

Basic Qualifications

Bachelor’s degree in material science, chemical, mechanical or electrical engineering
5 years of design experience in materials identification, selection, and testing

Preferred Qualifications

Master’s degree in material science or chemical engineering
5 years’ experience in local, state, federal and international Product Environmental compliance practice
Working knowledge of regulations and best practices in the following areas: RoHS, REACH, WEEE, Battery, Packaging, Proposition 65, EU MDD, and EU-MDR
Experience establishing, training, and supporting Quality Systems processes in support of Product Environmental compliance
Design or Manufacturing background preferred
Organized, possessing strong computer hardware and software skills; proficient in MS Office suite
Prior experience with FDA and medical device manufacturing requirements

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