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Description:
• Documentation of development studies (analysis, author protocols and reports with limited supervision)
• Perform studies supporting New Product Development activities
• Coordinate and submit testing of samples
• Support lab experiments
• Hands on preparation of samples for development studies through process
• Coordinate testing of samples
• Manage ADAPTIV documentation processing: create, submit, approvals
Additional Skills & Qualifications:
- BS in engineering; MS preferred - three years of experience in medical device or pharma, material science, chemical engineering / regulated space.
- Three years of experience with documentation of development studies.
About Actalent
Actalent is a global leader in engineering and sciences services and talent solutions. We help visionary companies advance their engineering and science initiatives through access to specialized experts who drive scale, innovation and speed to market. With a network of almost 30,000 consultants and more than 4,500 clients across the U.S., Canada, Asia and Europe, Actalent serves many of the Fortune 500.
Diversity, Equity & Inclusion
At Actalent, diversity and inclusion are a bridge towards the equity and success of our people. DE&I are embedded into our culture through:
- Hiring diverse talent
- Maintaining an inclusive environment through persistent self-reflection
- Building a culture of care, engagement, and recognition with clear outcomes
- Ensuring growth opportunities for our people
The company is an equal opportunity employer and will consider all applications without regard to race, sex, age, color, religion, national origin, veteran status, disability, sexual orientation, gender identity, genetic information or any characteristic protected by law.
If you would like to request a reasonable accommodation, such as the modification or adjustment of the job application process or interviewing process due to a disability, please email actalentaccommodation@actalentservices.com for other accommodation options.
