What are the responsibilities and job description for the Scientist / Chemist position at MillenniumSoft Inc?
Position : Scientist / Chemist
Location : Franklin Lakes, NJ
Duration : 12 months contract
Start Time : 8:00 AM
End Time : 5:00 PM
Total Hours/week : 40.00
Qualifications
Location : Franklin Lakes, NJ
Duration : 12 months contract
Start Time : 8:00 AM
End Time : 5:00 PM
Total Hours/week : 40.00
Qualifications
- M.S. or PhD in Chemical Engineering, Materials Science/Engineering, Polymer Science/Engineering or related polymer field
- At least 7 years of polymer experience
- Experience with polymer surface modification is a plus
- Knowledgeable in the area of polymer structure processing property relationships
- Demonstrated knowledge of physical property testing and polymer characterization techniques
- Experience with polymeric product manufacturing processes preferred
- Experience working in cross-functional product development teams, in the area of medical devices is preferred
- Technical writing experience required
- Prior experience working in medical device field or regulated industry a plus
- Capable of making practical assumptions with engineering justifications, where needed
- Experience with collecting and recording data, interpreting data and writing technical reports in a manner consistent with QSR, ISO, and GMP guidelines
- Experience with laboratory testing and equipment, such as Instrons
- Experience in delivering on-time to an existing project plan
- Ability to evaluate and summarize test results in written reports, including observations and discussion on findings and present results to team members orally and in writing
- Experience with statistical analysis and methods within Minitab and Microsoft Excel
- Hands on-experience operating and programming of material test equipment
- Self-initiator, results driven, and action- and detail-orient
- Experience with working in a product/design qualification/testing lab within R&D that supports development of medical device products
- Demonstrated experience with all phases of the Design Control process in the context of FDA regulation and understanding of disciplined product development processes, regulatory and quality requirements for medical products
- Excellent interpersonal, written and verbal communication, and influencing skills
- Strong technical judgment and problem solving skills
- Work independently and/or cross-functionally to map formulation - material property relationships
- Create prototypes and write laboratory testing protocols
- Provide technical support in characterization of material properties - mechanical, rheological, and surface
- Communication of results in both written and oral formats, including the maintenance of project documentation that meets regulatory requirements