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Principal Scientist

Chemence Medical, Inc.

Alpharetta (GA)

On-site

USD 105,000 - 131,000

Full time

8 days ago

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Job summary

A leading company in medical equipment manufacturing is seeking a Principal Scientist II to contribute as a technical expert. This role involves leading research and development efforts for innovative products, ensuring compliance with safety and quality standards, and mentoring junior scientists. Ideal candidates will possess a Ph.D. and extensive experience in the field.

Benefits

Medical insurance
Vision insurance
401(k)
Disability insurance
Tuition assistance

Qualifications

  • 10+ years of experience developing medical devices and adhesives.
  • In-depth understanding of adhesive curing mechanisms.
  • Experience with the Product Development Process and Design Controls.

Responsibilities

  • Conduct research and development for new and existing products.
  • Develop and validate new test methods as necessary.
  • Mentor and train junior level scientists and technicians.

Skills

Analytical skills
Critical thinking
Problem-solving
Teamwork
Leadership

Education

Ph.D. in chemistry, polymer chemistry, engineering, materials science, or related discipline

Job description

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Direct message the job poster from Chemence Medical, Inc.

Summary:

As a Principal Scientist II, you are considered a technical expert for Chemence. Your main objective is to contribute to the company’s products, profitability and markets by participating in technical program research for new and existing products and processes consistent with business goals and priorities. This activity requires interfacing with other departments, reading technical literature, planning and conducting experiments and occasionally leading the activities of lower-level employees.

Key Duties and Responsibilities:

Reasonable accommodations may be made to enable individuals with disabilities to perform the essential functions

  • Maintain knowledge of technical developments, which could contribute to or be a competitive threat to project objectives.
  • Maintain compliance with the Quality Manual, Safety Policy and other procedures.
  • Develop and validate new test methods as necessary.
  • Identify and innovate new technologies that could be applied in the adhesive space.
  • Present and communicate new ideas effectively to upper management to make the case for investment.
  • Develop, improve and customize products, equipment, formulas, processes and test methods for new products identified by sales and marketing.
  • Provide specifications and appropriate testing for new incoming raw materials and finished products as required.
  • Review product specifications and performance requirements to determine adequate design of products to meet these requirements.
  • Conduct Research and development efforts to enhance current products or qualify alternative vendors or materials.
  • Assist in the resolution of concerns assigned by Quality for goods and processes.
  • Maintain laboratory to cGMP and GLP requirements as necessary.
  • Write technical reports and prepare presentation/talk for technical conference and proceedings.
  • Plan and conduct research and development programs arising from approved Technical Inquires.
  • Maintain an awareness of technical developments, intellectual property, and compliance regulations relating to areas of interest to the company. Pursue patent applications or maintain proprietary information as appropriate.
  • Technology transfer of optimized formulation processes and/or medical device design to Process Technology team.
  • Mentor and train junior level scientists and technicians.

Qualifications, Education and/or Experience Required:

  • Ph.D. in chemistry, polymer chemistry, engineering, materials science, or related discipline
  • 10+ years of experience developing medical devices and adhesives for target applications and markets.
  • In-depth understanding of adhesive curing mechanism and structure-process-property relationships of components and adhesive products.
  • Experience and knowledge in stage-gate process, computer literacy with knowledge of cGMP, and ISO requirements preferred.
  • Experience in medical device product development process and scale-up activities (design verification and design validation)
  • Proven track record of new technology development and technology transfer (invention) activities
  • Experience with the Product Development Process, Design Controls, and Change Controls for regulated and non-regulated industries
  • Experience with Human Factors/Usability Engineering (preferred, not required)
  • Experience in fundamental failure analysis methodology for a root cause analysis.
  • Strong analytical, critical thinking, and problem-solving skills.
  • Solid teamwork and leadership skills

Language Skills:

Physical Demands:

  • Position requires walking, standing for prolonged periods, occasionally required to sit, climb, or balance, stoop, kneel, crouch or crawl. May frequently lift and/or move up to 10 pounds and occasionally lift and/or move up to 15 pounds.
  • Non-temperature-controlled warehouse, non-temperature-controlled production floor, temperature-controlled office.

Other Duties:

  • Please note this job description is not designed to cover or contain a comprehensive listing of activities, duties or responsibilities that are required of the employee for this job. Duties, responsibilities, and activities may change at any time with or without notice.

AAP/EEO Statement:

  • CHEMENCE provides equal employment opportunities to all employees and applicants for employment and prohibits discrimination and harassment of any type without regard to race, color, religion, age, sex, national origin, disability status, genetics, protected veteran status, sexual orientation, gender identity or expression, or any other characteristic protected by federal, state, or local laws. This policy applies to all terms and conditions of employment, including recruiting, hiring, placement, promotion, termination, layoff, recall, transfer, leaves of absence, compensation, and training.
Seniority level
  • Seniority level
    Mid-Senior level
Employment type
  • Employment type
    Full-time
Job function
  • Job function
    Research, Analyst, and Information Technology
  • Industries
    Medical Equipment Manufacturing

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Inferred from the description for this job

Medical insurance

Vision insurance

401(k)

Disability insurance

Tuition assistance

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