Sr Specialist R&D
REMOTE- Illinois, United States
Job Summary
Responsible for contributing to the development of new products and technologies within the R&D group. The role will be a subject matter expert in a specific support area and will facilitate project needs related to that knowledge. Areas of focus may include performance testing, chemical characterization, stability testing, biocompatibility, toxicological assessments, risk assessments, etc.Job Description
Responsibilities:
Plan and execute or otherwise facilitate testing required in support of a product claim.
Author, review, and approve test protocols and reports.
Track, compile, and review all results needed in support of product requirements and regulatory submissions such as 510k’s, CE technical files, and ANDA/NDAs.
Compile technical justifications and data summaries in support of product claims.
Identify and support the development of product requirements, performance attributes, and quality specifications. Coordinate verification and validation activities.
Review and trend results to identify product or process improvement opportunities and lead implementation efforts.
Ensure compliance of all data collection activities with applicable regulatory requirements.
Act as a lead for internal and external audits.
Compile risk assessments, identify gaps, and propose solutions.
Lead process improvement, CAPA, OOS investigations, and data trending activities.
Represent Medline on various ASTM/AAM/ISO technical committees and contribute to the development of new test standards.
Qualifications:
Bachelor’s degree in Chemistry, Biology or related science field.
At least 4 years of experience in a medical device or pharmaceutical related field.
Knowledge of FDA requirements and experience with FDA interactions as part of the 510k/ANDA/NDA approval processes.
Knowledge of CE technical files.
Experience with risk assessment and root cause analysis.
Experience in solving practical problems and dealing with a variety of concrete variables in situations where only limited standardization exists.
Experience communicating with internal and external business partners and cross functional teams with various audiences.
Experience in project management skills, with ability and proven track record to plan, manage and develop strategic initiatives to successful goal completion.
Self-starter, independent worker, detail oriented with critical thinking and excellent organizational, analytical and problem solving skills.
Strong time management skills to prioritize, organize track details and meet deadlines for multiple projects with varying completion dates.
Ability to influence and motivate others to drive results in a multi-location and matrixed environment.
Position may require travel up to 10% of the time for business purposes (domestic and international).
Medline Industries, LP, and its subsidiaries, offer a competitive total rewards package, continuing education & training, and tremendous potential with a growing …
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Illinois May require travel
Benefits/Perks401K contributions Competitive total rewards Competitive total rewards package Continuing education Continuing education & training Employee Assistance Program Health insurance Life and disability Medical Paid Time Off Training
Tasks- Conduct risk assessments
- Develop new products
- Ensure compliance
- Facilitate testing
- Implement process improvements
- Lead audits
510k AAM Access Analytical ASTM Biocompatibility CAPA Compliance Critical thinking Cross-functional Communication Data trending FDA ISO NDA Organization Organizational Performance Testing Problem-solving Process Improvement Project Management R R&D Regulatory Submissions Risk Assessment Risk assessments Root Cause Analysis Stability testing Technical Writing Time Management Training
Experience4 years
EducationBachelor's degree in biology Bachelor's degree in chemistry Related Field
TimezonesAmerica/Anchorage America/Chicago America/Denver America/Los_Angeles America/New_York Pacific/Honolulu UTC-10 UTC-5 UTC-6 UTC-7 UTC-8 UTC-9