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Senior Biocompatibility Specialist
Zimmer Biomet —Shannon, County Clare
- Full-time
- Doctoral degree
- Presentation skills
- Manufacturing
- Wellness program

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Senior Biocompatibility Specialist
Zimmer Biomet —Shannon, County Clare
Resource for biological evaluation of changes to current manufacturing processes as well as new manufacturing processes for new product development.

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Senior Biocompatibility Specialist

Zimmer Biomet -
Shannon, County Clare

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Job details

Full-time

Benefits

Wellness program

Qualifications

Doctoral degree
Presentation skills
Manufacturing
Leadership
Communication skills

Full job description

At Zimmer Biomet, we believe in pushing the boundaries of innovation and driving our mission forward. As a global medical technology leader for nearly 100 years, a patient’s mobility is enhanced by a Zimmer Biomet product or technology every 8 seconds.

As a Zimmer Biomet team member, you will share in our commitment to providing mobility and renewed life to people around the world. To support our talent team, we focus on development opportunities, robust employee resource groups (ERGs), a flexible working environment, location specific competitive total rewards, wellness incentives and a culture of recognition and performance awards. We are committed to creating an environment where every team member feels included, respected, empowered and recognised.

What You Can Expect

This position is responsible for planning, organizing, and conducting biological safety risk assessments on medical devices in accordance with current regulations. Frequent communication with internal and external customers is expected. Both teamwork and individual contributions are valued.

How You'll Create Impact

Biological Safety Risk Assessments and development of testing strategies for medical devices
Resource for biological evaluation of changes to current manufacturing processes as well as new manufacturing processes for new product development
Internal technical document creation and approval
Support complaints investigations, CAPAs, and other general technical support duties required within the team
Create Technical Reviews, specifications and other mandatory documents for regulatory submissions
Review and preparation of procedures to keep pace with standards development
Represent the company via presentations to groups of experts, societies, regulatory bodies and at international meetings.
Help to develop and generate material for staff training and data presentations
Maintain relevant scientific and medical knowledge by attending conferences, courses and meetings
Educate internal colleagues across departments and divisions in the area of biological safety evaluations, risk assessments, and chemical characterization.
Provides support for key opinion leaders

What Makes You Stand Out

Has shown outstanding competencies as subject matter expert
- In depth knowledge of ISO 10993 standards and EU MDR
- Working knowledge of analytical chemistry
- Has a comprehensive record of external training in area of competence
- Prior experience with risk assessment of manufacturing materials
Has proven competency in presenting subject matter to expert groups and key opinion leaders in a clear and convincing matter.
Has experience in conveying complex scientific topics in a clear and comprehensible fashion.
Able to effectively resolve conflict between two or more parties
Strong problem solving skills. Able to analyze all aspects of a situation, identify potential solutions, and implement the best solution in a timely manner
Goes beyond existing knowledge base and expands our understanding, methods, and procedures, leaving a base for others to utilize and build upon (trailblazing)
Demonstrates ability to balance needs of all departments to meet customer expectations and project schedules
Demonstrates an ability to utilize resources efficiently
Demonstrated ability to represent the company to accomplish objectives even during disagreements
Is professional, concise, and sensitive in accomplishing objectives. Is able to diplomatically negotiate with a requester regarding what they want in design, process, scope or timetable
Demonstrates strong written and verbal communication skills including presentation skills. Has ability to tailor the information to the audience and answer with confidence and authority scientific questions
Handles discussions of complex topics with confidence
Demonstrates ability to discuss sensitive information with and tailor communication style to listeners’ perspectives, including management, surgeons, and external contacts
Shows leadership skills and initiative

Your Background

Minimum educational requirement is a MS in relevant scientific disciplines, such as biology, chemistry, biomedical engineering, and/or toxicology.
Minimum of 4 years experience in medical device research (Orthopaedic industry preferred) or an equivalent combination of PhD, Postdoctoral, and experience in related field required

EOE/M/F/Vet/Disability

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Senior Biocompatibility Specialist

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