|
|
Help Us Create Tomorrow.
At Biomet Microfixation, we offer an exceptional benefits package, which includes:
- Company paid team member and family medical and dental coverage
- Company paid team member life insurance
- Company match 401(K)
- Short and Long Term disability
- Generous tuition reimbursement program
Thank you for your interest in an employment opportunity with us. Due to the large number of resumes we receive from the Internet, we are only able to accept resumes or applications that are for a specific position posted on this web site. Please review the position titles and the responsibilities of the specific position (by clicking the title) that you are interested in and apply only if your credentials meet the necessary requirements for the position.
Biomet Microfixation is an Equal Opportunity Employer M/F/D/V.
Job Opportunities
Director of Research
Job Summary: The primary responsibility for this position is to design and manage pre-clinical and clinical studies to support development, regulatory approval, and post-market surveillance of innovative new products that anticipate the needs of our customers.
Essential Duties:
- preparation and management of the annual research budget (approximately $1.4M annually),
- design of study protocols,
- preparation and negotiation of research contracts,
- management of compliance to study milestones, evaluation and analysis of study results
- assisting with regulatory document preparation
- management of clinical research organizations.
The secondary responsibilities for this position include:
- management of wet lab facilities,
- chairing monthly Research Committee meetings with upper management
- management/development of two direct reports
Job Specificaitons: -Statistical analysis experience for protocol development and study result evaluation. Involvement in at least one clinical trial to support a PMA/IDE submission to FDA. Knowledge of ISO 13485 requirements.
Skills and Abilities: Educational concentration in biostatistics, epidemiology, and methods in clinical research. Medical Device Manufacturing Knowledge / Background. Prior OR / Surgical Suite Interaction. Education: MS Engineering Discipline, Biomedical, Biochemistry, or Public Health – Epidemiology disciplines. Excellent Problem Solving Skills, Conflict Resolution. Strong interpersonal skills. Business acumen, strategic thinker. High energy & persistent, results oriented. Excellent Communication Skills (verbal, written, presentation).
Education and Experience: Bachelors Degree in Engineering, Biomedical, Biochemistry or Public Health. Pre-clinical and clinical research experience (5 years minimum).
Working Climate: Travel: 20%
Only qualified candidates will be considered for employment for this position. Please send your resume and salary requirements to:
fxjax.hrjobs@biomet.com
OR
Fax 904-741-4407
Sales Representative
Responsibilities: Compiles lists of prospective customers for use as sales leads, based on information from industry ads, trade shows, Internet Web sites, and other sources. Travels throughout assigned territory to call on regular and prospective customers to solicit orders, or talks with customers. Displays or demonstrates product, using samples or catalog, and emphasizes salable features. Prepares reports of business transactions and keeps expense accounts. Works with customer service representatives to keep account activities and literature up to date. Tracks stock levels. Coordinates customer training. Develops and maintains relationships with purchasing contacts. Investigates and resolves customer problems with deliveries. Attends trade shows.
Qualifications: Bachelor's degree (B.A.) from four-year college or university and three years related experience.
Biomet Microfixation is always looking for talented individuals for our Sales force. If you are interested in a career in Biomet Microfixation's Sales division and you meet our qualifications, please send your resume to:
fxjax.hrjobs@biomet.com
OR
Fax 904-741-4407
Senior Product Manager, Brand Mgmt.
The Senior Product Manger, Brand Management is accountable for leading the strategy, design, development and implementation of marketing plans and programs in support of assigned product line strategies and business goals for Biomet Microfixation. Specific responsibilities include: launching products to global regions and ensuring launch metrics are achieved, driving sales of existing product lines via Marketing 4Ps aimed at motivating sales force and end users / customers, global product support / service, maintain deep knowledge of market trends and competitive products / activity, maintaining consistent communication with the sales force, conducting / facilitating sales training, forecasting, SKU management, maintaining P&L for product lines, pricing discipline for product lines, managing and developing Associate Product Managers and / or Product Managers, attend industry conferences and symposia as necessary, and support Biomet Microfixation strategic planning and portfolio planning activities as necessary. The position will report to the Director of Global Marketing and will work closely with colleagues in product management, R&D, Finance, Regulatory, Sales and Operations.
Only qualified candidates will be considered for employment for this position. Please send your resume and salary requirements to:
fxjax.hrjobs@biomet.com
OR
Fax 904-741-4407
Preferred Education: Bachelor's degree required; MBA preferred. A minimum of 3+ years of marketing experience required. Brand management experience preferred. People management experience required. Medical device experience products a plus. Strong analytical / quantitative skills, excellent communication and presentation skills, demonstrated strength in interdepartmental partnering and team management, ability to manage multiple projects simultaneously, and strong PC skills (excel, powerpoint). This position requires up to 35% domestic and/or international travel.
Senior Regulatory Affairs Specialist
Responsibilities:
- Develop and execute regulatory strategies for new and modified products.
- Prepare 510K submissions to obtain and maintain domestic regulatory clearances.
- Provide technical and regulatory guidance to new product development and product management teams.
- Develop and maintain positive relationships with regulatory agency reviewers through oral and written communications regarding pre-submission strategy, regulatory pathway development, testing requirements and follow up of submissions under review.
- Review device labeling and promotional material for compliance with applicable regulations.
Quallifications
- B.S. in scientific discipline
- Minimum of 5 years of Regulatory Affairs medical device industry experience.
- Demonstrated success in the management of device 510k submissions is required; internationa and/or PMA experience a plus.
Only qualified candidates will be considered for employment for this position. Please send your resume and salary requirements to:
fxjax.hrjobs@biomet.com
|
|