Experience with polymer processing, biocompatibility assessment, or sterilization compatibility (e ... The anticipated wage for this position is $58,000 - $123,200 Full-time equivalent employees also ...
Experience with polymer processing, biocompatibility assessment, or sterilization compatibility (e ... The anticipated wage for this position is $58,000 - $123,200 Full-time equivalent employees also ...
Experience with polymer processing, biocompatibility assessment, or sterilization compatibility (e ... The anticipated wage for this position is $58,000 - $123,200 Full-time equivalent employees also ...
Experience with polymer processing, biocompatibility assessment, or sterilization compatibility (e ... The anticipated wage for this position is $58,000 - $123,200 Full-time equivalent employees also ...
Staff Mechanical Engineer, Consumables
Pleasanton, CA · On-site
$179K - $242K/yr
... or biocompatibility failures and implementing permanent corrective actions. 4. Leadership ... Below is the base pay range for this full-time position. The actual base pay will depend on several ...
Staff Mechanical Engineer, Consumables
Pleasanton, CA · On-site
$179K - $242K/yr
... or biocompatibility failures and implementing permanent corrective actions. 4. Leadership ... Below is the base pay range for this full-time position. The actual base pay will depend on several ...
Development Engineer |Johnson & Johnson MedTech| Orthopaedics| R&D This is a permanent, full-time ... biocompatibility, risk management, and verification & validation activities. Other typical ...
Development Engineer |Johnson & Johnson MedTech| Orthopaedics| R&D This is a permanent, full-time ... biocompatibility, risk management, and verification & validation activities. Other typical ...
Full Time Biocompatibility information
See salary details
$41K - $56.7K
6% of jobs
$56.7K - $72.5K
9% of jobs
$82.4K is the 25th percentile. Wages below this are outliers.
$72.5K - $88.2K
16% of jobs
The median wage is $103.1K / yr.
$88.2K - $103.9K
20% of jobs
$103.9K - $119.6K
15% of jobs
$129.9K is the 75th percentile. Wages above this are outliers.
$119.6K - $135.4K
14% of jobs
$135.4K - $151.1K
7% of jobs
$151.1K - $166.8K
3% of jobs
$166.8K - $182.5K
1% of jobs
$182.5K - $198.3K
2% of jobs
$198.3K - $214K
6% of jobs
$41K
$115.4K
$214K
How much do full time biocompatibility jobs pay per year?
What is the difference between Full Time Biocompatibility vs Full Time Regulatory Affairs Specialist?
| Aspect | Full Time Biocompatibility | Full Time Regulatory Affairs Specialist |
|---|---|---|
| Required Credentials | Biocompatibility certifications, scientific degrees | Regulatory certifications, science or law degrees |
| Work Environment | Laboratories, manufacturing plants | Regulatory agencies, corporate offices |
| Industry Usage | Medical devices, implants | Medical devices, pharmaceuticals |
| Common Search Intent | Biocompatibility testing, safety assessment | Regulatory compliance, submissions |
Full Time Biocompatibility roles focus on testing and assessing the safety of medical materials, often requiring scientific certifications and laboratory work. In contrast, Full Time Regulatory Affairs Specialists handle compliance documentation and submissions to regulatory bodies, working more in office settings. Both roles are essential in the medical device industry but serve different functions related to product safety and approval processes.
What cities are hiring for Full Time Biocompatibility jobs?
Cities with the most Full Time Biocompatibility job openings:
What are the most commonly searched types of Biocompatibility jobs?
The most popular types of Biocompatibility jobs are:
What job categories do people searching Full Time Biocompatibility jobs look for?
The top searched job categories for Full Time Biocompatibility jobs are:

Full-time
Medical, Dental, Vision, Life, Retirement, PTO
Posted 9 days ago
Eli Lilly and Company rating
8.8
Based on 63 frontline employees who took The Breakroom Quiz
11th of 86 rated pharmaceutical
Job description
At Lilly, the work is demanding because patients are waiting. We unite caring with discovery to help make life better for people around the world, knowing that every decision, every detail, and every day matters. Headquartered in Indianapolis, Indiana, our over 50,000 employees around the globe take on complex challenges to discover and deliver life-changing medicines, strengthen how health is understood and managed, and support the communities we serve. This is hard, urgent, selfless work-but it's work worth doing. If you're driven by purpose and ready to bring your best to work that truly matters for patients, we invite you to join us.
Position Brand Description:
Provides research and technical support for materials and polymer science activities within the Technical Services/Manufacturing Sciences (TS/MS) organization, contributing to the characterization, evaluation, and qualification of materials used across Lilly's pharmaceutical manufacturing platforms.
Key Objectives/Deliverables:
- Conduct independent and collaborative research on materials and/or polymer science relevant to pharmaceutical manufacturing, container closure systems, or drug delivery devices.
- Design, execute, and interpret experiments to characterize material properties (mechanical, chemical, thermal, and surface) and structure-property relationships.
- Build and apply knowledge of materials used in Lilly's parenteral and/or device platforms, including material composition, specifications, and compatibility considerations.
- Investigate material performance, degradation mechanisms, and failure modes; support root cause analyses for material-related issues.
- Collaborate with TS/MS, R&D, and quality scientists to design and execute studies (e.g., extractables/leachable, product compatibility, sterilization compatibility) relevant to pharmaceutical materials.
- Integrate research findings into practical specifications, control strategies, and technical reports.
- Author high-quality technical reports, protocols, and scientific documentation.
- Stay current with emerging materials science research, industry trends, and regulatory expectations relevant to pharmaceutical materials.
- Present research findings to internal stakeholders and, where appropriate, contribute to peer-reviewed publications, patents, or scientific conferences.
- Mentor lab associates and/or students to enhance their technical capabilities, as opportunities arise.
- Ability to work well independently and collaboratively within global, cross-functional teams.
Basic Requirements:
- Ph.D. in Materials Engineering, Biomedical Engineering, Medical Engineering, or a closely related field.
- Demonstrated research experience in materials science and/or polymer science (e.g., through doctoral research).
- Strong understanding of material characterization techniques and structure-property relationships.
- Requires a record of publication in peer-reviewed journals and presentations/posters at scientific conferences.
Qualified applicants must be authorized to work in the United States on a full-time basis. Lilly will not provide support for or sponsor work authorization or visas for this role, including but not limited to F-1 CPT, F-1 OPT, F-1 STEM OPT, J-1, H-1B, TN, O-1, E-3, H-1B1, or L-1.
Additional Preferences:
- Experience with pharmaceutical materials, container closure systems, or drug delivery devices is a plus.
- Familiarity with GMP-regulated environments and regulatory considerations for pharmaceutical or medical device materials.
- Experience with polymer processing, biocompatibility assessment, or sterilization compatibility (e.g., gamma, e-beam, EtO).
- Ability to work well independently and remotely, as well as in global and multicultural teams.
- Strong problem-solving, analytical, and technical writing/communication skills.
- Ability to design, execute, and critically interpret scientific experiments.
Education Requirements:
Ph.D. in Materials Engineering, Biomedical Engineering, Medical Engineering, or a related scientific/engineering field.
Other Information:
- This Post-Doctoral Scientist position is not permanent. It is for a fixed duration (typically two years, with potential to extend up to a maximum of four years).
Lilly is dedicated to helping individuals with disabilities to actively engage in the workforce, ensuring equal opportunities when vying for positions. If you require accommodation to submit a resume for a position at Lilly, please complete the accommodation request form (https://careers.lilly.com/us/en/workplace-accommodation) for further assistance. Please note this is for individuals to request an accommodation as part of the application process and any other correspondence will not receive a response.
Lilly is proud to be an EEO Employer and does not discriminate on the basis of age, race, color, religion, gender identity, sex, gender expression, sexual orientation, genetic information, ancestry, national origin, protected veteran status, disability, or any other legally protected status.
Our employee resource groups (ERGs) offer strong support networks for their members and are open to all employees. Our current groups include: Africa, Middle East, Central Asia (AMECA), Black Employees at Lilly (BE@Lilly), Chinese Culture Network (CCN), EnAble, Evolve, Lilly Indian Network (LIN), Organization of Latinx at Lilly (OLA), Pride (LGBTQ+ Allies), Veterans Leadership Network (VLN) and Women's Initiative for Leading at Lilly (WILL).
Actual compensation will depend on a candidate's education, experience, skills, and geographic location. The anticipated wage for this position is
$58,000 - $123,200Full-time equivalent employees also will be eligible for a company bonus (depending, in part, on company and individual performance). In addition, Lilly offers a comprehensive benefit program to eligible employees, including eligibility to participate in a company-sponsored 401(k); pension; vacation benefits; eligibility for medical, dental, vision and prescription drug benefits; flexible benefits (e.g., healthcare and/or dependent day care flexible spending accounts); life insurance and death benefits; certain time off and leave of absence benefits; and well-being benefits (e.g., employee assistance program, fitness benefits, and employee clubs and activities).Lilly reserves the right to amend, modify, or terminate its compensation and benefit programs in its sole discretion and Lilly's compensation practices and guidelines will apply regarding the details of any promotion or transfer of Lilly employees.
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About Eli Lilly
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Eli Lilly, based in Indianapolis, IN, US, is one of the pioneers in the pharmaceutical industry with a rich history dating back to 1876. This global pharmaceutical company focuses on discovering, developing, manufacturing and selling pharmaceutical products in approximately 120 countries. The company's product categories include endocrinology, oncology, cardiovascular, neuroscience, and immunology. Having invested over $9 billion in research and development in the past decade, Eli Lilly is also committed to creating high-quality medicines that meet real needs. As a recipient of several awards and recognitions, Eli Lilly is known for its focus on life-saving research and drug development. Their mission is to make medicines that help people live longer, healthier, and more active lives.
Industry
Pharmaceutical product wholesalers
Company size
10,000+ Employees
Headquarters location
Indianapolis, IN, US
Year founded
1876