Scientist Biocompatibility

Johnson & Johnson•West Chester, MA

21h•Onsite

About The Position

The Scientist Biocompatibility functions as a key team member by energetically supporting the goals of Depuy Synthes Toxicology & Biocompatibility. The Scientist collaborates with associates of diverse technical backgrounds and efficiently executes the biological safety evaluation of medical device products as per internal procedures and global standards and regulations. This person is responsible for planning and execution of in vitro and in vivo biocompatibility evaluations and ensures that products meet the requirements of biological safety according to relevant standards and regulations.

Requirements

Bachelor’s or master’s degree in biology, chemistry, toxicology, microbiology, biomedical engineering, or a related scientific discipline with a minimum of 2 years of industrial experience in biocompatibility evaluation, or PhD with at least 1 year of industrial experience in biocompatibility evaluation
A minimum 1-2 years of experience in biocompatibility assessment and evaluation in a medical device, pharmaceutical, and/or consumer product company or similar combination of professional training and multi-year experience in the industry.
Experience working in a regulated environment of medical device safety and supporting product submission and audit is required
Knowledge of toxicology & biocompatibility assessment of medical devices, coordination, and interpretation of biocompatibility and chemistry studies per relevant guidelines and requirements

Nice To Haves

support for worldwide market registration is preferred
Understanding of manufacturing processes of medical devices is preferred
Biofabrication
Biological Sciences
Biomaterials
Biostatistics
Communication
Data Savvy
Detail-Oriented
Execution Focus
Feasibility Studies
Preclinical Research
Quality Standards
Quality Validation
Report Writing
Research and Development
Researching
SAP Product Lifecycle Management
Technologically Savvy

Responsibilities

Evaluates DePuy Synthes medical device products and materials for biological safety per international medical device regulations and standards, GLP (Good Laboratory Practice) guidelines and internal procedures.
Designs, initiates, coordinates, and interprets laboratory investigations for biocompatibility and toxicology studies for MD materials and products.
Applies technical expertise to solve biocompatibility problems related to the ISO 10993 standards and regulatory authority requirements for product safety.
Liaises with internal and cross-functional team members to review existing product documentation and coordinates, together with more senior staff, biocompatibility test strategies to ensure appropriate planning and execution of required testing and completion of relevant deliverables.
Reviews, interprets, and summarizes testing data and ensures appropriate documentation and coordination of central documentation procedures required for risk assessment report completion.
Interacts closely with and provides technical guidance and expertise to internal stakeholders (e.g., R&D, Clinical Affairs, Regulatory Affairs, Manufacturing, Quality Engineering, and Supplier Management)
Can support regulatory/notified body requests as part of Audits and File/Product submissions/Reviews in applicable markets.
Maintains effective communication of business-related issues or opportunities to next management level and if necessary, SMEs, via proper communication methods and/or tools.
Identifies and evaluates potential risks and drives resolution with team members, peers, PMO and management.
Participates in continuous improvement activities and actively participates in shaping processes and procedures
Responsible for communicating business related issues or opportunities to next management level
Responsible for following all Company guidelines related to Health, Safety and Environmental practices as applicable.
For those who supervise or manage a staff, responsible for ensuring that subordinates follow all Company guidelines related to Health, Safety and Environmental practices and that all resources needed to do so are available and in good condition, if applicable
Responsible for ensuring personal and Company compliance with all Federal, State, local and Company regulations, policies, and procedures
Performs other duties assigned as needed

Benefits

Consolidated retirement plan (pension)
Savings plan (401(k))
Long-term incentive program
Vacation –120 hours per calendar year
Sick time - 40 hours per calendar year; for employees who reside in the State of Colorado –48 hours per calendar year; for employees who reside in the State of Washington –56 hours per calendar year
Holiday pay, including Floating Holidays –13 days per calendar year
Work, Personal and Family Time - up to 40 hours per calendar year
Parental Leave – 480 hours within one year of the birth/adoption/foster care of a child
Bereavement Leave – 240 hours for an immediate family member: 40 hours for an extended family member per calendar year
Caregiver Leave – 80 hours in a 52-week rolling period
Volunteer Leave – 32 hours per calendar year
Military Spouse Time-Off – 80 hours per calendar year