A-Line Staffing is now hiring Staff Scientist in Sam Diego, CA. The Staff Scientist would be working for a Fortune 500 company and has career growth potential. This would be full time / 40+ hours per week.

If you are interested in this Staff Scientist position, please contact Sawyer at sbollitier@alinestaffing.com

Staff Scientist Compensation

• The pay for this position is $57.64 per hour
• Benefits are available to full-time employees after 90 days of employment
• A 401(k) with a company match is available for full-time employees with 1 year of service on our eligibility dates

Staff Scientist Highlights

• This position is a contract assignment with potential to hire on permanently based upon attendance, performance, and business needs
• The required availability for this position is 30-40 depending on workload. San Diego Hybrid (preferred) or can be remote.

Staff Scientist Responsibilities

• -Contribute as local SME to the design, execution and interpretation of preclinical safety, biocompatibility, analytical chemistry, and toxicological evaluation strategies and programs according to relevant regulatory requirements; including review of literature and assessment of compliance. Collaborate with CPDT SMEs, BD project teams, business unit regulatory affairs staff, R&D staff and outside suppliers as required to help define product testing requirements and coordinate with the project team to provide CPDT deliverables.
• -Serve as Sponsor Representative for biocompatibility and chemistry studies and contribute to design, execution, and interpretation of preclinical, biocompatibility, chemistry and toxicological evaluation programs for medical devices within BD.
• -Support EU MDR remediation efforts, create biocompatibility evaluation reports, and conduct testing as needed to ensure compliance under the EU MDR.
• -Maintain historical databases and perform searches of historical data, as needed.

Staff Scientist Requirements

• Bachelor’s degree in toxicology or a closely related field OR minimum of 8 years of pre-clinical medical device development experience OR Master’s degree in toxicology or a closely related field and a minimum of 5 years pre-clinical medical device development experience OR PhD Degree in toxicology or a closely related field and a minimum of 2 years pre-clinical medical device development experience years relevant experience or a combination of equivalent education and relevant experience.
• Board certification in toxicology preferred (e.g., DABT, ERT)
• Experience in a GLP preclinical environment preferred.
• Working knowledge of computers (Word, Excel, Access, PowerPoint, SharePoint).
• Skills/Abilities A broad background in biology/biocompatibility, toxicology and analytical chemistry  including familiarity with recent methodologies and evaluation techniques (i.e., ISO 10993 and related guidance).
• Experience in a United States or EU medical device setting preferred.
• Ability to communicate and work effectively with national and international, internal, and external teams.
• Must be able to multitask and operate effectively within a diverse work environment. Must be team oriented and have strong interpersonal skills and customer focus while functioning independently as an SME.
• Must have excellent scientific written and verbal communication skills.
• High School Diploma or GED
• Attendance is mandatory for the first 90 days

If you think this Staff Scientist position is a good fit for you, please reach out to me - feel free to call, e-mail, or apply to this posting!

Staff Scientist Requirements

• Bachelor’s degree in toxicology or a closely related field OR minimum of 8 years of pre-clinical medical device development experience OR Master’s degree in toxicology or a closely related field and a minimum of 5 years pre-clinical medical device development experience OR PhD Degree in toxicology or a closely related field and a minimum of 2 years pre-clinical medical device development experience years relevant experience or a combination of equivalent education and relevant experience.
• Board certification in toxicology preferred (e.g., DABT, ERT)
• Experience in a GLP preclinical environment preferred.
• Working knowledge of computers (Word, Excel, Access, PowerPoint, SharePoint).
• Skills/Abilities A broad background in biology/biocompatibility, toxicology and analytical chemistry  including familiarity with recent methodologies and evaluation techniques (i.e., ISO 10993 and related guidance).
• Experience in a United States or EU medical device setting preferred.
• Ability to communicate and work effectively with national and international, internal, and external teams.
• Must be able to multitask and operate effectively within a diverse work environment. Must be team oriented and have strong interpersonal skills and customer focus while functioning independently as an SME.
• Must have excellent scientific written and verbal communication skills.
• High School Diploma or GED
• Attendance is mandatory for the first 90 days