Abbott is a global healthcare leader that helps people live more fully at all stages of life. Our portfolio of life-changing technologies spans the spectrum of healthcare, with leading businesses and products in diagnostics, medical devices, nutritionals and branded generic medicines. Our 114,000 colleagues serve people in more than 160 countries.
Our rapid diagnostics solutions are helping address some of the world's greatest healthcare challenges.
Working at Abbott At Abbott, you can do work that matters, grow, and learn, care for yourself and family, be your true self and live a full life. You'll also have access to:
Career development with an international company where you can grow the career you dream of.
Free medical coverage for employees via the Health Investment Plan (HIP) PPO.
An excellent retirement savings plan with high employer contribution.
Tuition reimbursement, the Freedom 2 Save student debt program and FreeU education benefit - an affordable and convenient path to getting a bachelor's degree.
A company recognized as a great place to work in dozens of countries around the world.
The Opportunity The position of Scientific Affairs Director is within our Toxicology business unit. The person can work onsite in either our Lake Forest, IL or Pomona, CA locations. This role will provide Toxicology Business Unit Strategic direction through leading interactions with Toxicology Key Opinion Leaders, Government agencies, Professional Societies and potential strategic partnerships that will advance Business Unit strategic Plan.
This role is to provide Scientific insight throughout Abbott Toxicology, engaging with internal and external entities, collating, and summarizing data, presenting at professional conferences and assuring with technical projects. This role will also be responsible for overseeing the development and implementation of analytical procedures; presenting data at professional conferences; publishing new method and assay data; assisting with technical marketing projects; collation of data from external research projects. This is not available for hybrid or remote work.
What You'll Work On Ensure that new products meet the needs of a rapidly changing drug testing field.
Work closely with the biologics group for appropriate selection of antibodies.
Provide scientific rationale for cut-offs and cross-reactants as necessary.
Ensure research group maintains leadership in the field of analytical technologies related to immunoassays.
Work with Regulatory Assurance group and other departments to assist in development, documentation and registrations (e.g. IVDR and FGDA 510K) for novel technologies and products.
Participate in Design Review and other meetings as required for new product development and launch.
Assist in product marketing by providing technical information, presentations, and review.
Assist in resolving customer complaints if necessary.
Work across the business units to provide technical leadership in product development.
Represent the company in a professional capacity including, but not limited to, at scientific conferences, on advisory boards, in relevant working groups and during government communications.
Oversee development and implementation of analytical procedures which support company products.
Collaborate with external researchers on grant submissions.
Organize or assist in promoting relevant workshops, webinars, and presentations.
Develop projects with law enforcement to address issues surrounding DUID and traffic safety.
Remain active in relevant professional societies.
Provide technical expertise to legislators and the public regarding new matrix analysis for drug testing in drivers.
Understand and be aware of the quality consequences which may occur from the improper performance of their specific job; has awareness of device defects that may occur in their area of responsibility, including product design, verification and validation, manufacturing and testing activities.
Exhibit professional behavior with both internal/external business associates that reflects positively on the company and is consistent with the company's policies and practices; build productive internal/external working relationships.
Perform duties in compliance with established business policies.
Other duties as assigned, according to the changing needs of the business.
Required Qualifications PhD in field of analytical chemistry, forensic toxicology, Clinical Chemistry, Clinical Toxicology, or Immunochemistry.
Board certification in clinical chemistry or related subject.
Travel required 25-30%.
Minimum of 10-12 years laboratory experience.
Working knowledge of immunoassay and mass spectrometry.
Excellent writing and communication skills for preparation of publications, reports, and presentations.
History of diverse, published, peer-reviewed scientific papers.
Effective organizational capabilities.
Strong people skills and ability to work as a team player.
Knowledge of computers and software programs including Word, Excel, Power Point, and document management programs.
Ability to work in a highly matrixed, cross-functional organization.
Preferred Qualifications Analysis of biological specimens for drugs in a high throughput laboratory environment.
Data review for immunoassay screening and mass spectrometry results.
Experience leading and supervising scientific staff.
Tox lab and/or production service lab management experience.
Follow your career aspirations to Abbott for diverse opportunities with a company that can help you build your future and live your best life. Abbott is an Equal Opportunity Employer, committed to employee diversity.
The base pay for this position is $143,300.00 – $286,700.00. In specific locations, the pay range may vary from the range posted.
#J-18808-Ljbffr
