The position of Technical Support Scientist is within our Toxicology Business Unit located in Pomona, California. This position will provide technical support functions within our Drugs of Abuse manufacturing facility. The position will primarily be focused on participating in moderate complexity, short-to long-duration projects, product improvements, change control processes, investigations and resolving technical issues in coordination with another department. This position will also conduct verification or validation study for new or modified material and generate reports.
What You’ll Work On
Has a good knowledge for each process of products testing
Investigates and may create and develop new methods and processes for project advancement with guidance from more experienced colleague
Familiarity with all aspects of product
Conducts experiments of moderate complexity projects, seek advice when needed from more experienced colleagues for more complicated technical and design challenges
Possesses and applies knowledge of principles, practices, and procedures of particular field of specialization to the completion of moderately complex assignments.
Works on problems of moderate and diverse scope in which analysis of data requires evaluation of identifiable factors. Proposes potential solutions to more advance problems.
May plan and work on projects of smaller complexity under limited supervision.
Perform customer complaint investigation and write report
Work independently and effectively. Cooperatively work with others in all matter of the organization
Be able to prioritize and handle multiple tasks and responsibilities, attention to details
Moderate computer skill and moderate knowledge of MS Excel and MS Word
Use Agile to issue quality incidence; perform root cause investigation and write investigation report
No formal supervisor duties, but may direct less experienced staff in their day-to-day work and assist in problem solving
Test product, compile data, perform data analysis and prepare reports for product improvements and investigations
Maintain records of laboratory activities in a professional, accurate manner
Report progress and results to manager on a regular basis
Evaluate and recommend improved testing methods
Able to solve process-related questions/problems
With minimal guidance can write verification and validation protocols and reports, order materials needed to complete procedures, write technical reports
Actively participate in departmental meetings as well as representing Technical Support on project teams
Establish new and modify existing documentation in a manner which will achieve accuracy and avoid errors and potential production issues
Review, edit and process changes to controlled documentation such as procedures, forms, etc., in an electronic document management system
Use Microsoft Excel and Word to compile test data, perform appropriate analyses and write technical report/documentation such as deviation reports, validation protocol and trend analyses
Understands and is 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
Responsible for exhibiting 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
Carries out duties in compliance with established business policies
Knowledgeable of federal and other regulations, e.g. QSR’s, ISO and FDA
Other duties as assigned, according to the changing needs of the business
Required Qualifications
BA or BS in Chemistry or Biological Sciences
Minimum 3 years’ experience in related field
Strong verbal and written communication skills
Good technical writing skills
Ability to follow detailed instructions, maintains accurate records and notes, and carries out assignments in a thorough, conscientious fashion while adhering to safe laboratory practices
Able to carry out experiments following established guidelines and summarize results accurately.
Demonstrate problem-solving and troubleshooting skills
Knowledge of a variety of lab equipment and their operation
Able to functionally direct junior research staff
Preferred Qualifications
Knowledge and ability to use MS Office and other manufacturing systems
Adaptable and willing to take on multiple new tasks and responsibilities
Independent collaborative self-starter with the ability to make appropriate quality-related decisions in real time
Process orientated, Logical, analytical, meticulous, highly organized and able to analyze data & implement solutions
Proven ability to work effectively within a team environment while satisfying individual responsibilities and objectives
Apply Now
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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.
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- The base pay for this position is
- $81,500.00 – $141,300.00
- In specific locations, the pay range may vary from the range posted.
JOB FAMILY
Research and Discovery
DIVISION
TOX ARDx Toxicology
LOCATION
United States > Pomona : 829 Towne Center Drive
ADDITIONAL LOCATIONS
WORK SHIFT
Standard
TRAVEL
No
MEDICAL SURVEILLANCE
Not Applicable
SIGNIFICANT WORK ACTIVITIES
Continuous sitting for prolonged periods (more than 2 consecutive hours in an 8 hour day), Continuous standing for prolonged periods (more than 2 consecutive hours in an 8 hour day), Keyboard use (greater or equal to 50% of the workday)
Abbott is an Equal Opportunity Employer of Minorities/Women/Individuals with Disabilities/Protected Veterans.
EEO is the Law link - English: http://webstorage.abbott.com/common/External/EEO_English.pdf
EEO is the Law link - Espanol: http://webstorage.abbott.com/common/External/EEO_Spanish.pdf
