Technical Support Scientist

Abbott; United States; On-site; USD 81,500 - 141,300; Full time

Job summary

Abbott Rapid Diagnostics, part of Abbott Diagnostics, seeks a Technical Support Scientist for the Drugs of Abuse manufacturing facility in Pomona, California. You will support projects, run moderate-complexity experiments, and prepare reports.

You will collaborate with teams, maintain records, ensure compliance with FDA/QSR/ISO, and use Excel and Word to document findings. The role offers growth in a global health care leader.

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 fashion while adhering to safe laboratory practices.
• Able to carry out experiments following established guidelines and summarize results accurately.
• Knowledge of a variety of lab equipment and their operation.
• Able to functionally direct junior research staff.

Responsibilities

• Provide technical support within the Drugs of Abuse manufacturing facility.
• Conduct moderate-complexity experiments and participate in project work.
• Prepare reports and documentation for investigations and product improvements.
• Perform root cause analysis and write investigation reports.
• Maintain accurate records of laboratory activities and communicate progress to management.

Skills

Verbal and written communication

Technical writing

MS Excel

MS Word

Attention to detail

Education

BA/BS in Chemistry or Biological Sciences

Tools

MS Office

Laboratory equipment knowledge

Job description

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 115,000 colleagues serve people in more than 160 countries.

JOB DESCRIPTION:

_ Technical Support Scientist _

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.

• Employees can qualify for free medical coverage in our Health Investment Plan (HIP) PPO medical plan in the next calendar year.

• 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 and named one of the most admired companies in the world by Fortune.

• A company that is recognized as one of the best big companies to work for as well as a best place to work for diversity, working mothers, female executives, and scientists.

The Opportunity

Abbott Rapid Diagnostics is part of Abbott’s Diagnostics family of businesses, bringing together exceptional teams of experts and industry leading technologies to support diagnostic testing which provides important information for treatment and management of diseases and other conditions.

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, seeks 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 that 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.

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

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 - Español: http://webstorage.abbott.com/common/External/EEO_Spanish.pdf