Title: Technical Support Scientist II
Location: Pomona, California
Duration: 11 Month with possibility of extension or conversion
Shift: 7AM - 3:30PM
100% On-Site
Job Summary:
Provide technical support within the Drugs of Abuse manufacturing facility, supporting product improvements, change control processes, investigations, technical issue resolution, and verification/validation studies for new or modified materials. Responsible for data analysis, technical documentation, report generation, and collaboration with cross-functional teams.
Job Responsibilities:
- Perform product testing, data analysis, and prepare technical reports.
- Conduct verification and validation studies, protocols, and reports.
- Investigate technical issues, perform root cause investigations, and recommend solutions.
- Develop and improve methods, processes, and testing procedures.
- Review, edit, and maintain controlled documentation in electronic document management systems.
- Compile and analyze data using Microsoft Excel and Word.
- Maintain accurate laboratory records and documentation.
- Evaluate and recommend improved testing methods.
- Support change control processes and quality incident management.
- Participate in project teams and departmental meetings.
- Ensure compliance with business policies, QSR, ISO, and FDA requirements.
- Guide less experienced staff and assist with problem solving.
Qualifications - Must Have:
- BA or BS in Chemistry or Biological Sciences.
- Minimum 3 years of experience in a related field.
- Strong verbal and written communication skills.
- Good technical writing skills.
- Ability to follow detailed instructions and maintain accurate records.
- Experience conducting experiments and accurately summarizing results.
- Demonstrated problem-solving and troubleshooting skills.
- Knowledge of laboratory equipment and operations.
- Ability to work independently and in a team environment.
- Proficiency with Microsoft Excel, Word, and electronic document management systems.
Qualifications - Preferred:
- Knowledge of MS Office and manufacturing systems.
- Ability to functionally direct junior research staff.
- Adaptable and willing to take on multiple responsibilities.
- Independent, collaborative self-starter with strong decision-making skills.
- Process-oriented, analytical, meticulous, and highly organized.
- Ability to analyze data and implement solutions effectively.
- Proven ability to work effectively within a team environment while meeting individual responsibilities and objectives.
Consultants Eligible Benefits Upon Waiting Period:
- Medical and Prescription Drug Plans
- Dental Plan
- Vision Plan
- Health Savings Account (for High-Deductible Health Plans)
- Flexible Spending Accounts (Health, Limited Purpose, Dependent Care, Commuter Parking and Commuter Transit)
- Supplemental Life Insurance
- Short Term Disability (coverage varies by state)
- Long Term Disability
- Critical Illness, Hospital coverage, Accident Insurance
- MetLife Legal, MetLife ID Fraud, and MetLife Pet Insurance
- 401(k)
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, nutritional and branded generic medicines.
Working together, Abbott and Talent Solutions partner to deliver top talent for contingent roles at Abbott, building better and healthier lives. Abbott believes all employees are essential to creating life-changing breakthroughs, performing key duties to create life-changing breakthroughs.