Technician, R&D II

AbbVie Inc; Irvine (CA); On-site; USD 50,000 - 90,000; Full time

Job summary

A forward-thinking company is seeking a dedicated individual to join their Local Delivery Safety Translational Sciences team. This role involves providing technical support for in vivo studies, ensuring compliance with regulations, and generating high-quality data. The ideal candidate will have a strong background in pre-clinical toxicology and pharmacokinetics, along with excellent problem-solving and communication skills. Join a team that values innovation and integrity, and contribute to impactful research that addresses critical health challenges.

Benefits

Paid time off

Medical insurance

Dental insurance

Vision insurance

401(k) plan

Short-term incentive programs

Qualifications

• 5+ years technical work experience in specialty areas or relevant degree with 2+ years experience.
• Understanding of dosing, observational techniques, and study management.

Responsibilities

• Provide technical support for IVS studies and assist Study Director with protocol setup.
• Demonstrate proficiency in in vivo procedures and train personnel on experimental techniques.

Skills

Pre-clinical toxicology

Pharmacokinetics

Data collection

Problem-solving

Communication skills

Education

High School/GED

A.S., B.S. or B.A in biology

Tools

Microsoft Office

Electronic data capture systems

Job description

Company Description

AbbVie's mission is to discover and deliver innovative medicines and solutions that solve serious health issues today and address the medical challenges of tomorrow. We strive to have a remarkable impact on people's lives across several key therapeutic areas – immunology, oncology, neuroscience, and eye care – and products and services in our Allergan Aesthetics portfolio. For more information about AbbVie, please visit us atwww.abbvie.com. Follow @abbvie onX,Facebook,Instagram,YouTube,LinkedInandTik Tok.

Job Description

Under limited supervision, this position in the Local Delivery Safety Translational Sciences (LDSTS) department is responsible for the technical support of in vivo studies in accordance with study protocols, Good Laboratory Practice (GLP) regulations, Standard Operating Procedures (SOPs), IACUC and departmental guidelines. The position requires basic understanding of pre-clinical toxicology and pharmacokinetic study conduct in addition to knowledge of regulatory and animal welfare requirements. In collaboration with the Study Director and other relevant personnel, the incumbent will manage all technical aspects of study conduct and will generate high quality data for assigned studies.

The incumbent will also support implementation of process improvements with respect to study execution and departmental capabilities and when qualified will be responsible for training technical staff on new in vivo procedures.

Responsibilities:

• Provides technical support for IVS studies with minimal supervision. Acts as Study Coordinator for assigned studies and assists Study Director with protocol setup. Prepares study calendar and notebook, generates data sheets, ensures study supplies are available, prepares test article formulation and handling records.
• Demonstrates technical proficiency in general in vivo procedures such as dosing, sample collection, and clinical observations of rodent and non-rodent species. Proficient in the use of department automated data collection. Participates in training personnel in various experimental procedures and proper equipment operation.
• Provides assistance for short or long-term assignments in support of department functions that may include administrative or clerical duties, report writing support, inventory, equipment maintenance, etc. Maintains up-to-date knowledge and skill in general animal dosing and sample collection procedures. Learns new techniques and concepts by reading journals, attending meetings and lectures and participating in available training and certification programs.

Qualifications

• High School/GED is required AND at least 5 years prior relevant technical workexperience in area(s) of specialty OR A.S., B.S. or B.A in biology, biochemistry, animal science or related field with 2 or more years of relevant work experience
• Experience with the conduct of pre-clinical toxicology and/or pharmacokinetic studies is preferred

Essential Skills and Abilities

• Understanding of basic pre-clinical study-related functions including dosing, observational and sampling techniques in relevant laboratory animal species, and study set up and management.
• Ability to lift at least 40 pounds, stand for extended periods, perform visual examinations and manually manipulate equipment.
• Strong interpersonal, organizational, problem-solving, and verbal and written communication skills
• Demonstrated ability to work well in a team or matrix environment
• Proficiency with computer software including Microsoft Office and electronic data capture systems.

Additional Information

Applicable only to applicants applying to a position in any location with pay disclosure requirements under state or local law:

• The compensation range described below is the range of possible base pay compensation that the Company believes ingood faith it will pay for this role at the time of this posting based on the job grade for this position. Individualcompensation paid within this range will depend on many factors including geographic location, and we may ultimatelypay more or less than the posted range. This range may be modified in the future.

• We offer a comprehensive package of benefits including paid time off (vacation, holidays, sick), medical/dental/visioninsurance and 401(k) to eligible employees.

• This job is eligible to participate in our short-term incentive programs.

Note: No amount of payis considered to bewages or compensation until such amount is earned, vested, and determinable.The amount and availability of any bonus, commission, incentive, benefits, or any other form of compensation and benefitsthat are allocable to a particular employee remains in the Company's sole and absolute discretion unless and until paid andmay be modified at the Company’s sole and absolute discretion, consistent with applicable law.

AbbVie is an equal opportunity employer and is committed to operating with integrity, driving innovation, transforming lives and serving our community. Equal Opportunity Employer/Veterans/Disabled.

US & Puerto Rico only - to learn more, visithttps://www.abbvie.com/join-us/equal-employment-opportunity-employer.html

US & Puerto Rico applicants seeking a reasonable accommodation, click here to learn more:

https://www.abbvie.com/join-us/reasonable-accommodations.html