Technician, R&D II

BioSpace; Irvine (CA); On-site; USD 40,000 - 80,000; Full time

Job summary

An established industry player is seeking a dedicated Technician for R&D, focusing on in vivo studies and technical support. This role involves managing study protocols, ensuring compliance with GLP regulations, and generating high-quality data. The ideal candidate will have a strong background in pre-clinical toxicology, excellent communication skills, and the ability to work effectively in a team. Join a forward-thinking company where your contributions will play a vital role in advancing innovative medicines and solutions that significantly impact health outcomes. This is a fantastic opportunity for those passionate about scientific research and animal welfare.

Qualifications

• 5+ years of relevant technical experience or 2+ years with a degree.
• Experience with pre-clinical toxicology and pharmacokinetic studies preferred.

Responsibilities

• Provides technical support for IVS studies with minimal supervision.
• Demonstrates proficiency in in vivo procedures and trains personnel.
• Supports departmental functions including report writing and equipment maintenance.

Skills

Pre-clinical toxicology understanding

Dosing procedures

Sample collection

Strong communication skills

Organizational skills

Problem-solving skills

Ability to work in teams

Education

High School/GED

Associate's degree in biology or related field

Bachelor's degree in biology or related field

Tools

Microsoft Office

Electronic data systems

Job description

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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, along with products and services in our Allergan Aesthetics portfolio. For more information about AbbVie, please visit us at www.abbvie.com. Follow @abbvie on X, Facebook, Instagram, YouTube, LinkedIn, and TikTok.

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 role requires a basic understanding of pre-clinical toxicology and pharmacokinetic study conduct, along with knowledge of regulatory and animal welfare requirements. In collaboration with the Study Director and other personnel, the incumbent manages all technical aspects of study conduct and generates high-quality data.

The incumbent will also support process improvements related to study execution and departmental capabilities and, when qualified, will train technical staff on new in vivo procedures.

Responsibilities

1. Provides technical support for IVS studies with minimal supervision. Acts as Study Coordinator, assists with protocol setup, prepares study documentation, and ensures availability of study supplies.
2. Demonstrates proficiency in in vivo procedures such as dosing, sample collection, and clinical observations in rodent and non-rodent species. Participates in training personnel and maintains knowledge of experimental procedures.
3. Supports departmental functions, including administrative duties, report writing, inventory, and equipment maintenance. Continuously updates skills through journals, meetings, and training programs.

Qualifications

• High School/GED with at least 5 years of relevant technical experience or an Associate's, Bachelor's, or Bachelor's degree in biology, biochemistry, animal science, or a related field with at least 2 years of relevant experience.
• Experience with pre-clinical toxicology and/or pharmacokinetic studies is preferred.

Essential Skills and Abilities

• Understanding of pre-clinical study functions, dosing, sampling, and study management.
• Ability to lift at least 40 pounds, stand for extended periods, and perform visual and manual tasks.
• Strong communication, organizational, and problem-solving skills.
• Ability to work effectively in a team or matrix environment.
• Proficiency with Microsoft Office and electronic data systems.

Additional information on compensation, benefits, and equal opportunity employment policies is provided in the original description.