About the Company
Quest Diagnostics is the world’s leading provider of diagnostic information services. We provide insights that help people live healthier lives, offering a broad portfolio of innovative laboratory services that go beyond testing to provide actionable insights. With a relentless focus on quality and innovation, we are committed to being a partner in healthcare across the entire patient journey, from wellness and prevention to chronic disease management and clinical trials support.
Job Description
We are seeking a highly skilled Pharmaceutical Lab Tech with a specialized focus on clinical trials to join our dynamic team in Fullerton, CA. In this crucial role, you will be responsible for performing a variety of complex laboratory procedures, adhering strictly to established protocols for clinical trial samples. Your expertise will directly contribute to the accurate and timely processing of samples, ensuring the integrity and reliability of data essential for clinical research and drug development. This position requires meticulous attention to detail, strong organizational skills, and a comprehensive understanding of Good Laboratory Practices (GLP) and Good Clinical Practice (GCP) guidelines.
Key Responsibilities
- Perform complex laboratory procedures and analyses on clinical trial samples, including but not limited to immunoassay, molecular diagnostics, and general chemistry.
- Operate, maintain, and calibrate various laboratory equipment, ensuring optimal performance and troubleshooting issues as needed.
- Strictly adhere to clinical trial protocols, Standard Operating Procedures (SOPs), and regulatory guidelines (GLP, GCP).
- Document all experimental data accurately, thoroughly, and in a timely manner, maintaining detailed records in laboratory information systems (LIS) and other relevant databases.
- Prepare reagents, media, and solutions according to precise specifications.
- Assist in the development and validation of new assays and methodologies relevant to clinical trials.
- Manage inventory of samples, reagents, and supplies, ensuring proper storage and tracking.
- Participate in quality control and quality assurance activities, contributing to continuous improvement efforts.
- Communicate effectively with internal teams, including clinical project managers, scientists, and other lab personnel, regarding sample status and results.
- Ensure a clean, organized, and safe working environment, complying with all safety regulations.
Required Skills
- Minimum of 3 years of experience in a clinical or pharmaceutical laboratory setting, with a significant focus on clinical trial sample processing.
- Proficiency in performing a variety of laboratory techniques (e.g., ELISA, PCR, chromatography).
- Thorough understanding of GLP and GCP regulations.
- Experience with Laboratory Information Systems (LIS) and electronic data management.
- Excellent aseptic technique and attention to detail.
- Strong problem-solving and analytical abilities.
- Ability to work independently and as part of a team in a fast-paced environment.
- Strong written and verbal communication skills.
- Bachelor's degree in Medical Technology, Biology, Chemistry, or a related scientific field.
Preferred Qualifications
- ASCP certification or equivalent.
- Master's degree in a relevant scientific discipline.
- Experience with automated laboratory systems.
- Familiarity with specific therapeutic areas in clinical research (e.g., oncology, infectious diseases).
Perks & Benefits
- Comprehensive health, dental, and vision insurance plans.
- 401(k) retirement plan with company match.
- Paid time off (PTO) and company holidays.
- Tuition reimbursement and professional development opportunities.
- Life insurance and disability benefits.
- Employee assistance program (EAP).
- Opportunities for career growth within a leading global diagnostic company.
How to Apply
If you are interested in this position, please click the "Apply Now" button below. To ensure your application is properly considered, please prepare the following:
- An up-to-date Resume or CV
- A brief cover letter summarizing your experience and motivation
Applications are reviewed on a rolling basis. Only shortlisted candidates will be contacted for an interview.
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