Job Description

Our direct client in the Medical Device Industry is seeking a motivated and detail-oriented individual to join their Biocompatibility & Toxicology team as a Laboratory Technician (part-time, 20 hours/week). This position provides a valuable opportunity to acquire knowledge and hands-on experience in in-vitro biocompatibility and toxicology testing, supporting medical device biocompatibility risk assessments. In addition to performing laboratory tasks, the ideal candidate will be involved in the creation, review, and drafting of Standard Operating Procedures (SOPs) to ensure compliance with internal company requirements and global regulations.

Qualifications:

• Minimum of a Bachelor's degree in Biology, Toxicology, or a related Life Sciences field is required.

• Candidates must have prior hands-on experience in an industrial setting involving in vitro cell work, experience in toxicological assays (viability, inflammation, irritation, sensitization, etc) is highly preferred.

• Experience with advanced in vitro models related to skin irritation and sensitization testing is desirable. Candidates with proven experience from academic laboratories will also be considered.

• Good verbal and written communication and excellent organization and time management skills.

• Basic proficiency in word processing, Excel, email applications, and knowledge of statistical analysis is required.

• A strong willingness to learn and adapt to new laboratory techniques and technologies.

• Ability to multitask effectively and work collaboratively as a team player within cross-functional teams.

Responsibilities:

• Assist in and conduct routine cell culture activities, biocompatibility laboratory testing, and accurately record and transmit data in support of ongoing biocompatibility studies.

• Collect and document data meticulously, contributing to the drafting of reports as needed.

• Provide support to the team in managing multiple tasks while effectively responding to study needs.

• Participate in the creation and review of internal Standard Operating Procedures (SOPs).

• Execute approved SOPs while ensuring compliance in all activities.

• Collaborate with experienced lab personnel to enhance understanding of laboratory practices and techniques.

•Involved in GLP archiving.

• Assist in the planning stages of test protocols, ensuring adherence to documented activities.

• Adapt swiftly to changes in protocols and acquire proficiency in new test methods.

• Aid in the acquisition, tracking, and management of samples designated for testing.

• Foster an inclusive environment through proactive self-reflection and respectful collaboration with team members.

• Complete other tasks as assigned to support the team and organizational needs.

This position presents an excellent opportunity to develop your skills, gain relevant experience, and contribute to impactful research in biocompatibility and toxicology. If you are eager to engage with the field of medical device biocompatibility evaluation, we encourage you to apply.

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