Associate Scientist I

About the role

Diasorin is a global leader in immunodiagnostic and molecular diagnostic solutions. As the Diagnostics Specialist, you will participate in the company's day-to-day research activities, including designing, executing, and interpreting scientific experiments and developing assays based on Luminex's technology platform and chemistries.

Responsibilities

• Day-to-day “hands on” work in the laboratory including generating, recording, and analyzing experimental data and maintaining laboratory notebooks.
• Occasionally, assemble and present data to departmental, project, and cross-site teams.
• Contribute to writing protocols and reports relating to feasibility, verification, and validation of molecular tests under quality system requirements.
• Interface across the organization and work closely with other functional groups such as Clinical Affairs, Design Transfer, Manufacturing, and Quality Control regarding priorities and timetables for deliverables.
• Aid in intellectual property development.
• Troubleshoot technical difficulties, as required.
• Comply with the company quality policies and operating procedures.
• Participate in the maintenance of general laboratory organization.
• Other duties as assigned.

Qualifications

• Associate's Degree Community College 2-year diploma (technical) in biochemistry, biology, molecular biology, or a related scientific field combined with at least 2 years' laboratory work experience in molecular biology or the biotechnology industry required.
• Bachelor's Degree Bachelor degree in biological/chemical or related scientific disciplines with no relevant experience/training preferred.
• 1+ Years Expertise in a variety of molecular and biochemical laboratory procedures required.
• 1+ Years Knowledge of routine laboratory methods such as PCR, data analyses, specimen handling and processing, and experimental documentation required.
• 1+ Years Working knowledge or experience with ISO 13485:2016 standards and FDA regulations preferred.
• 1+ Years Prior medical device industry experience preferred.

Training and Skills

• Excellent oral and written communication skills.
• Ability to handle the pressure of meeting tight deadlines.
• Excellent interpersonal skills with proven ability to work both in a team-oriented environment and independently.
• Knowledge of Design Control requirements as defined by the FDA Quality System guidelines.
• Mathematics and statistical aptitude.
• Data analysis and technical writing aptitude.
• Proficient in Microsoft Word, Excel, and PowerPoint programs.
• Highly organized with proven time management and prioritization skills.
• Ability to work independently and with minimal supervision.

Benefits

• Comprehensive health benefits
• Retirement and financial wellbeing
• Time off programs
• Wellbeing support and perks
• Annual incentive program

Pay

Details of pay are confidential and not disclosed publicly.

Schedule

Details of schedule are confidential and not disclosed publicly.