Associate Scientist II

Job Scope

This position will be responsible for participating in the company's day-to-day Research & Development activities which include design, execution and interpretation of scientific experiments and design and development of assays based on Luminex's technology platform and chemistries. Handles scientific experiments independently with minimal supervision.

Key Duties And Responsibilities

• Day-to-day “hands on” work in the laboratory including, planning and designing of experiments, generating, recording, and analyzing experimental data and maintaining laboratory notebooks.
• Routinely, assemble and present data to departmental, project, and cross-site teams
• Significantly 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, Quality Affairs, Regulatory Affairs, Clinical Affairs, Design Transfer, Manufacturing, and Quality Control regarding priorities and timetables for deliverables
• Provide training and technical support to junior members of the team
• 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
• Performs other duties as assigned related to duties as assigned

Education, Experience, And Qualifications

• Associate's Degree Community College 2-year diploma (technical) in biochemistry, biology, molecular biology, or a related scientific field combined with at least 5 years’ laboratory work experience in molecular biology or the biotechnology industry required
• or Bachelor's Degree Bachelor degree in biological/chemical or related scientific disciplines with 2 years relevant experience/training preferred
• or Master's Degree Master’s degree in biological/chemical or related scientific disciplines with no relevant experience/training preferred
• 2+ Years Expertise in a variety of molecular and biochemical laboratory procedures required
• 2+ Years Knowledge of routine laboratory methods such as PCR, data analyses, specimen handling and processing, and experimental documentation required
• 2+ Years Working knowledge or experience with ISO 13485:2016 standards and FDA regulations preferred
• 2+ Years Prior medical device industry experience preferred
• Excellent oral and written communication skills. (High proficiency)
• Proficient in Microsoft Word, Excel, and PowerPoint programs. (High proficiency)
• Highly organized with proven time management and prioritization skills (High proficiency)
• Ability to work independently and with minimal supervision (High proficiency)
• Ability to handle the pressure of meeting tight deadlines (High proficiency)
• Excellent interpersonal skills with proven ability to work both in a team-oriented environment and independently (High proficiency)
• Knowledge of Design Control requirements as defined by the FDA Quality System guidelines (Medium proficiency)
• Data analysis and technical writing aptitude. (Medium proficiency)

What We Offer

• The hiring range for this position is $57,738 - $98,155 annually.
• Beyond base salary, Diasorin offers a competitive rewards package focused on your overall well-being. We are proud to offer a comprehensive plan of health benefits, retirement and financial wellbeing, time off programs, wellbeing support and perks.
• You may also be eligible to participate in an annual incentive program. An incentive award, if any, depends on various factors, including, individual and organizational performance.
• Diasorin is an equal opportunity employer. All qualified applicants will receive consideration for employment without regard to race, color, religion, sex, sexual orientation, gender identity, national origin, or protected veteran status, and will not be discriminated against on the basis of disability.

Additional Information

• In compliance with federal law, all persons hired will be required to verify identity and eligibility to work in the United States and Canada and to complete the required employment eligibility verification document form upon hire.
• Diasorin is committed to providing reasonable accommodations for qualified individuals with disabilities. If you are a US or Canada candidate and require assistance or accommodation during the application process, please contact the North America Talent Acquisition Team at hrtalent@diasorin.com or 1-800-328-1482 to request an accommodation.
• The above job description is intended to describe the general content, identify the essential functions, and set forth the requirements for the performance of this job. It is not to be construed as an exhaustive statement of duties, responsibilities, or requirements. Diasorin reserves the right to modify or amend this job posting as needed to comply with local laws and regulations.
• Please note that offers of employment at Diasorin may be contingent upon successful completion of a pre-employment background check and drug screen, subject to applicable laws and regulations.
• This position is not eligible for partnership with a third-party search firm vendor without expressed, written consent from the Diasorin Human Resources Department.