Molecular R&D Validation Associate

Diasorin is a global leader in diagnostic solutions, pushing the boundaries of science and technology to create cutting-edge tools that improve healthcare worldwide. With a legacy spanning over 50 years, we've earned our reputation for excellence by developing innovative diagnostic assays and instruments that are trusted by healthcare providers around the world.

Our broad offering of diagnostic tests and Licensed Technology solutions, made available thanks to ongoing investments in research, positions us as the player with the widest range of specialty solutions in the sector and identifies us as the "Diagnostics Specialist."

Why Join Diasorin?

• Impactful Work: When you join Diasorin, you become part of a team that's dedicated to improving lives. Your contributions will directly impact patient care, making a meaningful difference in the world.

• Global Reach & Innovation: Our work transcends borders. Joining Diasorin means collaborating with colleagues from all over the world, expanding your horizons, and contributing to global healthcare solutions at the forefront of the diagnostic industry.

Diverse and Inclusive Culture: We believe in the strength of diversity, and our inclusive culture reflects this commitment. We value your unique perspective and offer a supportive, collaborative environment where everyone can thrive.

Join Our Team: If you're passionate about innovation, diversity, and making a positive impact on healthcare, Diasorin is the place for you. We're looking for passionate and talented individuals who are ready to embrace new challenges and drive healthcare solutions forward.

Are you ready to be part of a dynamic team that's shaping the future of diagnostics? Join Diasorin and become a catalyst for change in the world of healthcare. Apply today and be a part of our exciting journey toward a healthier, more connected world. Together, we can make an impact!

Job Scope

The Molecular R&D Validation Associate is responsible for conducting laboratory experimentations and investigations in compliance with Quality and Health&Safety procedures with the purpose of drafting a final report. He/she will follow all applicable regulations including, but not limited to, FDA, ISO, IVDD, and CMD/CAS requirements.

Key Duties and Responsibilities

• Assisting in drafting protocols and executing laboratory research activities, in accordance with the company’s quality policies and procedures;

• If necessary, suggesting new validation procedures while always respecting validation protocols objectives;
• Once the protocol is approved, he/she will validate the test by conducting laboratory activities;
• Analyzing the data based on performed tests and interpreting the results, interacting with internal and external scientists;

• Supporting deviations management;
• Defining a drafted report to be reviewed by scientists/managers;
• Performing other laboratory activities when necessary;
• Ensuring compliance with the Code of Ethics, the Quality Management System, the Company Policies and the Corporate Procedures.

Education, Experience, and Qualifications  

Master’s degree in a scientific discipline

Specialization: Biology, biotechnology

Experience

1 year experience in a R&D molecular diagnostics laboratory.

Technical Competencies:

• Data collection and analysis;
• Basic knowledge of statistics (standard deviation and CV percentage);
• Ability to work in compliance with the standard GMP procedures;
• Basic knowledge on nucleic acid extraction;
• PCR, RT-PCR and Real-Time PCR preferred;
• Ability to exercise judgment within defined procedures to determine appropriate action;
• Technical writing skills required;
• Basic understanding of systems data management.

Skills

• Accuracy;
• Analysis and problem solving capability;
• Team work;
• Time management;
• Good communication skills;
• Ability to work following rules and procedures

Languages:

 Basic knowledge of English language is required to read, draft and edit protocols, reports and working instructions.

Travel availability:

On demand

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.

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.