Quality Control Associate I, Reagents

Obsessed by Science. Entrepreneurial by Nature. United by Purpose.

Diasorin is a global leader in immunodiagnostic and molecular diagnostic solutions, advancing science to improve patient outcomes worldwide. For more than 50 years, we have combined scientific rigor with an entrepreneurial mindset, operating with a strong commitment to innovation, accountability, and results to deliver trusted diagnostic solutions.

As the Diagnostics Specialist, Diasorin continuously invests in research, technology, and people. Guided by our values of operational excellence, customer focus, and teamwork, we empower teams to think boldly, act decisively, and transform ideas into meaningful impact across one of the industry’s broadest specialty diagnostic portfolios.

When you join Diasorin, you are not just filling a role. You are helping build what comes next.

Why Join Diasorin

- Build What Matters
Take ownership, challenge the status quo, and contribute directly to solutions that improve patient care worldwide.

- Innovate with Agility at a Global Scale
Work in an entrepreneurial environment that enables speed, collaboration, and global impact.

- Grow in a People-Centered Culture
Thrive in a culture that values accountability, inclusion, and continuous development.

Job Scope

The Quality Control Associate I, Reagents will be responsible for executing core Quality Control (QC) processes associated with reagent consumable and bioassay production, reagent stability program, and controlled storage monitoring, assisting with incoming quality control, departmental calibration and maintenance and the retention program and maintaining QC laboratory supplies, preparing internal use laboratory reagents, as well as maintaining the integrity and cleanliness of QC work and storage areas. This position will be participating in QC processes associated with test method development, product development, and equipment/ method validations and have frequent intra-department interaction as well as frequent inter-department interfaces with Quality Assurance, Reagent Manufacturing, Design Transfer and Process Engineering, Production Planning, Purchasing, and Document Control.

Key Duties and Responsibilities

- Deliver timely and accurate Quality Control testing for bioassay and core consumable products.

- Deliver timely and accurate completion of quality control and manufacturing process documentation including related business system transactions.

- Generate Certificates of Quality

- Document and complete non-conformances

- Respond appropriately to environmental monitoring notifications of specialized storage areas; includes 24/7 call list rotation

- Execute stability study sample scheduling and processing.

- Participate in program to sustain orderliness and cleanliness within related quality control and manufacturing area through routing sorting, labeling, systematic cleaning, and standardizing.

- Assist in timely processing of purchased materials for release including related business system transactions.

- Assist in on-time maintenance and calibration of Reagent QC measuring and monitoring devices

- Schedule timely outsource testing and services with associated documentation of results.

- Assist in monitoring of departmental supplies and stocking of focused Reagent QC supplies; generate Purchase orders as needed.

- Assist in filing retentions and retention maintenance program.

- Prepare laboratory reagents for internal use

- Deliver timely and accurate completion of inventory cycle counts for select sub-inventories.

- Participate in applicable departmental and interdepartmental training

- Maintain current training to standard operating procedures, quality control instructions (QCIs), and applicable changes affecting quality control.

- May assist in training of QC Technician and QC Associates to task-specific operations.

- Assist in investigation and resolution of findings impacting Reagent Quality Control initiated through audits, non-conformances, corrective/preventive actions, or customer complaint escalation.

- Assist in the execution of validations of test methods, equipment, and processes.

- Assist in the review or revision of reagent QCIs, manufacturing instructions, and SOPs as required.

- Support design transfer and the integration of new products and processes

- Support process development and process improvement projects.

- Assist in compilation of technical deliverables as required.

- May participate in infrastructure improvements affecting quality control.

- Maintain effective and professional multi-level organizational interfaces

- Ensure personal compliance with Quality System; facilitate sectional compliance with the Quality System.

- Adhere to safety, disposal and gowning requirements applicable to department; facilitate departmental safety compliance.

- Participate in additional quality activities as required

- Other duties as assigned

Education, Experience, and Qualifications

- Bachelor's Degree B.S. in Chemistry, Biochemistry, Biology, or related science discipline required

- 1+ Years At least 1 year of relevant experience in a Life Sciences, Chemistry, or Medical Technology related industry preferably in an FDA regulated and/or ISO certified operation required

Standard Physical Demands

- Standing - Occasionally

- Stooping - Occasionally

- Bending - Occasionally

- Climbing - Occasionally

- Sitting - Occasionally

- Kneeling - Occasionally

- Lifting of at least 40lbs - Occasionally

What We Offer

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. Benefits may vary by role, country, region, union status, and other employment status factors. 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 committed to building a workplace where people feel empowered to contribute ideas, take ownership, and grow their careers. We believe diverse perspectives strengthen innovation and help us deliver meaningful impact for patients and customers worldwide.

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, disability, protected veteran status, or any other characteristic protected by applicable law.

This posting and recruitment process are subject to applicable local laws and regulations in the country where the position is located. Additional employment disclosures, candidate rights, and employment conditions may apply based on local jurisdiction.

Individuals hired will be required to verify identity and eligibility to work and may be subject to a background check and drug screening where permitted by law. Diasorin is committed to providing reasonable accommodations for qualified individuals with disabilities during the application process. If assistance is required, please contact [email protected] .

​Recruitment Fraud Notice

Diasorin never requests payment, financial information, or personal banking details from candidates at any stage of the recruitment process. Official communications from Diasorin recruiters will only come from a verified @diasorin.com email address. If you have questions about the legitimacy of a recruitment communication, please contact [email protected] for verification.

Unauthorized third-party recruiting agencies may not submit candidates for this position without prior written authorization from the Diasorin Human Resources Department.