Assembly Lead, Consumables

at DiaSorin Inc. in Northbrook, Illinois, United States

Job Description

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 Assembly Lead, Consumables will be responsible for:
Oversight of the process, personnel, documentation, and supply requirements of building of plastic parts into a medical device cassette for use by Engineering R&D, Clinical Studies and Product Sales.
Overseeing the maintenance and/or calibration of equipment used for the manufacturing of product under the company Quality System.
Following approved cGMP manufacturing instructions and personnel are required to complete a history record of the lot built per company Quality System.
Providing feedback on the processes to assure continuous improvement by noting differences in parts, assemblies, tools, fixtures and process steps.

Key Duties and Responsibilities
Drives execution of builds to meet demands and quality system requirements
Involved in and oversees the building, testing, and visual inspection of parts, assemblies and final product according to outlined procedures
Approves DHR for Manufacturing release to QA
Maintains the integrity and cleanliness of work areas
Assures adherence to safety.
Assures proper material handling, labeling, and disposal of hazardous chemicals
Assistances in the writing and disposition of NCMRs and provide support to action investigations and associated product and process changes.
Establish an effective working partnership with other Luminex departments to promote effective communication and transfer knowledge/experience to others.
Provides leadership and training to new employees
Provide direct feedback to employees and on the manufacturing process.
Assist in the editing of procedures and or records used in the build, test, and visual inspection.
Assist in maintaining equipment integrity, performing maintenance and calibration of manufacturing... For full info follow application link.

We are an equal opportunity employer that values diversity at all levels. All individuals, regardless of personal characteristics, are encouraged to apply.

This contractor and subcontractor shall abide by the requirements of 41 CFR 60-1.4(a), 41 CFR 60-300.5(a) and 41 CFR 60-741.5(a). These regulations prohibit discrimination against qualified individuals based on their status as protected veterans or individuals with disabilities, and prohibit discrimination against all individuals based on their race, color, religion, sex, sexual orientation, gender identity or national origin. Moreover, these regulations require that covered prime contractors and subcontractors take affirmative action to employ and advance in employment individuals without regard to race, color, religion, sex, sexual orientation, gender identity, national origin, disability or veteran status.

DiaSorin Inc and DiaSorin Molecular LLC are Affirmative Action and Equal Opportunity Employers. 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.