Manufacturing Associate II, Reagents

Diasorin•Northbrook, IL

1d•Onsite

About The Position

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!

Requirements

Associate's Degree in Chemistry, Life Sciences, Biotechnology, or Medical Technology related field required
At least 3 years of relevant experience in a Life Sciences, Chemistry, Medical Technology, or Biotechnology industry required
At least 1 year of relevant experience in an FDA regulated and/or ISO certified organization preferred

Nice To Haves

Bachelors Degree in Chemistry, Life Science, Biotechnology, or Medical Technology related field preferred

Responsibilities

Deliver manufacturing requirements and attainment of production schedule for standard inventory, build-to-order, and contract manufacturing market products.
Deliver manufacturing requirements for qualification/processing of incoming materials, production intermediates, and stability samples.
Deliver timely and accurate completion of manufacturing sections of process documentation and related business system transactions.
Deliver timely and accurate completion of inventory cycle counts.
Document non-conformances and participate in Material Review Board.
Support design transfer and integration of new products and processes.
Support process development and process improvements.
Participate in the writing and execution of equipment and process validations.
Support investigations and resolution of findings impacting the Reagent Manufacturing Organization identified through audits, non-conformances, corrective/preventive actions, or customer complaints escalation.
Deliver timely maintenance and calibration of assigned Manufacturing measuring and monitoring devices.
Monitor select non-inventory supplies, maintain focused supplies, and generate purchase requisitions as needed.
Maintain cleanliness and integrity of manufacturing laboratory and storage areas.
Participate in applicable departmental and interdepartmental training; maintain current and effective training to standard operating procedures, work instructions, and applicable changes affecting the Reagent Manufacturing.
Assist in establishing annual performance goals; fulfill performance goals.
Maintain effective and professional multi-level organizational interfaces.
Maintain personal compliance and facilitate departmental compliance with the Quality System.
Adhere to safety, disposal, and gowning requirements
Update work instructions and standard operating procedures as required.
Perform change control as required to support change requirements including Engineering Change Orders, Document Change Control, and Deviations.
Assist in executing projects targeting efficiency, cost reduction, and quality improvements within scope of Bioassay manufacturing processes.
Support investigations and resolution of findings identified through audits, non-conformances, key performance indicator trends, corrective/preventive actions, or customer complaints escalation.
Participate in task-specific training of new Reagent Manufacturing Associates.
Other duties as assigned.