Senior Quality Control Manager Reagents 6610

Diasorin is a global leader in diagnostic solutions pushing the boundaries of science and technology to create cuttingedge tools that improve healthcare worldwide. With a legacy spanning over 50 years weve 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 thats 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 youre passionate about innovation diversity and making a positive impact on healthcare Diasorin is the place for you. Were 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 thats 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:

• Manages associated Quality Control staff of moderate to high span of control and/or skill level.
• Leadership position that provides direct oversight to the Reagent Quality Control areas as well as leads and participates in crossdepartmental/organizational teams.
• Responsible for ensuring facilities resources and equipment are in place to deliver product to the business plan.
• Accountable for quality control support of new product integration stability program process development equipment and process validations as well as meeting production schedules.
• Promotes and maintains Company Objectives and Quality Policies.
• Manufacturing environment is a high complexity small/large run production environment. Responsible for standard and custom Luminex reagent product lines manufactured in an environment that is ISO certified and includes products that are FDA regulated.

Key Duties and Responsibilities:

• Oversee direction planning and of Reagent Quality Control operations and associated personnel.
• Drive attainment of production schedule for finished product qualification/processing of incoming materials production intermediates and stability sample testing.
• Develop and implement approved departmental procedures policies and processes.
• Deliver reagent quality control design transfer requirements for new and changed product through validation and market release phases.
• Establish manage and deliver timely reporting of departmental performance metrics and statistical process controls; drive actions as required.
• Lead/Manage or assist in planning prioritization development and implementations of new local and multidepartment improvement initiatives policies and programs.
• Deliver efficiency cost reduction and quality improvement projects within scope of department as defined to organizations goals.
• Lead or participate in sustaining projects for improvement of processes global harmonization infrastructure product specifications process/test methods analysis tools and business systems.
• Oversee and participate in Change Control Board responsibilities for Reagent Quality Control as needed.
• Lead or participate in investigations and resolution of findings impacting the Reagent Manufacturing Organization identified through audits nonconformances corrective/preventive actions or customer complaint escalations.
• Establish and maintain appropriate departmental rolespecific training plans; ensure that each team member is properly trained on systems processes and equipment.
• Identifies and manages annual departmental capital headcount and expense budgeting requirements.
• Monitor and appraise personnel performance; develop and advance personnel consistent with needs of organization.
• Drive departmental strategic planning encompassing organization equipment and facilities.
• Recommend and/or manage development of new departmental process capabilities and equipment.
• Maintain personal compliance and facilitate departmental compliance with the Luminex Quality System.
• May manage Material Review Board and deliver operational nonconformance disposition approval.
• May lead the administration of reagent certificate of quality/analysis program to include certificate issuance.
• May manage quality control specific labor routings and lead times for optimal accuracy; facilitate definition of labor routings and lead times for new product introductions.
• May administer 24/7 environmental monitoring infrastructure and program for specialized storage areas and ensure continuous readiness and effectively respond to environmental monitoring notifications.
• Other duties as assigned.

Education Experience and Qualifications:

• Bachelors Degree Field of chemistry biological sciences or related field degree. required

• 8 Years Relevant Quality Operations leadership experience required
• 10 Years Relevant experience in a manufacturing environment in an FDA regulated industry and/or ISO certified organization with a Bachelors Degree required

• Mathematics aptitude (High proficiency)
• ISO 13485 and FDA Quality Systems knowledge (High proficiency)
• Proficiency in use of process based Manufacturing Resource Planning systems such as Oracle or SAP (High proficiency)
• Proficiency in the use of Product Life Cycle Management tools (High proficiency)
• Proficiency in data analysis tools and technical writing (High proficiency)
• Knowledge in clean room operations molecular grade processing/purified water systems (High proficiency)
• Applied knowledge of process equipment and test method validations (Medium proficiency)
• Functional knowledge of nucleic acid immunoassay and serology assay chemistry (Medium proficiency)
• Statistical aptitude (Medium proficiency)
• Quality Certification such as ASQ CQM CQE or Sixth Sigma Certification preferred

Travel Requirements

• 10 Travel may be required

What We Offer

Receive a competitive wages and benefits package as you grow your career at Diasorin. Join our team and discover how your work can impact the lives of people all over the world.

Salary Range
The salaryrange for this position is $92891.00$130493.00 annually.The salary range for this role represents the numerous factors considered in the hiring decisions including but not limited to educations skills work experience certifications etc. Beyond base salary Diasorin offers a competitive rewards package focused on your overall wellbeing. 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 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 orto 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 preemployment background check and drug screen subject to applicable laws and regulations.

This position is not eligible for partnership with a thirdparty search firm vendor without expressed written consent from the Diasorin Human Resources Department.