Senior Manager Manufacturing QC 6784
Senior Manager Manufacturing QC 6784
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$ 132750 - 165250
1 Vacancy
Job Description
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
Guarantees efficient and effective production and packaging processes of components and finished products and control of raw materials components and finished products for the LIAISON product lines of the Stillwater site in accordance with the production plans and in compliance with the requirements of Quality managing the investigation activities in case of NonConformities and/or Complaints attributable to the functioning and packaging of the materials/products.
Manages the team of coordinators of the Quality Control laboratories.
Implements programs aimed at improving the control processes of the products of competence and collaborates in the management of the plant quality system periodically reporting on the results and progress of the activities and promoting actions to improve the system in the area of competence.
Collaborates with the Research and Development staff in the transfer of new projects within the company and with external bodies with a view to optimizing/introducing technologies and analytical methods. Supports the Analytical Methods Development team in the implementation of development projects.
Key Duties and Responsibilities
Ensure the production and primary and secondary packaging of components/kits according to the plans agreed with Logistics;
Ensure immunometric controls of raw materials semifinished products and finished products ensuring the correct maintenance of the standards and necessary materials;
Ensure the synchronization of activities between Production Quality Control and Packaging within the times agreed with Planning and in compliance with preestablished methods and procedures;
Manage the Material Acceptance Quality Control activities within the QC & Manufacturing group in the Operations area.
Ensure the correct coordination of the activities of the Microbiological QC the ChemicalBiochemical QC and the Dimensional QC ensuring the maintenance of the times and quality standards;
Interact with the Warehouse Planning and Procurement areas in order to guarantee the correct of the activities aimed at guaranteeing the presence of approved and functional raw materials necessary for the production of the diagnostic kit
Coordinate the analytical methods development team in the validation and application of the principles required by current regulations.
Is responsible for the optimization of resources and ensures their training updating and development with particular attention to safety ecology environmental hygiene and compliance with current regulations.
Interact with QA in the technical evaluation of supplier change notifications supporting the Change/OOS/NC/CAPA evaluation activities generated internally.
Evaluate and approve for the part of his/her competence the project documentation in which he/she is involved
Define target objectives and verify the progress towards their achievement.
Assign objectives to his/her collaborators
Ensure in collaboration with the PostMarket Surveillance body the necessary studies resulting from the assessments of the Competent Authorities;
Develop and implement projects aimed at improving production and analytical processes as well as the performance of distributed products.
Education Experience and Qualifications
- Degree in technicalscientific subjects or equivalent
- At least 10 years of experience in related role in the pharmaceutical/biomedical field preferably in the Medical Device sector
- Knows in depth the assay schemes used in the company and their diagnostic meaning. Knows the flows applied to the production and packaging departments.
- Chemistry Biochemistry Biology indepth knowledge of the Quality Management System and FDA regulations
- Ability to manage and coordinate work teams.
- Project management skills.
- Excellent analytical and planning skills.
- Leadership strong orientation towards results and good stress management.
What we offer
Salary Range
The salary range for this position is $132750 $165250 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.
Required Experience:
Senior Manager
Employment Type
Full-Time
