Production Manager

diasorinsp•Cypress, CA

1d•$128,700 - $174,100

About The Position

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 MattersTake ownership, challenge the status quo, and contribute directly to solutions that improve patient care worldwide. Innovate with Agility at a Global ScaleWork in an entrepreneurial environment that enables speed, collaboration, and global impact. Grow in a People-Centered CultureThrive in a culture that values accountability, inclusion, and continuous development.

Requirements

Bachelor's Degree (BA/BS) Required
4+ Years direct manufacturing supervision experience in ISO9001, ISO13485 or cGMP environment, three (3) years in a biological products production facility subject to Good Manufacturing Practices (GMP) or Good Laboratory Practices (GLP) or an equivalent combination of related work experience Required
Prior experience in developing new product documentation, processes and practices including design transfer responsibility. Required
Demonstrated leadership, facilitation and project management experience is required.
Incumbent must have excellent written and oral communication skills and be able to exhibit strong leadership, interpersonal, and teamwork skills.
Ability to read, analyze, and interpret general business periodicals, professional journals, technical procedures, or governmental regulations.
Ability to write reports, business correspondence, and procedure manuals.
Ability to effectively present information and respond to questions from groups of managers, clients, customers, and the general public.
Ability to calculate figures and amounts such as discounts, interest, commissions, proportions, percentages, area, circumference, and volume.
Ability to apply concepts of basic algebra and geometry.
Ability to apply common sense understanding to carry out instructions furnished in written, oral, or diagram form.
Ability to deal with problems involving several concrete variables in standardized situations.
MS Word, Excel and PPT skills; familiarity with Google Suite

Nice To Haves

Experience with Six Sigma/Process Excellence Tools, Training, and/or Certification Preferred
Working knowledge of cell culture, sterile products, protein purification, in-vitro diagnostic production, and technical knowledge of infectious bacteria, viruses and related products is preferred.

Responsibilities

Responsible for directing the development, planning, implementation and maintenance of manufacturing methods, processes and operations for new or existing products and technologies.
Ensures the effective use of material, equipment and personnel in producing quality products.
May monitor and control labor and capital expenditures.
May assist in developing budgets.
Formulate and recommend manufacturing policies, procedures and programs.
Write procedures, specifications, protocols, production records and other required documents.
Support all applicable regulations including but not limited to FDA, ISO, and CMD/CAS requirements.
Insure timely and quality delivery of products and services to both internal and external customers and be accountable for meeting objectives including production plans and budgets.
Take an active role in value improvement projects, (i.e., Lean Initiatives, quality, production cell development, equipment validations, new product launch production plans).
Use sound root cause investigation to address quality and scrap issues and develop effective corrective actions for non-conformance issues identified by the quality system.
Participate in the technical transfer, planning, implementation and maintenance of manufacturing processes including the transition of new products and processes.
Work closely with Cell Culture and Purification development groups creating a team environment for the scale-up of production operations, processes and optimization of procedures.
Identify problems, areas for improvement, and provide input on technology transfer and support to engineering, PDP and technical support departments.
Develop standard cost models and use of materials, labor and machines which affect standard costs in order to ensure performance at standards and to provide costing data for use in the annual budget process.
Develop and revise operating metrics, manufacturing specifications and procedures, protocols, studies and other documents as needed, by the Company.
Track performance to metrics as needed to insure attainment of company goals and blueprint.
Lead and facilitate process improvement teams, managing the technical issues that affect the production floor, and identifying and implementing capital projects.
Select, train and evaluate staff, maintain compliance in all safety, QSR, environmental and contract areas, and exercise direct supervision over various departments and production employees with respect to meeting production schedules and delivery dates.
Analyze annual staff performance and conduct performance reviews.
Manage Succession Plans to ensure efficient operation of department.
Perform assigned tasks in accordance with applicable Environmental Health and Safety (EHS) regulations and Company EHS policies.
Lead the manufacturing of raw material and its transformation into finished product through direct supervision and leadership of hourly manufacturing and other professionals.
Develop and implement activities in production area(s) to meet production goals, quality, and cost objectives.
Ensure that team is properly trained in cGMPs, procedures, good documentation practices and regulatory matters.
Monitor personnel practices to ensure compliance with SOPs, practices and regulations.
Participate in design and implementation of training, cross-training and development programs.
Enforce all EHS policies in span of control.
Perform other duties as assigned.