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Associate Director, Production, Infrastructure, and Operations, Template Control

Cette offre d'emploi n'est plus active.

Localisation: Salt Lake City, UT, États-Unis
Type de Contrat: Unfixed Term
Fonction: Manufacturing

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Description

Job Summary
The Associate Director of Production, Infrastructure, and Operations in Template Control owns strategic planning for and execution of production deliverables, lab infrastructure and scale-up, production logistics and operations, facilitates process improvement initiatives, and supports new product transfer projects. These efforts support bioMérieux's in vitro molecular diagnostics research and development, manufacturing, validations, and quality control efforts. Principle responsibilities include developing and executing strategic plans for Production and Operations Teams to meet current and future product demands, maintaining lab infrastructure and onboarding equipment and instruments necessary to fulfill production and development project deliverables, administering the department process improvement program, and facilitating and strengthening interdepartmental support relationships to ensure the continued success of the team. Exceptional organizational and problem-solving skills, attention to detail, and commitment to bioMérieux’s corporate culture are essential for success as a senior member of our team.

Essential Job Duties and Responsibilities
1. Perform all work in compliance with company policy and within the guidelines of bioMérieux's Quality System.
2. Oversee general lab work and maintenance in accordance with cGMP/ISO/FDA standards.
3. Oversee material dispensation and inventory control in accordance with cGMP/ISO/FDA standards.
4. Maintain currency in company objectives, plans, priorities, and program agility in department operations.
5. Direct the Template Control production and operations teams via resource assessments and strategic planning for personnel, infrastructure, and materials based on production and development project priorities
6. Maintain clear department objectives grounded on corporate and program goals and execute plans and initiatives to meet those objectives.
7. Develop and maintain key performance indicator tracking and establish and support efforts to improve teams’ execution.
8. Train and develop Production and Operations teams’ management personnel and administer the teams’ training programs alongside managers.
9. Exemplify and inculcate BioMérieux’s positive corporate culture with production and operation teams.
10. Onboard and manage department lab and instrument infrastructure leveraging appropriate company support teams.
11. Guarantee uninterrupted supply of Template Control products via conservative inventory control, manufacturing scheduling, quality troubleshooting, scale-up projects, process improvement projects, and timely on-boarding of new processes and products.
12. Use appropriate tools to resolve process or product-related issues such as temporary deviations, rework procedures, non-conformance reports, etc.
13. Oversee quality investigations including problem identification, data analysis and review, corrections and corrective action, preventative actions, and timely completion of documentation leveraging nonconformance reporting.
14. Coordinate with team Managers, Supervisors, Project Managers, Scientists, Research Associates, and other personnel in new process/product implementations into Template Control.
15. Facilitate scheduling and resourcing of process improvement project studies, experiments, instrument, analytical method, and process validation efforts, and other tasks in support of department projects.
16. Originate, review, and support document revision efforts.
17. Other responsibilities and tasks as assigned.

Qualifications
Training and Education
• Bachelor’s degree (biology or chemistry preferred) and a minimum of 5 years full-time work experience in a regulated field
Or
• Master’s degree/PhD in related field, and a minimum of 3 years full-time work experience in a regulated field.

Experience
• 5 years of full-time experience in a management role preferred
• 2 years of work experience in the medical device industry required
• Familiarity with ISO 9001, 13485, MDSAP, 21 CFR 820 strongly preferred
• Familiarity with cGLP and cGMP strongly preferred
• Familiarity with PCR and its variants strongly preferred
• Professional certifications preferred, including Six Sigma, 6s, Kaizen, Lean, etc.

Knowledge, Skills and Abilities
• Ability to utilize well-developed interpersonal communication skills and practiced emotional intelligence to successfully relate with and motivate personnel at all organizational levels.
• Ability to develop, coordinate, and implement multi-level individual and team-based skills.
• Ability to organize, lead, and objectively evaluate the work of others.
• Leverage practical managerial skills, including computer literacy in database, spreadsheet, project management, word processing software, and enterprise resource planning infrastructure.
• Ability to write detailed and succinct reports, reviews, and manufacturing procedures.
• Ability to define problems, collect data, establish facts, and draw valid conclusions.
• Ability to assimilate and advance bioMérieux’s corporate culture of purpose, opportunity, success, appreciation, well-being, and leadership.

Physical Requirements
Must be able to work at a desk for extended periods.
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