Quality Operations Manager Johnson & Johnson 29-04-2024

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Quality Operations Manager

• Titel Quality Operations Manager
• Functie Quality
• Sub functie Quality Assurance
• Categorie Manager, Quality Assurance (PL7)
• Locatie Groningen, Netherlands
• Gepost apr 29 2024
• Referentie 24W

Beschrijving

At Johnson & Johnson, we believe health is everything. Our strength in healthcare innovation empowers us to build a world where complex diseases are prevented, treated, and cured, where treatments are smarter and less invasive, and solutions are personal. Through our expertise in Innovative Medicine and MedTech, we are uniquely positioned to innovate across the full spectrum of healthcare solutions today to deliver the breakthroughs of tomorrow, and profoundly impact health for humanity. Learn more at https://www.jnj.com/.

Manages Quality Systems application in manufacturing, materials, facilities.,, distribution, engineering and maintenance to ensure smooth, continuous, cost effective and controlled manufacture of products in support of the business' forecasts. At this level, the position has a greater degree of impact on the business results and typically, responsibility for managing a group of professionals.

• Develops, implements and maintains quality control requirements and processes.
• Communicates and enforces business objectives, policies and procedures to the department.
• Recommends revisions to standard operating procedures and observes employees to ensures compliance with business.
• Manages the proper installation and routine maintenance of processing equipment.
• Establishes systems to ensure quality control compliance. Encourages employee's leadership, motivates through regulatory compliance, rewards, job enrichment, environmental, health and safety compliance and challenging assignments.
• Supports and enforces employee's training programs, team development and integration.
• Acts as change agent in the Continuous Improvement process by fostering team formation and providing team members the necessary tools to be successful. Identifies, develops, and participates in continuous improvement projects and programs to recommend work simplification, eliminate non-value-added activities, and cost reduction.
• Follows, observes and promotes all regulatory requirements compliance applicable to the plant (QSR, ISO, FDA) rules, procedures, and internal policies, and directs training related activities to ensure compliance with procedures established by the Company, and ensures these are also followed and observed by personnel supervised.
• Addressing non-conformities within production and taking care of internal escalations.
• Advising, reviewing and (approving) changes in production processes, in line with the applicable procedures
• Analyzing data on rejects within the production process for continuous improvement and reducing or eliminating sources of variation within the production process

Kwalificaties

• Bachelor's Degree or equivalent.
• 6-8 years of experience in Quality Engineering or Quality Assurance functions within the Pharmaceutical or Medical Device Industry is required.
• 2-4 years in supervisory experience.
• Experience dealing with applicable Health Authority inspections.
• Good written and oral English communication skills.
• Ability to select, manage and direct a team as applicable.
• Ability to respond to common inquiries, regulatory agencies, or members of the business community.
• Statistical skills and manufacturing process understanding.
• Ability to lead a team through a root cause analysis problem.
• Ability to effectively present information to top management. public groups. and/or boards of directors.
• Ability to stand firm while being open to new approaches. Engages in constructive conflict.
• High tolerance for ambiguity in a complex environment. Ability to solve practical problems and deal with a variety of concrete variables in situations where only limited standardization exists.
• Ability to build partnerships both internally and externally. Ability to effectively interface with governmental and independent auditors.
• Ability to use PC's and associated Microsoft software.

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