Manufacturing Process Quality Leader

Johnson & Johnson

Closed

Nijmegen

2 weeks ago

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Manufacturing Process Quality Leader

Johnson & Johnson seeks a Manufacturing Process Quality Leader for their Nijmegen site. The role leads process improvement, ensures compliance with QSR/GMP/ISO, and manages quality investigations. Requires a Bachelor's in Engineering/Science and 5+ years of experience in regulated medical device manufacturing.

On-siteFull-timeEntry LevelStandard Operating Procedure (SOP)QSR

Manufacturing Process Quality Leader

Apply

On-siteFull-timeEntry LevelStandard Operating Procedure (SOP)

Salary

Not specified

Work Location

Nijmegen, Gelderland, Netherlands, NL

Work Model

On-site

Experience Required

5 years

Employment Type

Full-time

Experience Level

Not Applicable

Core Qualifications

Technical (Must-have)

Standard Operating Procedure (SOP)QSRProcess ControlCAPAGMPApplied StatisticsQuality Management Systems (QMS)Failure Mode AnalysisAgile ManufacturingISOMicrosoft Office

Soft Skills

LeadershipCommunicationInterpersonal SkillsProblem SolvingTeamworkInitiativeCreativityAttention to DetailCoachingNegotiation

Key Responsibilities

•Guides team on policies and procedures for Manufacturing Process Improvement.
•Provides technical leadership for identifying causes of non-conformances and implementing corrective/preventive actions.
•Advises on cost saving measures to drive profit optimization.
•Manages operational aspects of team including workflow, performance, and compliance.
•Reviews and analyses quality trends with manufacturing team.
•Provides guidance to manufacturing supervisors for effective investigations.
•Leads cross-functional technical teams to identify root causes and implement corrective actions.
•Leads investigations of negative trends and facilitates implementation.
•Analyzes data and recommends actions for process, equipment, and system improvement.
•Writes procedures, protocols, and documentation for process enhancement.

Manufacturing Process Quality LeaderSupply Chain ManufacturingMedical DevicesQSR/ISOGMPProcess ImprovementQuality AssuranceNijmegenJohnson & Johnson

Core Qualifications

Technical (Must-have)

Standard Operating Procedure (SOP)QSRProcess ControlCAPAGMPApplied StatisticsQuality Management Systems (QMS)Failure Mode AnalysisAgile ManufacturingISOMicrosoft Office

Soft Skills

LeadershipCommunicationInterpersonal SkillsProblem SolvingTeamworkInitiativeCreativityAttention to DetailCoachingNegotiation

Key Responsibilities

•Guides team on policies and procedures for Manufacturing Process Improvement.

•Provides technical leadership for identifying causes of non-conformances and implementing corrective/preventive actions.

•Advises on cost saving measures to drive profit optimization.

•Manages operational aspects of team including workflow, performance, and compliance.

•Reviews and analyses quality trends with manufacturing team.

•Provides guidance to manufacturing supervisors for effective investigations.

•Leads cross-functional technical teams to identify root causes and implement corrective actions.

•Leads investigations of negative trends and facilitates implementation.

•Analyzes data and recommends actions for process, equipment, and system improvement.

•Writes procedures, protocols, and documentation for process enhancement.