The Manager Quality Engineering is responsible for the management direction and coordination of all quality and regulatory compliance activities across the designated Columbus Manufacturing BU in compliance with world-wide regulations business strategies and customer needs. This includes providing the quality leadership encompassing Quality Systems Quality Engineering and Sterilization control to ensure that the required production quality and regulatory standards are achieved through molding assembly packaging sterilization and product release. Reports to the site Associate Director Quality Management with dotted line reporting to the designated BU Manager.
ESSENTIAL FUNCTIONS (RESPONSIBILITIES)
Essential functions include but are not limited to the following:
Manages and leads the Quality Systems and Quality Engineering activities for the designated BU.
Manages and support validation activities related to processes products materials and projects supporting the designated BU and other BUs when requested.
Develops and implements strategic direction for the designated BU consistent with Hypodermic Platform MDS and BDX Quality strategy.
Provides effective Quality Management leadership to designated BU BLT and contributes to the Columbus Quality leadership Team in order to meet quality business and organizational objectives of the BD Medical: Medication Delivery Solutions.
Provides effective leadership in teamwork development effective communication and quick responses to customers. Drives improvements towards customer centricity.
Implements effective CAPA process focused on reduction of causes of customer complaints non-conformances excursions rejections and waste.
Assesses and builds organizational capability for Quality management particularly in the selection and mentoring of dedicated high caliber QEs and QC Reps (Quality Engineering and Quality Representatives) professionals.
Evaluates facilitates designs implements and continually improves quality systems and business processes including product controls to achieve quality goals and to maintain a high level of regulatory compliance.
Management representative for the designated BU with regards to all Quality System regulation issues.
Enhances BD Columbus designated BU management s understanding and application of broad scope Quality Management principles through education training and workshops.
Provides leadership and guidance in integrating Quality Management and continuous improvement into the Columbus business strategic planning process.
Champions the needs of both internal & external customers by factoring these needs into planning & decisions at all levels.
Builds a strong interactive working and strategic relationship with appropriate designated Platform Quality R&D and Regulatory management groups.
Builds & sustains a Columbus business culture that accepts Excellence as an expectation compliance as an outcome and goal.
Provides coaching and facilitation support to all levels at the designated BU Columbus plant.
Interfaces with Regulatory Agencies (FDA ISO notified body other foreign regulatory bodies).
Leads and supports customer audits internal audits.
Recommends and implements necessary actions and programs to continually upgrade the Quality Management/Quality System/Quality Engineering capability of the designated BU.
Engage and deploy zero customer complaints program.
Support the designated BU to meet: CPM Financial goals Waste target CI projects Deliveries Zero past due CAPA BBQ 5S.
Other duties as assigned.
REQUIREMENTS
Bachelor of Science degree in Engineering or Science related field.
Minimum 5 years experience in quality with a minimum of 3 years in the medical device industry
Experience with Validations CAPA Statistical Analysis.
Experience with high volume manufacturing processes.
Experience in Lean/Six Sigma.
Experience managing and leading people required.
Experience communicating with all levels of the organization.
Capable to manage under pressure and set priorities accordingly.
Full support to a 24/7 operation.
Security Clearance Required: No
Visa Candidate Considered: No
Job Description:Industry: Manufacturing & ProductionJob Category: Manufacturing - QualityThe Manager Quality Engineering is responsible for the management direction and coordination of all quality and regulatory compliance activities across the designated Columbus Manufacturing BU in compliance with...
Job Description:
Industry: Manufacturing & Production
Job Category: Manufacturing - Quality
The Manager Quality Engineering is responsible for the management direction and coordination of all quality and regulatory compliance activities across the designated Columbus Manufacturing BU in compliance with world-wide regulations business strategies and customer needs. This includes providing the quality leadership encompassing Quality Systems Quality Engineering and Sterilization control to ensure that the required production quality and regulatory standards are achieved through molding assembly packaging sterilization and product release. Reports to the site Associate Director Quality Management with dotted line reporting to the designated BU Manager.
ESSENTIAL FUNCTIONS (RESPONSIBILITIES)
Essential functions include but are not limited to the following:
Manages and leads the Quality Systems and Quality Engineering activities for the designated BU.
Manages and support validation activities related to processes products materials and projects supporting the designated BU and other BUs when requested.
Develops and implements strategic direction for the designated BU consistent with Hypodermic Platform MDS and BDX Quality strategy.
Provides effective Quality Management leadership to designated BU BLT and contributes to the Columbus Quality leadership Team in order to meet quality business and organizational objectives of the BD Medical: Medication Delivery Solutions.
Provides effective leadership in teamwork development effective communication and quick responses to customers. Drives improvements towards customer centricity.
Implements effective CAPA process focused on reduction of causes of customer complaints non-conformances excursions rejections and waste.
Assesses and builds organizational capability for Quality management particularly in the selection and mentoring of dedicated high caliber QEs and QC Reps (Quality Engineering and Quality Representatives) professionals.
Evaluates facilitates designs implements and continually improves quality systems and business processes including product controls to achieve quality goals and to maintain a high level of regulatory compliance.
Management representative for the designated BU with regards to all Quality System regulation issues.
Enhances BD Columbus designated BU management s understanding and application of broad scope Quality Management principles through education training and workshops.
Provides leadership and guidance in integrating Quality Management and continuous improvement into the Columbus business strategic planning process.
Champions the needs of both internal & external customers by factoring these needs into planning & decisions at all levels.
Builds a strong interactive working and strategic relationship with appropriate designated Platform Quality R&D and Regulatory management groups.
Builds & sustains a Columbus business culture that accepts Excellence as an expectation compliance as an outcome and goal.
Provides coaching and facilitation support to all levels at the designated BU Columbus plant.
Interfaces with Regulatory Agencies (FDA ISO notified body other foreign regulatory bodies).
Leads and supports customer audits internal audits.
Recommends and implements necessary actions and programs to continually upgrade the Quality Management/Quality System/Quality Engineering capability of the designated BU.
Engage and deploy zero customer complaints program.
Support the designated BU to meet: CPM Financial goals Waste target CI projects Deliveries Zero past due CAPA BBQ 5S.
Other duties as assigned.
REQUIREMENTS
Bachelor of Science degree in Engineering or Science related field.
Minimum 5 years experience in quality with a minimum of 3 years in the medical device industry
Experience with Validations CAPA Statistical Analysis.
Experience with high volume manufacturing processes.
Experience in Lean/Six Sigma.
Experience managing and leading people required.
Experience communicating with all levels of the organization.
Capable to manage under pressure and set priorities accordingly.
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