Senior Manager, RDQA

The Senior Manager, R&D Device Quality will support the development of medical devices and/or device components of combination products by providing directions on applicable design control, human factors/usability engineering, and risk management processes. This position will engage with all areas involved in the product development process and provide direction and consultation assuring the design control system is effectively established, executed, and maintained. This position will participate in product risk assessment efforts, including hazard analysis and design failure mode effect analysis, and development of the risk management plans.

Responsibilities:

• Provides quality system methodology guidance, support and review for medical device products throughout the design and development and change control processes.
• Actively participates in cross-functional design teams assessing design documentation for quality characteristics, including product requirements, safety risk management, design verification, design validation, manufacturability, serviceability, biocompatibility, sterilization, packaging and reliability.
• Works with product development engineering and manufacturing engineering to translate design requirements into manufacturing requirements to achieve design for manufacturability.
• Serves as a technical resource for problem investigations to guide root cause analysis / corrective action development.
• Facilitates and leads design and reliability activities related to Design, Manufacturability, and Reliability (DRM) practices. This includes planning, leading, facilitating, and supporting activities such as robust engineering, reliability predictions, capability analysis, development of CTQ's, VOC, requirements flow down, etc.
• Ensure that product development projects and changes to existing products are conducted in compliance with the FDA Quality System Regulation, ISO 13485 Regulations, and other applicable standards.
• Provide quality oversight for clinical batch manufacturing, including equipment qualification, adherence to approved processes, data traceability, and clinical batch release.
• Develop and implement site QA strategies, improve design control and risk management processes, support a consistent and compliant MDCP quality management system, oversee Operations QA activities, and contribute to CAPA investigations and resolution.
• Support regulatory audits and inspections as subject matter expert, while driving quality harmonization, data-informed improvements, and initiatives that enhance process effectiveness and product performance.
• Maintains expertise in both current and emerging requirements and quality trends as they relate to Pharmaceuticals and Medical Devices worldwide.
• Supports changes to quality standards to ensure conformance and continuous improvement.

• 10+ years’ experience working in the Medical Device industry, 2+ years in project management
• Minimum of a BS in Engineering or Scientific discipline; MS preferred
• Strong knowledge of Medical Device development activities
• Proven expertise with interpreting, applying, and leading others in compliance with 21 CFR Part 820 Quality System Regulation, ISO 13485 Quality Standard, ICH Q9 Guidance for Industry – Quality Risk Management, 21 CFR 4 Regulation of Combination Products, SOR 98-282 Canadian Medical Device Regulation, ISO 14971 Risk Management Standard, MDD, IEC/EN 62366 Application of Usability Engineering to Medical Devices, and ANSI HE75 Human Factors Engineering in Design of Medical Devices
• Skilled in requirements analysis, including testable and measurable specifications
• Familiar with reliability analysis and test methods and test method validation
• Good verbal (including presentation) and written communication skills, especially technical report writing
• Ability to effectively influence others and work within the Allergan organization as well as partnering with external partners
• Experience interacting with regulatory agencies and notified bodies
• Good knowledge and experience with corrective action and preventive action system, statistical process control, quality risk management, FMEA, DOE and other key tools for managing quality performance

Applicable only to applicants applying to a position in any location with pay disclosure requirements under state or local law: ​

• The compensation range described below is the range of possible base pay compensation that the Company believes in good faith it will pay for this role at the time of thisposting based on the job grade for this position. Individual compensation paid within this range will depend on many factors including geographic location,and we may ultimately pay more or less than the posted range. This range may be modified in the future. ​

• We offer a comprehensive package of benefits including paid time off (vacation, holidays, sick), medical/dental/vision insurance and 401(k) to eligible employees.​

• This job is eligible to participate in our long-term incentive programs. ​

Note: No amount of pay is considered to be wages or compensation until such amount is earned, vested, and determinable. The amount and availability of any bonus, commission,incentive, benefits, or any other form of compensation and benefits that are allocable to a particular employee remains in the Company's sole and absolute discretion unless anduntil paid and may be modified at the Company’s sole and absolute discretion, consistent with applicable law.​

AbbVie is an equal opportunity employer and is committed to operating with integrity, driving innovation, transforming lives and serving our community. Equal Opportunity Employer/Veterans/Disabled.

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