Combination Products and Medical Devices QA Lead

The Associate Director is responsible for leading Quality for Combination Products and Medical Devices (CP/MD QA) global department that supports design, development, manufacture and regulatory approval of CSL combination products, which include medical device constituent part(s) as well as the audit program to evaluate quality.

This role is accountable for the development, execution, and performance of the Global CP/MD Quality System for combination products in compliance with applicable regulations. The Quality System under the leadership of this role must define / govern quality related business processes throughout the entire combination product lifecycle, with the emphasis on the new product development activities.

The Associate Director is expected to take part in defining the overall company strategy for the combination products, as well as the strategy for the CSL Global Quality.

Reports To: Head, R&D Quality

Direct Reports: Regional Quality Engineer Combination Products and Medical Devices

RESPONSIBILITIES AND ACCOUNTABILITIES:

1. Develop, implement and manage Global CP/MD Quality System compliant with the relevant regulations, such as 21 CFR Part 4, applicable chapters of 21 CFR Part 820, MDD/MDR, as well as applicable standards (e.g. ISO 13485). The Quality System must define quality related activities throughout the entire combination product lifecycle from the product concept through commercialization, with the emphasis on the new product development activities for all CSL Behring combination products. Processes governed by CP/MD Quality System must include but are not limited to: Design Controls for the combination products (including risk management); CP/MD vendor management; post-market surveillance and quality reviews.

2. Direct appropriate budget and resource management within CP/MD QA by strategic assessment of workload, required planning for staffing, coordination of consultant activities as needed and on-going review of forecasted expenditures. Ensure appropriate allocation and utilization of Global CP/MD QA resources. Develop, train and mentor CP/MD Quality staff.

• Developing and implementing Design Control process, as a part of CP/MD Quality System, in compliance with the requirements of 21 CFR Part 820.30, ISO 13485, MDD/MDR and other relevant regulations, as well as applicable standards (e.g. ISO 14971, IEC 62366-1). Design Control processes must incorporate appropriate quality engineering techniques such as risk analysis, statistical data analysis, sampling plan development, etc.
  
• Assigning resources to on-going R&D/Technical Development CP/MD projects to ensure that design development work is compliant with the applicable regulatory requirements and follows the Design Controls process. CP/MD oversight is provided for the internal design development activities, as well as custom / novel medical device development conducted by qualified vendors.
  

• Developing and implementing of CP/MD QA internal auditing program
  
• Ensuring adequate level of training on the CP/MD QA processes across impacted functions by developing and delivering training courses (e.g. Design Controls, Risk Management, etc.)
  

• Play an active role in defining the overall company strategy for the combination products and Connected Health including: integration of the CP/MD requirements into existing CSL Behring processes and functional structure, development of comprehensive combination products portfolio including platform solutions; proactive assessment of changing regulatory requirements and timely implementation.
  
• Contribute ideas to the larger strategic vision of Global Quality (including R&D QA) and interact with the respective Leadership Team to ensure continuous alignment on vision.
  

• Minimum of 10 years of experience as a quality, engineering or manufacturing professional in medical devices or combination products industry. May consider candidates with pharmaceutical, biotech or other related background.
  
• Progressively more responsible positions in a complex organization and experience working in a regulated environment.
  
• Minimum of 2 years of experience in people management, including leading, developing and managing on-site and remote employees.
  
• Experience in managing multi-site locations preferred.
  
• Experience in budgeting and financial management preferred.
  

• Strong leadership role with experience in medical device and/or combination product field and working knowledge of the international and national regulations, at minimum, 21 CFR 820, 21 CFR Part 4, ISO 13485, ISO 14971, EU MDD / MDR, relevant FDA guidances, industry standards and their application in a compliant QMS.
  
• Extensive practical experience in medical devices R&D Quality: new product development life cycle, design controls, requirement specifications, risk management (including FMEA), validation / verification (V&V), usability / human factor studies, DHFs, DMRs.
  
• Experience in the development, implementation and oversight of Quality Systems.
  
• Excellent oral and written communication skills, ability to communicate effectively to all levels of the business.
  
• Strong collaboration, influencing and negotiation skills to allow working effectively across a matrix organization.
  
• Excellent critical reasoning, decision-making and problem solving skills to analyze complex circumstances, determine risks, and drive appropriate decisions and actions.
  
• Demonstrated strategic thinking, planning capabilities and organization skills.
  
• Experience of working in global cross-functional teams.
  
• Proficient in English and standard MS Office applications.
  

• This role requires periodic domestic and international travel.