Director, Design Assurance
Company: Disability Solutions
Location: Libertyville
Posted on: February 3, 2025
Job Description:
We Make Life More Rewarding and Dignified
Location: Libertyville
Department: Quality Summary:The Director, Design Assurance is
responsible for implementing and maintaining the effectiveness of
Validation (i.e. Product, Process, Equipment, Software, Test
Method, Utilities), Design Controls and Product Lifecycle Risk
Management processes throughout the company ensuring that there is
a systematic application of policies, procedures, and practices. As
a member of the Global Quality & Regulatory Affairs Senior
Leadership team this role represents the Global Quality &
Regulatory Affairs organization in activities related to product
changes and New Product Introductions ensuring ongoing oversight
and communication to the organization broadly. Hollister
Incorporated operates in a hybrid work environment. This position
can be located in Libertvyille, IL or Ballina,
Ireland.Responsibilities:
- Develop, maintain and execute strategies to optimize Design
Controls, Validation and Product Lifecycle Risk Management
processes and ensure compliance and connectivity to the broader
corporate requirements.
- Directly responsible for the effective organization,
administration, training, and supervision of all aspects of Design
Assurance, Validation & Risk Management ensuring oversight, cross
functional collaboration and best practices employed during product
changes and new product introductions.
- Define clear roles and responsibilities for all functions to
ensure effective execution of validation, design controls and
product lifecycle risk management processes (R&D, Regulatory
Affairs, Project Management Office, Operations, Clinical, Quality,
Global Marketing, Global Engineering).
- Ensure timely communication with key stakeholders including the
VP of Global Quality and Senior Leaders on critical validation,
design quality and risk management activities.
- Manage resources as they relate to Validation, Design Assurance
& Risk Management to support product launches, appropriately
matching skill set of individual direct reports to demands of
projects, prioritizing efforts, anticipating technical issues and
assuring successful project outcomes.
- Conduct/Coordinate regular and robust design reviews that
provide assessment of issues, risks, and resource requirements for
all phases of NPI projects.
- Ensure that product/process/package/label/Test
Method/Specification designs and associated documentation comply
with applicable Regulations for products distributed globally
(US/OUS).
- Pro-actively monitor trends linked to the product lifecycle
phases (Development, design, production, distribution,
postproduction) to ensure any potential design or quality risks are
addressed in as timely a manner as possible.
- Work closely with the R&D and Global Quality teams to
ensure robust new product launch planning and successful design
transfer process.
- Validation, Design Controls and product lifecycle risk
management SME and person directly responsible to represent the
company with outside Regulatory authorities (FDA, NMPA, Notified
Bodies, MoH, WHO) on design quality and Regulatory Agency
inspections.
- Collaborate with Regulatory Affairs and R&D to establish
appropriate product filing strategies and provide necessary product
documentation for submission.
- Collaborate with R&D, Engineering, Quality & Operations in
the development of Validation test protocols and study plans and
ensure both test plans and reports are compliant with all
applicable regulatory requirements.
- Work with R&D to ensure that Product Test Methods are
designed to provide the appropriate challenge to products and
validated appropriately.
- Establish a post launch review process that monitors new
product performance against the expected market performance and
triggers escalation/intervention as necessary.
- Ensure that GMP requirements are well understood across teams
as it relates to validation, Design controls and Product Lifecycle
Risk Management, facilitate education where required.
- Develop a risk-based approach for decision making and support
continuous improvement via development of cost-efficient processes
at sites, and collaboration between sites to optimize global
processes and share best practices.
- Advance local and global initiatives on continuous improvement
and strategic initiatives in areas of responsibility.
- Other duties as assigned.
Essential Functions of the Role:
- Job requires extensive knowledge of Medical Devices and/or IVD
design and manufacturing as well as experience in a fast-moving
R&D environment.
- Extensive knowledge of Design Controls and Product Lifecycle
Risk Management for medical devices.
- Proven track record of results managing projects in a highly
regulated environment.
- Strong Leadership capability and ability to influence change
balancing compliance with pragmatic problem solving.
- Consistent track record in delivering Continuous Improvement
programs.
- Must have strong technical ability and be articulate in message
delivery.
- Ability to work and interact with several cultures across
various time zones.
- Excellent written and verbal interpersonal skills to influence
many diverse internal and external stakeholders.
- Ability to present complex technical information to Senior
Management.
Requirements:
- Bachelor's Degree - Engineering/Science/Life Sciences - Post
graduate degree desirable in either a technical or management
discipline.
- 12-15 overall years' experience is required.
- 10 years plus experience in a QA/R&D or other technical
leadership role in a regulated environment.
- Experience managing in an environment with changing priorities
and making appropriate risk-based decisions in the face of
uncertainty.
- Experience managing a design assurance team is essential and
preferably experience working with teams remotely.
Specialized Skills/Technical Knowledge:
- Leadership experience with excellent independent judgement and
interpersonal skills, including oral and written
communication.
- Strong technical writing skills and attention to
detail
- Knowledge of 21 CFR 820, ISO 13485, ISO 14971 standards and EU
MDR regulation
- Ability to work closely with people at all levels of the
organization and with persons from different cultural, language and
regional backgrounds to accomplish assigned job
responsibilities.
- Strong leadership skills with the ability to influence change
cross-functionally and develop people
- Goal-oriented with the ability to execute on strategic
initiatives and prioritize/manage deliverables
- Good project management skills including organization and
planning.
- Able to work in a global and matrix environment
- Strong critical thinking skills applying and cultivating new
approaches to problem solving with a focus on achievement of
overall project goals
- Ability to work independently and remotely with minimum direct
supervision.
- Greenbelt certification preferred with knowledge of Lean and
Six Sigma methodology
- Knowledge of SAP ERP systems preferred.
- Strong in Microsoft Office suite, especially Excel.
#LI-HybridAbout Hollister Incorporated
Hollister Incorporated is an independent, employee-owned company
that develops, manufactures and markets healthcare products
worldwide. The company spearheads the advancement of innovative
products for ostomy care, continence care and critical care, and
also creates educational support materials for patients and
healthcare professionals. Headquartered in Libertyville, Illinois,
Hollister has manufacturing and distribution centers on three
continents and sells in nearly 80 countries. Hollister is a wholly
owned subsidiary of The Firm of John Dickinson Schneider, Inc., and
is guided both by its Mission to make life more rewarding and
dignified for people who use our products and services, as well as
its Vision to grow and prosper as an independent, employee-owned
company, and in the process, to become better human beings.Our
Total Rewards package in aggregate is above market and includes
competitive pay, paid time off programs, peer-to-peer recognition,
health and life insurance, wellness programs and incentives,
generous retirement savings, and a unique Benefit of Employee Share
Ownership Program (BESOP).
- The anticipated base salary range for this position is $155,000
- $240,000 . The actual salary varies based on applicant's
location, education, experience, skills, abilities, and other
legitimate business factors.
- If applicable: This position is also eligible to participate in
the Hollister Secure Start Bonus Plan. The Company also provides a
unique Benefit of Employee Share Ownership Program (BESOP) program
based on earnings and length of service.
- The Company's health and welfare benefits include medical,
prescription, dental, vision, spending/savings accounts,
disability, company paid (parental and caregiver) leaves, statutory
leaves/disability programs, accident, life, wellbeing, education
assistance, adoption assistance, and voluntary benefit
programs.
- The Company's 401(k) Retirement Savings Plan includes:
auto-enrollment, ROTH, vesting and eligible participants "safe
harbor" matching contributions.
- The Company's paid time off benefits include: 11 paid holidays,
paid vacation based on length of service and exempt/non-exempt
status, and sick days based on statutory requirements and/or
exempt/non-exempt status.
- The Company's additional benefits include: education assistance
and adoption assistance benefit programs.
EOE Statement
All qualified applicants will receive consideration for employment
without regard to race, color, religion, sex, sexual orientation,
gender identity, national origin, disability or protected veteran
status.Job Req ID: 33694Job Segment: Regulatory Affairs,
Compliance, Testing, Risk Management, Technical Writer, Legal,
Technology, Finance
Keywords: Disability Solutions, Milwaukee , Director, Design Assurance, Executive , Libertyville, Wisconsin
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