Quality & Compliance Manager

Peregrine Surgical LTD•Doylestown, PA

11h•Onsite

About The Position

Dutch Ophthalmic USA is part of DORC (Dutch Ophthalmic Research Center), which manufactures equipment, instruments, and liquids used in eye surgery. Every day, our employees ensure that eye surgeons worldwide benefit from innovative ophthalmic devices, instruments, and liquids. DORC utilizes cutting-edge technology, collaborates closely with innovative surgeons, and strives to make a difference. Ophthalmologists globally use our advanced Ophthalmic surgery unit EVA to care for their patients and help them see again. DORC is a ZEISS company, a leading international technology enterprise that develops, manufactures, and sells highly innovative products and solutions in various fields, including medical technology. As a foundation-owned company, ZEISS is rooted in and committed to responsibility in all its activities. As Quality & Compliance Manager, you will lead and oversee the Quality Management System (QMS) across three US entities, ensuring harmonization while maintaining compliance with FDA, ISO 13485, and applicable federal and state regulations governing medical device and pharmaceutical distribution activities. This role defines and executes the regional quality and compliance strategy, serves as the US Management Representative and primary liaison with regulatory authorities, and ensures that products released to the US market meet all regulatory and quality requirements. The position drives continuous improvement, audit readiness, effective corrective and preventive actions, and provides leadership to the quality team to sustain best-in-class compliance performance.

Requirements

Minimum 5 years in a senior role in Quality Assurance in medical device or pharma industry.
Solid understanding of quality system requirements set by the major regulatory frameworks for medical devices and combination products.
Relevant experience in managing and overseeing quality aspects in distribution, preferably in disposable devices as well as pharmaceutical products.
Ability to effectively translate quality requirements into practical directions for the organization.
Experience in management of FDA and/or Notified Body inspections
High level of integrity and ethical standards.
Ability to multi-task and methodically manage projects based on business priorities and resource availability.
Ability to self-motivate and work independently in a geographically separated multi-national and multi-functional team environment.
Collaborates effectively across a diverse network.
Open-minded for improvement opportunities and change towards striving for best-in-class compliance performance.
Ability to think creatively, proactively identifying alternative solutions to problems.
Experience in people management.
Effective communication/interpersonal skills.
Fluent in English (written and spoken).
Advanced level in Microsoft Office suite applications.

Responsibilities

Set the organizational and compliance strategy for the QA organization in the US in collaboration with the Zeiss Global Quality team.
Ensures that the commercial and distribution activities are conducted per a QMS that ensure compliance to federal and state regulations for devices and pharmaceutical products.
Manage and harmonize the QMS across the three US sites while respecting each site’s unique processes.
Develop, implement and maintain quality policies and documentation.
Acts as the local representative of DORC for regulators in North America on Quality and Compliance topics.
Accountable for verification that DORC products that are released for distribution on the US market meet specifications and regulatory requirements such as ISO13485 or FDA regulations.
Accountable for timely and effective executing and reporting of field corrective actions in North America.
Executes management oversight on all locations in North America where DORC carries responsibility for FDA regulated activities.
Reports to HQ on the effectiveness and level of compliance in DORC sites in North America through management review and other management oversight meetings.
Drives continuous improvement of QMS governed processes aimed at increasing efficiency, effectiveness, harmonization and compliance.
Prepare for and host external audits at DORC sites in North America and drive resolution of associate non-conformities.
Address non-conformities and implement corrective actions.
Educate, train and advise the organization on quality and compliance matters.
Initiate improvement projects & initiatives.
Timely escalation and resolution of quality or compliance concerns.
Act as Management Representative for each US site (Exeter, MVI, Peregrine), ensuring compliance with applicable regulatory and QMS requirements.
Leads and directs the quality teams at each site, serving as the local Head of Quality and ensuring alignment, performance, and effective implementation of quality strategies.
Ensures communication and aligns priorities between site management and the respective QA team.
Oversee risk management strategies (tbc).
This position may require serving as the facility’s Designated Representative for state licensure related to pharmaceutical and medical devices activities and undergoing background checks and fingerprinting as part of the licensure process.