Senior Manager, Quality Assurance

Veranex’s mission as an Innovation CRO is to improve patient outcomes by accelerating our clients’ innovations to market. As the world’s only end-to-end professional services firm focused on Med. Tech, we take clients’ Vision to Velocity through our comprehensive service portfolio, with expertise in human centered design and product development, preclinical and clinical research, regulatory affairs, and market access and reimbursement consulting.

About This Role: The experienced Senior Manager, Quality Assurance (QA) provides leadership and support to the quality assurance team. Responsible for applicable standards, regulations and guidelines in compliance for development products. This involves engaging and collaborating with cross-functional internal and external teams to evaluate processes, procedures, and activities for adherence to relevant industry standards, regulatory guidelines, and company Standard Operating Procedures (SOPs) as appropriate.

Depending on the location, Quality, Health, Safety, and Environment (QHSE) and Regulatory Compliance (RC) responsibilities may be included.

What You Will Do

Develop processes and procedures to maintain compliance with FDA regulations. Lead internal and external audits Monitoring current trends of regulatory agencies and deliver proactive approach to ensure inspection readiness and high quality results to Sponsors. Understanding the impact of changes on the organizations’ quality system and working with Testing Facility Management (TFM) and the Institutional Official (IO) to drive change.

Communicating regulatory updates (especially to TFM and IO). Providing vendor oversight to ensure compliance. Defining quality goals and strategic initiatives for the organization and working with TFM to achieve them. Conducting functional area review to provide TFM with assessment of organizational risk to quality. Lead FDA audits and other authorities and client audits as needed.

Manage CAPA processes and ensure timely execution of all phases. Advise other quality systems such as equipment, calibration, preventive maintenance. Oversee document control group and training requirements with timely execution. Deploy relevant training to staff. Responsible for establishing and compiling metrics related to quality system areas.

Identify and oversee continual improvement efforts.

Qualifications

Required skills

Bachelor's Degree in a science related discipline 7-10 years’ experience in health care field preferably with medical device experience Solid, demonstrable understanding of FDA regulations Highly Preferred: Experience hosting audits with major medical device manufacturers and government agencies (USDA, DEA, DOD) Experience with Master Control or similar quality system Experience with OECD regulations Veranex is an equal opportunity employer and prohibits discrimination of any kind.

All qualified applicants will receive consideration for employment without regard for race, color, religion or belief, sex (including pregnancy, gender identity or gender expression), sexual orientation, parental or marital status, disability, age, status as a protected veteran, national, social, or ethnic origin, or any other applicable legally protected characteristics.

Applicants must be currently authorized to work in the United States on a full-time basis. The company is not able to sponsor visas or provide employment-based immigration sponsorship for this role now or in the future. Protecting Your Job Search (Recruitment Scam Awareness) At Veranex, we believe our people are what set us apart, and our commitment to supporting talent begins the moment you consider joining our team.

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