Sr. Quality and Regulatory Affairs Manager

Ready to make an impact?

We develop, manufacture, and supply dental implants, clear aligners, instruments, CADCAM prosthetics and biomaterials for use in esthetic dentistry, tooth replacement and restoration solutions or to prevent tooth loss.

We empower our employees to perform and make an impact, to question the status quo, to drive change, to stay ahead of the competition. From the first Dental Implant in 1974 to the latest Digital Solution – we do things differently than others

We deliver innovation based on evidence. This is part of our employer culture as well as an exceptional team spirit that truly encourages diversity and a powerful “can-do” attitude.

Salary: $138, 000.00 /145, 500.00 Annually. The final pay for this position will vary based on geographic location and candidate experience relative to what the company reasonably anticipates for this position.

LOCATION: Femont, California

Summary of Position:

Bay Materials strives to be the best provider of materials used for fabricating devices and treatments in the dental and orthodontic industry. This position is responsible for overseeing the company Quality Management and Regulatory Affairs activities and processes for products marketed in current and future markets, and for ensuring compliance to all applicable Quality System Regulations, including ISO 13485 and any other applicable quality and regulatory requirements for design and manufacturing. This role will evolve along with the company QMS as the company develops and commercializes new products and gains approval to market in various geographic markets.

Essential Functions and Duties:

Quality Management

• Maintains the company Quality Management System to meet all applicable requirements for design & development, manufacturing and distribution for all Bay Materials products
• Drives continuous improvement projects including the development of improved Quality Systems processes
• Manages Quality personnel(s) which may include individuals whose functions include Quality Engineering, Document Control, Incoming Inspection, Quality Assurance Testing, Calibration, Validation, and other related responsibilities
• Maintains a thorough understanding of medical device quality system requirements such as ISO 13485
• Ensures required quality procedures are established including CAPA, Non-Conforming Product, Risk Management, Post-market-surveillance, Purchasing Controls, Management Review, Traceability, Employee Controls, Post market management, Change Control, Advisory Notifications, Supplier compliance and others as coordinated within the Quality team and with other cross-functional departments
• Ensures the company internal audit schedule is managed in accordance with existing procedures.
• Coordinates and prepares site audit from health authority, notified bodies, and key customers.
• Ensure quality compliance is well established at supplier especially for critical suppliers
• Develops and conducts training on key quality topics and best practices including Root Cause Investigations, CAPA investigations, Management Responsibility, GMP/GDP, Audit Readiness, and Validation
• manages internal processes and metrics are aligned to create highest product quality to achieve business objectives.
• Collaborates with Research & Development and Manufacturing organizations to ensure compliance is met and maintained.
• Follows safety rules and maintains personal safety and the safety of others, including maintaining a clean and safe work area
• Accurately records and reports information as required
• Ensure product release according to defined specifications
• Be site management representative

Regulatory Affairs

• Assess regulatory requirements and guidelines for countries in which Bay Materials markets and sells its products.
• Ensure that all applicable regulatory documentation requirements are met for each country.
• Coordinate and organize test data and clinical or scientific reviews in support of regulatory submissions
• Communicate with regulatory agencies and reviewers to ask or answer questions
• Ensure compliance with product labeling and packaging requirements
• Coordinate work or projects with 3rd party testing or consulting services
• Prepare for and lead ISO audits and certifications, or other accreditation efforts
• Prepare for and support internal and external audits
• Review and revise regulatory documents related to company products
• Review and approve all sales and marketing materials to ensure compliance with applicable regulatory requirements

Non-essential Functions and Duties:

• Perform other related duties and responsibilities as assigned

Management Responsibilities:

This position manages the following positions:

• Manages Quality personnel(s) which may include individuals whose functions include Quality Engineering, Document Control, Incoming Inspection, Quality Assurance Testing, Calibration, Validation, and other related responsibilities
• Manage and lead diverse teams from different cultural backgrounds
• Foster an inclusive work environment that respects and leverages cultural differences
• Provide training and development programs to enhance cross-cultural competencies within the organization

Minimum Qualifications:

• Bachelor’s degree in chemistry, biology, engineering, technology, or related science
• 8+ years relevant experience in quality control, quality assurance, and regulatory affairs at a Class I or Class II medical device manufacturer
• 8+ years experience formal ISO 13485 Lead Auditor training or agree to successfully complete such training within the first 6 months of employment
• 8+ years of experience utilizing the basic quality tools including RCA, Fishbone analysis, SPCs, checklists, histograms, Pareto, scatter diagrams, process mapping and flow charts
• 8+ years of experience producing technical documents, such as draft management review, KPIs at defined timeline, risk management for the quality system and formal procedures/ work instructions

Preferred Qualifications:

• Masters degree in chemistry, biology, engineering, technology, or related science preferred
• Familiarity with GDP (Good Documentation Practices)
• Familiarity with and competency in Document and Record Control including 21 CFR Part 11 Compliance
• Familiarity with U.S. and International medical device regulations
• Excellent interpersonal, verbal, and written communication skills
• Basic computer skills, including Microsoft Office Suite

Whether you’re looking to build your career, improve your health, or brighten your SMILE, we offer generous benefits to help you achieve your goals.

• Very Competitive total compensation plans 90% Employer Paid!

• A 401(K) plan to help you plan for your future with an employer match

• Great health, dental and vision insurance packages to fit your needs to ensure you’re happy and healthy. Straumann contributes a healthy portion towards employees’ premium.

• Generous PTO allowance - plenty of time to recharge those batteries!

Please understand that we do not need external support by recruiting agencies and consultants to fill this vacancy. Thank you for respecting this.

Videos To Watch

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