Executive Director, Quality Control

Revance; Town of Newark (WI); On-site; USD 200,000 - 260,000; Full time

Benefits offered by this job

Competitive compensation

Annual bonus

Flexible PTO

Healthcare benefits

HSA match

401k match

Life and disability insurance

Job summary

Revance is seeking an Executive Director of Quality Control to lead QC across development through commercialization of clinical and commercial products globally. The role drives phase-appropriate analytical development and ensures compliance with GxP regulations and quality systems.

Responsibilities include overseeing QC/analytical/microbiology, interaction with FDA/EMA, and budget/people leadership to advance programs from development to registration and post-approval improvements.

Qualifications

• Global GxP regulatory experience is required across development, manufacturing, and QA.
• Proven senior leadership experience in biopharma or biotech environments.
• Demonstrated excellence in oral and written communication with regulators and teams.
• Experience budgeting and planning resources to meet department objectives.
• Strong track record in promoting quality systems and regulatory approvals in biotech/pharma.

Responsibilities

• Serve as QC liaison to US FDA and external agencies.
• Develop resourcing strategies and budget for the department.
• Establish and improve QC processes for microbiology and analytics labs.
• Provide strategic direction for QC analytical and microbiology functions.
• Oversee GMP, GLP, GCP and GDP compliance across operations.
• Lead regulatory submissions support and interactions with regulators.

Skills

Global GxP regulatory experience

Senior leadership

Excellent communication skills

Budgeting and resource planning

Biopharma/biotech industry expertise

Education

Bachelor of Science in sciences/engineering

PhD in biochemistry/chemistry/pharmaceutical sciences

Tools

JMP software

Job description

Job Summary:

The Executive Director of Quality Control will be responsible for all aspects of quality control from drug development through commercialization, including the manufacture of clinical products, conduct of clinical trials, oversight of GCP and GLP CROs, and the manufacture/distribution of commercial products globally. This role will also be responsible for leading science-driven, phase appropriate analytical development to support clinical programs to commercial registration and post approval improvements both internally and at third party contractors

This position is a broad-based, strategic position requiring a true quality approach to assessing data and problem solving in accordance with applicable global Gx P regulations.

Essential Duties:

• Serve as the primary Quality Control (QC)Analytical and Microbiology liaison of the company to US FDA and external US agencies and ensure Revance is appropriately represented in QC matters.
• Develop resourcing strategies, allocate budget for department to meet company objectives and efficient operations
• Establish, maintain and improve all processes within the Microbiology and Analytical Laboratories for both internal and externally tested biological products. QC Accountability may extend to other GxP regulated products within Revance (Rx, OTC, medical devices).
• Provide strategic direction for QC analytical and microbiology functions, including environmental monitoring.
• Oversee quality control operations to assure compliance with quality systems, data integrity requirements, and all applicable regulations.
• Provide guidance for phase appropriate in-process, release, and shelf-life specification establishment and lead review/approval in compliance with applicable global guidance and regulations.
• Co-lead with analytical development the development, validation, deployment and management of analytical methods ensuring compliance with applicable ICH guidelines and global regulations.
• Oversee drug substance, bulk drug product, and finished product manufacturing and packaging, QC release and stability testing, and final lot disposition.
• Ensure adherence to GMPs, GLPs, GCPs and GDPs.
• Interact regularly with contract manufacturers and contract testing laboratories.
• Establish and adhere to all quality agreements.
• Provide support for regulatory submissions.
• Manage regulatory agencies (FDA, EMA), and state board health inspections.
• Provide quality support for adverse events and complaints.
• Chair Senior Management review of quality control metrics.
• Build, coach, mentor and ensure appropriate management development for key personnel in his/her department

EDUCATION

Minimum required:

• Bachelor of Science degree in sciences/engineering with at least 15 years of related experience

OR:

• D. in relevant scientific discipline such as biochemistry, chemistry, pharmaceutical sciences or related field with at least 5 years of related experience.

EXPERIENCE

• 15+ years of progressive experience in the biotechnology or pharmaceutical industry.
• 5+ years in related field at a senior level and leadership position.

KNOWLEDGE, SKILLS AND ABILITIES

Minimum required:

• Global GxP regulatory experience.
• Respected senior development executive in the bio-pharmaceutical field
• Have a strong record of accomplishment in quality, as demonstrated by successful regulatory approvals of drug candidates under his/her responsibility during development.
• Be able to develop/communicate a compelling vision/ sense of purpose for the function/organization and work collaboratively to formulate long-range and mid-term strategies.
• Possess excellent oral and written communication skills.
• Be a self-confident, proactive, influential and decisive leader who has the talent to engage other company managers and external affiliations in productive collaborations.
• Experience developing and organizing a budget.
• Broad experience in analytical sciences supporting late stage and commercial products.
• Strong strategic sense and communication skills with authorities.
• Proven track record with a number of successful marketing applications.
• Experience in development of biological assays.
• Working knowledge of statistics.

Preferred:

• Experience with JMP statistical software
• Experience with cell-based potency assays

Company Summary:

Revance is a global company developing, producing, and distributing industry-leading, differentiated products across aesthetics, skincare, and therapeutics. Revance drives innovation beyond convention to offer treatment options for individuals across generations. The Company’s vision is to redefine excellence in aesthetics, skincare, and therapeutics through science-powered innovation, with an unwavering commitment to its providers, patients, and consumers. Revance’s award-winning products are the result of robust research and development, a cornerstone for the Company, driven by renowned scientists. For more information about Revance, please visit us at www.revance.com.

What Revance invests in you:

• Competitive Compensation including base salary and annual performance bonus.
• Flexible PTO, holidays, and parental leave.
• Generous healthcare benefits, HSA match, 401k match, employer paid life and disability insurance, pet insurance, wellness discounts and much more!

This section of the job description is required by the American with Disability Act (ADA). The ADA requires that job descriptions reflect the physical and mental demands required to effectively perform the essential duties of the job. The ADA prohibits employers from discriminating against a “qualified individual with a disability” in all aspects of the employment relationship. A “qualified individual with a disability” is “an individual who meets the education, experience, skill, and other job-related requirements of a position held or desired, and who, with reasonable accommodation, can perform the essential functions of a specified job.”

Revance is an Equal Opportunity employer. All qualified applicants will receive consideration for employment based on merit, without regard to race, color, religion, sex, national origin, disability, protected Veteran Status, or any other characteristic protected by applicable federal, state, or local law.