Associate Director, Quality Control Compliance

BeiGene, Ltd.; Northern (KY); Hybrid; USD 134,000 - 184,000; Full time

Benefits offered by this job

Medical benefits

Dental benefits

Vision benefits

401(k)

FSA/HSA

Life Insurance

Paid Time Off

Wellness program

Equity awards

Employee Stock Purchase Plan

Job summary

BeOne Medicines Ltd. is seeking an Associate Director, Quality Control Compliance to lead QC lab compliance programs and ensure GMP/EU GMP regulatory adherence.

The role oversees investigations of OOS/OOT/OOE, documents, CAPA, and change controls, and partners with QA, Regulatory Affairs, and Manufacturing to support compliant submissions and continuous improvement. The position is based at the Hopewell, NJ site and requires strong leadership, compliance expertise, and a track record of driving

Qualifications

• BS degree and 8+ years in FDA-regulated biotech/pharma environment required.
• Master’s degree and 6+ years preferred.
• 5+ years of managerial or leadership experience directing teams or projects.
• Extensive knowledge of cGMP/EU GMP regulations for large molecule manufacturing.
• Strong leadership, mentoring, and communication skills.

Responsibilities

• Develop, implement, and maintain QC compliance programs aligned with regulatory standards and internal policies.
• Lead laboratory investigations for OOS, OOT, and OOE with regulatory compliance.
• Oversee writing of SOPs, deviation/CAPA records, and change control assessments.
• Lead internal/external GMP audits and collaborate with QA to improve QMS health.
• Mentor QC compliance staff and participate in risk assessments and CAPA planning.

Skills

Leadership

Analytical thinking

Problem solving

Effective communication

Project management

Education

Bachelor of Science

Master's degree preferred

Tools

Veeva

ThermoScientific LIMS

Job description

## Associate Director, Quality Control ComplianceApply: Hopewell: Full time: Posted Yesterday: R36949BeOne continues to grow at a rapid pace with challenging and exciting opportunities for experienced professionals. When considering candidates, we look for scientific and business professionals who are highly motivated, collaborative, and most importantly, share our passionate interest in fighting cancer.***General Description:*** The Associate Director, QC Compliance will lead and manage all activities related to Quality Control lab compliance to ensure adherence to GMP guidelines in the manufacturing and testing of large and small molecule products. This role will focus on establishing QC compliance protocols, ensuring effective quality assurance processes, and maintaining regulatory compliance with FDA/EU regulations. The Associate Director will also support the development and implementation of compliance procedures and lead investigations related to compliance deviations. This role is located at the Hopewell, NJ site. ***Essential Functions of the job:*** * Develop, implement, and maintain Quality Control compliance programs in alignment with regulatory standards and internal policies.* Lead and manage laboratory investigations for Out of Specification (OOS), Out of Trend (OOT), and Other Exceptions (OOE) results, ensuring thorough evaluation and adherence to cGMP regulations.* Oversee the preparation and technical writing of compliance-related documents, including SOPs, compliance reports, deviation and CAPA records, and change control impact assessments.* Lead the establishment of a compliance monitoring program, including participation in internal and external GMP audits to ensure laboratory adherence to industry standards.* Collaborate daily with Quality Assurance to maintain and improve the health of the quality management system.* Collaborate cross-functionally with other departments including Regulatory Affairs, Manufacturing, and Quality Assurance to facilitate successful regulatory submissions and compliance initiatives.* Champion a sustainable culture of quality, compliance, accountability, and continuous improvement across the QC organization.* Guide and mentor QC compliance and review staff to enhance their capabilities, fostering a high-performing culture and promoting professional development.* Actively participate in risk assessments and assist in developing CAPA plans to tackle any compliance issues or potential risks efficiently.* Ensure effective communication and training regarding compliance standards and regulatory expectations across the QC laboratory team. ***Core Competencies, Knowledge and Skill Requirements*** * Bachelor of Science degree and 8+ years of relevant working experience in an FDA-regulated biotechnology or pharmaceutical manufacturing environment required.* Master’s degree and 6+ years of related scientific experience preferred* 5+ years of managerial experience directly managing people and/or leadership experience leading teams, projects, programs or directing the allocation of resources.* Extensive knowledge of cGMP/EU GMP regulations and compliance, especially relating to large molecule manufacturing.* Strong leadership and team management skills, with proven capabilities in mentoring and developing staff.* Excellent analytical and problem-solving capabilities, with a track record of resolving complex compliance issues.* Highly effective communicator, both written and verbal, capable of engaging with technical and non-technical stakeholders.* Strong project and program management skills with experience directing multiple priorities within a fast-paced environment.* Attention to detail and commitment to producing quality work, with the ability to work proactively and independently. **Supervisory Responsibilities:** * Manage and mentor a dedicated team of 1-2 QC compliance professionals, including data reviewers. **Computer Skills:** * Strong PC literacy required; MS Office skills (Outlook, Word, Excel, PowerPoint)* Experience with Veeva and ThermoScientific LIMS is a plus **Travel:** * Must be willing to travel approximately 20%* Ability to work on a computer for extended periods of time Global CompetenciesWhen we exhibit our values of Patients First, Driving Excellence, Bold Ingenuity and Collaborative Spirit, through our twelve global competencies below, we help get more affordable medicines to more patients around the world.* Fosters Teamwork* Provides and Solicits Honest and Actionable Feedback* Self-Awareness* Acts Inclusively* Demonstrates Initiative* Entrepreneurial Mindset* Continuous Learning* Embraces Change* Results-Oriented* Analytical Thinking/Data Analysis* Financial Excellence* Communicates with ClaritySalary Range: $133,800.00 - $183,800.00 annuallyBeOne is committed to fair and equitable compensation practices. Actual compensation packages are determined by several factors that are unique to each candidate, including but not limited to job-related skills, depth of experience, certifications, relevant education or training, and specific work location. Packages may vary by location due to differences in the cost of labor. The recruiter can share more about the specific salary range for a preferred location during the hiring process. Please note that the listed range reflects the base salary or hourly range only. Non-Commercial roles are eligible to participate in the annual bonus plan, and Commercial roles are eligible to participate in an incentive compensation plan. All Company employees have the opportunity to own shares of BeOne Medicines Ltd. stock because all employees are eligible for discretionary equity awards and to voluntarily participate in the Employee Stock Purchase Plan. The Company has a comprehensive benefits package that includes Medical, Dental, Vision, 401(k), FSA/HSA, Life Insurance, Paid Time Off, and Wellness.We are proud to be an equal opportunity employer. BeOne does not discriminate on the basis of race, religion, color, sex, gender identity, sexual orientation, age, disability, national origin, veteran status or any other basis covered by appropriate law. All employment is decided on the basis of qualifications, merit, and business need. In order to ensure reasonable accommodation for individuals protected by Section 503 of the Rehabilitation Act of 1973, the Vietnam Era Veterans’ Readjustment Assistance Act of 1974, Title I of the Americans with Disabilities Act of 1990, and any other applicable federal, state or local laws, applicants who require reasonable accommodation in the job application process may contact [e-mail].