Director, Quality Control

Job Description:As a privately-owned, biopharmaceutical company, Ferring pioneers and delivers life-changing therapies that help people build families and live better lives. Our independence helps us cultivate an entrepreneurial spirit and long-term perspective that enables us to achieve growth and scale, while remaining agile and true to our ‘people first’ philosophy. Built on a 70-year plus commitment to science and research, Ferring is relentless in its pursuit of science that drives powerful discoveries and therapies to help people build families, stay healthy, and stand up to the world’s oldest enemy: disease. As Director, Quality Control you will be responsible for strategic leadership and oversight of the Quality Control (Analytical and Microbiology) function, including testing at contract labs for drug substance, drug product, and stability programs across commercial and development portfolios. Partner cross-functionally with Pharmaceutical Development, Technical Operations, QA, and CMC Regulatory Affairs to manage method transfers, validations, and data oversight aligned with development and production timelines. Key responsibilities include vendor oversight, data review, external audits, and management of GMP-related exceptions (e.g., deviations, CAPAs, OOS/OOT, change controls).Oversees designation of critical quality attributes, specification setting, and trending of method and product performance. Provides direction on method transfers and validations, ensuring compliance with regulatory standards and laboratory control requirements.With Ferring, you will be joining a recognized leader, identified as one of “The World’s Most Innovative Companies” by Fast Company, and honored by Fortune with inclusion on its “Change the World List,” for addressing society’s unmet needs. Ferring US is also Great Places to Work Certified, distinguishing it as one of the best companies to work for in the country. Responsibilities: Leadership & StrategyProvide strategic direction for the Quality Control department to achieve corporate and site-level objectives.Build and lead high-performing team.Coach, mentor, and engage team to ensure business goals and development plans are met.Manufacturing & Quality Control ResponsibilitiesOversee manufacturing unit operations, including review and approval of preventive maintenance activities and changes.Review and approve issues and investigations related to critical equipment, systems, and utilities.Establish and monitor operational metrics to track performance and identify trends.Quality Oversight & ComplianceDevelop and implement short- and long-term plans to ensure corporate and operational compliance with GxP standards.Ensure deployment and maintenance of quality processes aligned with regulatory requirements and internal policies.Manage planning and budgeting for Quality Control activities.Third-Party OversightEnsure third-party labs and CMOs comply with quality standards and regulatory expectations to meet product quality attributes.Provide QC oversight and approval of cGMP documentation (e.g., change controls, deviations, CAPAs, SOPs, validation protocols).Quality Systems & Continuous ImprovementLead or support QC-related projects and propose improvements using risk-based approaches.Maintain robust training programs to meet GMP and company requirements.Coordinate lab activities and actively participate in regulatory inspections, third-party audits, and customer audits.Regulatory Awareness & Strategic ResponseMonitor emerging regulatory requirements and assess organizational impact.Lead remediation efforts for identified gaps and drive continuous improvement initiatives.Performs other duties / projects as assigned by the Vice President, Technical Operations.Requirements: Education & Experience: Bachelor’s degree in a scientific discipline with 15+ years of experience in pharmaceutical QC operations across development and commercial stages. Alternatively, a Master’s degree with 12+ years or a PhD with 10+ years is acceptable. Small molecule experience is required; biologics experience is highly preferred.Technical Expertise: Strong background in analytical and microbiological method development, validation, transfer, and continuous improvement. Advanced knowledge of GMP testing oversight at CMOs, including laboratory and stability functions.Regulatory & Compliance: Proven success managing FDA and global regulatory inspections, vendor audits, and addressing inspectional findings. Deep understanding of GMPs, regulatory expectations, and the pharmaceutical development lifecycle, including process and method transfer from development to commercialization.Quality Systems: Broad knowledge of risk-based quality systems and key elements such as complaints, change control, APR/PQR, and compliance-related events. Proficient in MS Office, Trackwise, Oracle, Empower, and LIMS.Leadership & Strategy: Demonstrated ability to build and lead high-performing teams, develop strategic quality objectives, and drive process improvements. Skilled in coaching, mentoring, and stakeholder education.Communication & Influence: Excellent interpersonal, negotiation, and influencing skills with the ability to manage multiple priorities and lead change across all organizational levels.Cross-Functional Collaboration: Effective in partnering across departments to enhance Quality Management Systems and align resources to achieve shared goals.Physical Requirements: Frequent standing and walking across manufacturing, laboratory, and office areasMay involve stooping, bending, crouching, and kneelingMay involve handling of samples, packaging, or small equipment, up to 25–50 lbs.Work typically occurs in cGMP-controlled lab and plant environment, often requiring personal protective equipment (PPE) such as lab coats, gloves, eye protection, and occasionally respirators.May involve exposure to cleanroom conditions, chemicals, or fluctuating temperatures due to lab or plant protocols. Ferring + you At Ferring, we offer competitive total compensation along with an exceptional range of flexible benefits, personal support and tailored learning and development opportunities all designed to help you realize your full potential both in life and at work. From working hours that respect your lifestyle, a culture that is welcoming and equitable, and the chance to work with the industry’s most impressive people, these are just some of the ways we live our "People First" philosophy. Our Compensation and Benefits At Ferring, base salary is one part of our competitive total compensation and benefits package and is determined using a salary range. The base salary range for this role is $158,136 to $194,472, which is the reasonable estimate of the base compensation for this role. The actual amount paid may differ based on non-discriminatory factors such as experience, knowledge, skills, abilities, education and primary work location. Additional compensation for this role will be provided based on competitive annual incentive compensation targets in the form of an annual bonus - payouts are based on individual and company performance. Benefits for this role include comprehensive healthcare (medical, dental, and vision) with a premium differential, inverse to base salary, to be paid by employees, a 401k plan and company match, short and long-term disability coverage, basic life insurance, wellness benefits, reimbursement for certain tuition expenses, sick time of 1 hour per 30 hours worked, vacation time for full time employees to accrue up to 120 hours in the first four (4) years of employment, and 160 hours in the fifth (5th) year of employment as well as 15 paid holidays per year. We are proud to offer paid parental leave subject to a minimum period of employment at Ferring. Ferring is an equal opportunity employer. All aspects of employment will be based on merit, competence, performance, and business needs. We do not discriminate on the basis of race, color, religion, marital status, age, national origin, ancestry, physical or mental disability, medical condition, pregnancy, genetic information, gender, sexual orientation, gender identity or expression, veteran status, or any other status protected under federal, state, or local laws. Join our team and your voice will be heard, and your contributions will be valued. If you love to come up with new ways to make a positive difference and see them through, you will fit right in. We are proud to be an Affirmative Action/Equal Opportunity Employer (including Disability/Protected Veterans). We maintain a drug-free workplace. Location:Parsippany, New JerseySummaryLocation: Parsippany, New Jersey, United StatesType: Full time