Sr. Manager, Quality Compliance

Overview

As a privately-owned, biopharmaceutical company, Ferring pioneers and delivers life-changing therapies that help people build families and live better lives. Our independence fosters an entrepreneurial spirit and long-term perspective to achieve growth and scale while remaining agile and true to our ‘people first’ philosophy. With a 70-year commitment to science and research, Ferring pursues science that drives discoveries and therapies to help people build families, stay healthy, and stand up to disease.

Join our dynamic Quality Operations team as a Senior Manager, Quality Compliance
, where you’ll play a critical role in safeguarding product integrity and patient safety. This position suits a strategic thinker who thrives in a fast-paced environment and is passionate about driving excellence in compliance. You will lead initiatives that ensure regulatory adherence, strengthen quality systems, and prepare the organization for inspections—collaborating across functions to influence business outcomes.

• Lead with Impact:
  Drive internal audit programs, inspection readiness, and compliance initiatives that shape our quality culture.
• Be a Trusted Expert:
  Provide guidance on GMP, GDP, DSCSA, and FDA expectations to cross-functional teams.
• Own Compliance Strategy:
  Develop and refine SOPs, policies, and quality documentation to meet evolving regulatory requirements.
• Analyze & Improve:
  Monitor Quality Compliance KPIs, identify trends, and implement continuous improvement strategies.
• Champion Regulatory Excellence:
  Host and support FDA and third-party inspections, ensuring flawless execution.
• Manage Critical Processes:
  Oversee U.S. recall activities, FAR, BPDR, and FDA communications.
• Collaborate for Success:
  Partner with teams on DSCSA compliance, serialization, and suspect product investigations.

• Education:
  
  Bachelor’s degree in Life Sciences, Pharmaceutical Sciences, or related field.
• Experience:
  
  Minimum 4 years in pharmaceutical or biopharmaceutical Quality, Compliance, Regulatory or related roles.
• Expertise:
  Strong knowledge of GMP, GDP, GVP, DSCSA, and FDA regulations; proven auditing experience (ASQ CQA, ISO Lead Auditor, Veeva, Trackwise or equivalent);
  Microsoft Suite knowledge.
• Skills:
  
  Ability to influence without authority, manage complex compliance processes, and travel up to 20%.

• GVP auditing experience.

• Strategic Agility
• Collaboration & Influence
• Risk-Based Thinking
• Communication Excellence
• Continuous Improvement Mindset
• Ethics & Integrity

At Ferring, we offer competitive total compensation along with an exceptional range of flexible benefits, personal support and tailored learning and development opportunities. Our culture is welcoming and equitable, guided by a strong People First philosophy. We provide flexible working hours and opportunities to work with industry-leading colleagues.

Base salary for this role ranges from $144,000 to $166,000, with actual pay determined by experience, knowledge, skills, abilities, education, and location. Additional compensation may include an annual incentive bonus based on individual and company performance. Benefits include comprehensive healthcare (medical, dental, and vision) with a premium differential, a 401k plan with company match, disability coverage, life insurance, wellness benefits, tuition reimbursement, paid time off, holidays, and paid parental leave subject to eligibility.

Ferring is an equal opportunity employer. All employment decisions are based on merit and business needs, without discrimination. We are proud to be an Affirmative Action/Equal Opportunity Employer (including Disability/Protected Veterans) and maintain a drug-free workplace.

Parsippany, New Jersey