Compliance Specialist Lead

Forge Biologics
Columbus, OH
On-site

Who this role is best for

A natural match if you have experience in GMP compliance and managing internal audit processes.

Best fit for

  • Candidates with GMP compliance leadership experience in biologics or pharmaceutical manufacturing
    — “compliance experience in a regulated industry (i.e., regulatory compliance experience in a pharmaceutical, biotech, or biologics GMP regulated manufacturing environment)”
  • Professionals who can drive quality culture and ensure audit readiness across teams
    — “Exemplifies good quality and compliance practices while championing Quality Culture throughout the organization.”
  • Individuals comfortable with cross-functional collaboration and regulatory agency engagement
    — “Partner with internal departments (e.g. Manufacturing, Quality, Facilities and Engineering) to ensure end-to-end compliance throughout the product lifecycle and commercial readiness.”

Things to consider

  • The role demands a high level of attention to detail and documentation review
    — “Track corrective actions as a result of audit observations and obtains and reviews objective evidence”
  • Candidates should be prepared for potential on-site work and PPE usage
    — “When on-site, adherence to safety requirements and use of PPE may be necessary.”

How to stand out

  • Highlight experience in managing audit processes and ensuring compliance outcomes
    — “Ownership of the Internal Audit process, planning, execution and verification of actions.”
  • Emphasize your ability to coordinate cross-functional teams for compliance
    — “Partner with internal departments (e.g. Manufacturing, Quality, Facilities and Engineering) to ensure end-to-end compliance”
  • Showcase your knowledge of GMP standards and their application in regulated environments
    — “Working knowledge of quality systems and ability to apply GMP’s in conformance to U.S. and Global standards”
  • Demonstrate experience with external audits and regulatory agency interactions
    — “Experience interacting with domestic and international regulatory agencies.”
Pace · SteadyCollaboration · HighAutonomy · MediumDecision Impact · Team

Derived from job-description analysis by Serendipath's career intelligence engine.

What success looks like

  • oversaw the Internal Audit process
  • supported Regulatory Compliance/Quality Representatives
Typical background
5+ years of compliance experience

Skills & requirements

Required

Regulatory ComplianceQuality ManagementInternal AuditGMP ComplianceQuality System MonitoringCross-functional Collaboration

Preferred

Experience In Gene Therapy ManufacturingCgmp Facility Operations

Stack & domain

Regulatory ComplianceQuality ManagementInternal AuditGMPQuality SystemRisk ManagementTrainingSopsLeadershipCollaborationQuality CultureProcess ImprovementStakeholder ManagementComplianceBiologicsGene TherapyManufacturingRegulatory AffairsQuality Assurance

About the role

Original posting from Forge Biologics via Greenhouse

Forge Your Future with Us: 

At Forge Biologics, we believe in turning bold ideas into life-changing realities. Our mission is simple yet powerful: to enable access to life-changing gene therapies and help bring them from ideas into reality. We partner with scientists, physicians, biotech and pharma innovators, and patient communities — all united by one goal: improving lives. If you’re driven by purpose and excited to make a tangible impact, this is where your journey begins. 

Our team works out of The Hearth, a state-of-the-art, 200,000-square-foot cGMP facility in Columbus, Ohio. Here, you won’t just watch innovation happen — you’ll be part of it. Whether you’re scaling AAV manufacturing, collaborating on cutting-edge therapies, or supporting complex technical projects, you’ll play a key role in bringing hope to patients with genetic diseases. 

What sets Forge apart is our culture of H.O.P.E. We are hardworking, showing up each day with determination and grit. We are open, creating a space where ideas flow freely and every voice is valued. We are purpose-driven, with every task directly tied to changing lives. And we are engaged, energized by the challenges we face and the milestones we achieve together. 

At Forge, your growth matters. We’re committed to helping you expand your skills, take on new challenges, and develop your career through mentorship, hands-on learning, and opportunities for advancement. Our people are our greatest investment, and we’re proud to see team members grow with us. 

If you’re ready to use your talent to help deliver hope to patients around the world, join us — and be part of something bigger than yourself. 

About The Role:   

We are currently seeking a Compliance Specialist Lead, to join the Forge Biologics team. This position will drive both the strategy and the delivery for Regulatory and Quality Compliance Initiatives, and this individual also oversees the GMP Internal Audit program. This person will support improvement initiatives related to the Quality Management Review (QMR), and support External Audit program, and processes to ensure Forge’s compliance with the appropriate regulatory agency requirements, internal company standards, client requirements, and current Good Manufacturing Practices (cGMPs).  

Responsibilities: 

Ownership of the Internal Audit process, planning, execution and verification of actions. 

Support Regulatory Compliance/Quality Representatives and apply regulatory knowledge and judgment to identify potential compliance concerns and identify potential remediation action. 

Track corrective actions as a result of audit observations and obtains and reviews objective evidence as actions are completed in accordance with prescribed commitments.  

Support and update Site Governance and Standard Operating Procedures, Training and content/delivery. Promote audit/ inspection ready culture. 

Support the coordination of Management Review includes monitoring the overall health of the Quality system through evaluation of KPIs, effectiveness checks, and risk management.  

Partner with internal departments (e.g. Manufacturing, Quality, Facilities and Engineering) to ensure end-to-end compliance throughout the product lifecycle and commercial readiness. 

Exemplifies good quality and compliance practices while championing Quality Culture throughout the organization.  

Qualifications: 

Bachelor’s degree in related discipline with 5+ years of compliance experience in a regulated industry (i.e., regulatory compliance experience in a pharmaceutical, biotech, or biologics GMP regulated manufacturing environment).  

Excellent analytical, communication, and problem solving skills  

Proven ability to manage multiple prior in a fast- paced environment. 

Experience interacting with domestic and international regulatory agencies. 

Working knowledge of quality systems and ability to apply GMP’s in conformance to U.S. and Global standards, and where appropriate, other regulatory authority standards.  

Partner with internal departments (e.g. Manufacturing, Quality, Facilities and Engineering) to ensure end-to-end compliance throughout the product lifecycle and commercial readiness. 

Exemplifies good quality and compliance practices while championing Quality Culture throughout the organization.  

Preferred Skills: 

American Society for Quality- CQA or equivalent certification 

Project or Program Management experience a plus 

Work Environment and Physical Demands   

Primarily office-based with extended computer use. Regular interaction with internal teams and external stakeholders. When on-site, adherence to safety requirements and use of PPE may be necessary. 

Position requires prolonged sitting, reviewing detailed documentation, occasional standing/walking during site audits, and the ability to lift up to 15 pounds (e.g., files or laptop equipment).  

Forge Biologics is an equal opportunity employer dedicated to building an inclusive and diverse workforce. Forge Biologics, provides equal employment opportunities to all employees and applicants for employment and prohibits discrimination and harassment of any type without regard to race, color, religion, age, sex, national origin, disability status, genetics, protected veteran status, sexual orientation, gender identity or expression, or any other characteristic protected by federal, state or local laws.  

We’ve Got You Covered:

At Forge Biologics, we believe our people deserve to be taken care of – in and out of the workplace. We’ve built a comprehensive compensation and benefits package designed to help you thrive, grow, and feel valued every step of the way:

Health from day one

Health, dental and vision insurance start your first day – with 90% of premiums covered for you and your family.

Time to recharge

A competitive paid time off plan – because rest fuels innovation.

12 weeks of fully paid parental leave so you can focus on family when it matters most.

Rewarding your impact

Annual bonus opportunities for all full-time team members.

401(k) with company match to help you plan for the future.

Special employee discounts, including childcare and dependent care savings.

Your wellness, supported

Onsite fitness facility at The Hearth.

Mental health counseling and financial planning services through our Employee Assistance Program.

Employer-paid short and long-term disability coverage to protect your peace of mind.

Fuel for your workday

A fully stocked kitchen with free snacks and beverages – we keep you energized and ready for what’s next.

Grow with us

Ongoing professional development resources, training, and mentorship programs to help you build your care and grow within Forge.

Source: Forge Biologics careers (Greenhouse)

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