Committed to the preservation of vision.
Help bring the first ophthalmic formulation of bevacizumab to people living with wet AMD.
Director, Quality Systems and GxP Compliance
Outlook Therapeutics (Nasdaq: OTLK) is a commercial-stage biopharmaceutical company redefining the standard of care in retinal disease. In the United States, our lead product has received FDA approval, making it the first and only FDA-approved ophthalmic formulation of its kind for the treatment of wet AMD, and we are preparing for US commercial launch. Our lead product is also the first ophthalmic formulation of its kind to receive Marketing Authorization from the European Commission and the UK MHRA for the treatment of wet age-related macular degeneration (wet AMD), and has launched across Germany, Austria, and the UK. Driven by the stories of the patients we serve, we are united with the vision-care community around a single goal: a future where everyone with retinal disease can envision a brighter world.
THE OPPORTUNITY
Reports To - VP, Quality Assurance
Level - Director
Location - Remote (US-based) with global scope
Employment Type - Full-time
Direct Reports - No
This is a rare ground-floor moment at a company hitting its commercial inflection point. As a lean, fast-moving organization, we offer scope and ownership that larger companies can't: your work is visible, your decisions matter, and you'll help build the function rather than simply maintain it. You'll partner directly with senior leadership and see a clear line between what you do and patients gaining access to a new treatment option.
You'll build and run the quality systems backbone for a company scaling its Quality Management System across the US, EU, UK, MENA, LATAM, and APAC — with direct visibility into inspection readiness as we grow toward global commercial maturity.
WHAT YOU'LL DO
Quality Systems & Governance
* Lead Quality Systems and GxP Compliance operations, including Document Control, Change Control, Deviations, CAPA, and Product Complaint support.
* Build and maintain quality programs and the internal Quality Management System.
* Lead the Change Control Review Board and Quality Council.
* Drive continuous improvement across vendor and internal quality systems, incorporating outcomes from Quality Management Review activities.
Vendor & Quality Agreement Management
* Manage external oversight of GxP vendor quality systems.
* Author, maintain, and approve Quality Agreements with GxP vendors.
Audits & Inspection Readiness
* Lead internal and external GxP audit programs.
* Oversee inspection readiness activities, including mock audits and SME preparation.
* Drive timely and effective CAPA completion across the organization.
Investigations, Documentation & Regulatory Compliance
* Review and approve OOS investigations, deviations, and product complaint investigations.
* Write, review, approve, and maintain GxP SOPs and GxP policies.
* Ensure proper execution of required regulatory reporting and drug shortage notifications.
* Lead participation in Annual Product Quality Review activities.
* Ensure Quality System compliance for combination products
Cross-Functional Partnership & Team Enablement
* Provide backup QA support for batch record review and release, and for PPQ and analytical method validation reviews.
* Provide quality and GxP compliance guidance to cross-functional partners across Regulatory, Technical Operations, and Commercial.
* Ensure GxP employees complete required training.
* Represent QA in internal and external meetings.
WHAT YOU'LL BRING
Required
* Bachelor's degree in a life-science or related field.
* 10+ years of experience in biopharmaceutical or pharmaceutical Quality.
* Strong knowledge of domestic and international GMP regulations.
* Proven experience building and maintaining Quality Systems.
* Experience partnering with multi-disciplinary teams across Regulatory, Technical Operations, and Commercial.
* Strong organizational and communication skills, with the ability to resolve challenges independently.
Preferred
* Experience with electronic quality systems such as Veeva, TrackWise, or MasterControl.
* Experience supporting Quality System compliance for combination products.
* Experience operating in a global, multi-region regulatory environment (US, EU, UK, MENA, LATAM, APAC).
WHAT WE OFFER
* Competitive base salary, annual performance bonus, and equity — so you share in the value you help create
* Comprehensive health coverage: medical, dental, and vision
* 401(k) with company match
* Generous paid time off and company holidays
* A high-trust, low-bureaucracy culture with direct access to leadership and real room to grow
* Mission-driven work that helps preserve sight for patients who are counting on it
COMPENSATION
In keeping with our commitment to pay transparency, the good-faith base salary range for this role is $180,000-$220,000, with an annual target bonus of 20%. This role is also eligible for a meaningful equity grant, reflecting the opportunity to build lasting value at a company at a commercial inflection point. Final compensation reflects experience, skills, and location.
OUR COMMITMENT
Outlook Therapeutics is an equal opportunity employer. We are committed to building an inclusive environment where every team member can do their best work, and we consider all qualified applicants without regard to race, color, religion, sex, sexual orientation, gender identity, national origin, age, disability, veteran status, or any other characteristic protected by law. #J-18808-Ljbffr
Help bring the first ophthalmic formulation of bevacizumab to people living with wet AMD.
Director, Quality Systems and GxP Compliance
Outlook Therapeutics (Nasdaq: OTLK) is a commercial-stage biopharmaceutical company redefining the standard of care in retinal disease. In the United States, our lead product has received FDA approval, making it the first and only FDA-approved ophthalmic formulation of its kind for the treatment of wet AMD, and we are preparing for US commercial launch. Our lead product is also the first ophthalmic formulation of its kind to receive Marketing Authorization from the European Commission and the UK MHRA for the treatment of wet age-related macular degeneration (wet AMD), and has launched across Germany, Austria, and the UK. Driven by the stories of the patients we serve, we are united with the vision-care community around a single goal: a future where everyone with retinal disease can envision a brighter world.
THE OPPORTUNITY
Reports To - VP, Quality Assurance
Level - Director
Location - Remote (US-based) with global scope
Employment Type - Full-time
Direct Reports - No
This is a rare ground-floor moment at a company hitting its commercial inflection point. As a lean, fast-moving organization, we offer scope and ownership that larger companies can't: your work is visible, your decisions matter, and you'll help build the function rather than simply maintain it. You'll partner directly with senior leadership and see a clear line between what you do and patients gaining access to a new treatment option.
You'll build and run the quality systems backbone for a company scaling its Quality Management System across the US, EU, UK, MENA, LATAM, and APAC — with direct visibility into inspection readiness as we grow toward global commercial maturity.
WHAT YOU'LL DO
Quality Systems & Governance
* Lead Quality Systems and GxP Compliance operations, including Document Control, Change Control, Deviations, CAPA, and Product Complaint support.
* Build and maintain quality programs and the internal Quality Management System.
* Lead the Change Control Review Board and Quality Council.
* Drive continuous improvement across vendor and internal quality systems, incorporating outcomes from Quality Management Review activities.
Vendor & Quality Agreement Management
* Manage external oversight of GxP vendor quality systems.
* Author, maintain, and approve Quality Agreements with GxP vendors.
Audits & Inspection Readiness
* Lead internal and external GxP audit programs.
* Oversee inspection readiness activities, including mock audits and SME preparation.
* Drive timely and effective CAPA completion across the organization.
Investigations, Documentation & Regulatory Compliance
* Review and approve OOS investigations, deviations, and product complaint investigations.
* Write, review, approve, and maintain GxP SOPs and GxP policies.
* Ensure proper execution of required regulatory reporting and drug shortage notifications.
* Lead participation in Annual Product Quality Review activities.
* Ensure Quality System compliance for combination products
Cross-Functional Partnership & Team Enablement
* Provide backup QA support for batch record review and release, and for PPQ and analytical method validation reviews.
* Provide quality and GxP compliance guidance to cross-functional partners across Regulatory, Technical Operations, and Commercial.
* Ensure GxP employees complete required training.
* Represent QA in internal and external meetings.
WHAT YOU'LL BRING
Required
* Bachelor's degree in a life-science or related field.
* 10+ years of experience in biopharmaceutical or pharmaceutical Quality.
* Strong knowledge of domestic and international GMP regulations.
* Proven experience building and maintaining Quality Systems.
* Experience partnering with multi-disciplinary teams across Regulatory, Technical Operations, and Commercial.
* Strong organizational and communication skills, with the ability to resolve challenges independently.
Preferred
* Experience with electronic quality systems such as Veeva, TrackWise, or MasterControl.
* Experience supporting Quality System compliance for combination products.
* Experience operating in a global, multi-region regulatory environment (US, EU, UK, MENA, LATAM, APAC).
WHAT WE OFFER
* Competitive base salary, annual performance bonus, and equity — so you share in the value you help create
* Comprehensive health coverage: medical, dental, and vision
* 401(k) with company match
* Generous paid time off and company holidays
* A high-trust, low-bureaucracy culture with direct access to leadership and real room to grow
* Mission-driven work that helps preserve sight for patients who are counting on it
COMPENSATION
In keeping with our commitment to pay transparency, the good-faith base salary range for this role is $180,000-$220,000, with an annual target bonus of 20%. This role is also eligible for a meaningful equity grant, reflecting the opportunity to build lasting value at a company at a commercial inflection point. Final compensation reflects experience, skills, and location.
OUR COMMITMENT
Outlook Therapeutics is an equal opportunity employer. We are committed to building an inclusive environment where every team member can do their best work, and we consider all qualified applicants without regard to race, color, religion, sex, sexual orientation, gender identity, national origin, age, disability, veteran status, or any other characteristic protected by law. #J-18808-Ljbffr
Director, Quality Systems and GxP Compliance in arkansas at Unknown Company
This position is listed as full time and able to be worked remotely.