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Quality Assurance Specialist

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Are you ready to join Connecticut Innovation’s vibrant community of innovators? Connecticut Innovations (“CI”) is Connecticut’s strategic venture capital arm, and we are passionate about serving our portfolio of 220+ companies across various industries, with strengths in life sciences, technology, and climate tech.


Come join First-in-Class Dermatology Drugs | Veradermics!


Veradermics Corporate Overview


Veradermics is a late clinical-stage aesthetics and dermatology focused biopharmaceutical company developing first-in-class therapeutics for common dermatologic conditions. Backed by an oversubscribed $150 million Series C financing led by top-tier global investors, we are entering an exciting new chapter. This funding propels the development of our lead candidate, VDPHL01, a nonhormonal oral therapeutic for androgenetic alopecia (AGA) and patterned hair loss (PHL). We are currently enrolling Phase 3 trials as we work to deliver transformative solutions and redefine the standard of care in dermatology


In addition to VDPHL01, our pipeline includes assets addressing widespread, high-unmet-need conditions such as common warts and molluscum contagiosum. At Veradermics, we combine scientific rigor with a vision for impactful innovation that makes a lasting difference in patients lives.


Why Work at Veradermics


  • You Can Be Part of a Meaningful Mission - Veradermics aims to create a paradigm shift in medical dermatology by bringing pharmaceutical innovation to the treatment of common skin conditions that currently lack meaningful therapeutic advances and have been neglected by traditional pharma.
  • Veradermics Has Significant Growth Potential Veradermics Product Candidates Have Cumulative Revenue Estimates of > $6B/Year.
  • We have been featured in Forbes, Slate, The New York Post, The Hartford Courant, The Kansas City Star, and many other multi-media platforms.


Quality Assurance/Regulatory Specialist | Position Overview


The Quality Assurance/Regulatory Specialist reports to the VP of Quality. This role will oversee QMS document control as the Administrator of the eQMS and LMS system to ensure documentation complies with internal polices and external regulations (FDA, ICH). This role requires a strong ability to collaborate with various teams, document procedures, and stay current with changing industry standards.


  • Effectively communicates within the organization
  • Create, revise and maintain controlled documentation
  • Consults with management to develop and implement solutions for achieving quality related objectives
  • Support Change Controls and Corrective and Preventive Actions (CAPA)
  • A strong focus on technical writing
  • Maintain Quality initiative key performance indicators (KPIs)
  • Perform quality control review of Trial Master File (TMF) transfers to ensure accuracy and compliance with regulatory and sponsor requirements
  • Perform other related duties as assigned or necessary; remain flexible and adaptable in work schedules and assignments as defined by departmental and organizational needs


Candidate Profile | Who You Are


  • A bachelor’s degree, or a 4-year equivalent degree, 2-10 years of total quality assurance experience will be considered
  • Highly organized with excellent communication skills and the ability to work both independently and as part of a team
  • Excellent communication skills (oral and written)
  • Excellent planning and time management skills
  • Proficient in Microsoft Office Suite, experience with eQMS and LMS systems is a plus.
  • Knowledge of clinical operations, GCP, and regulatory compliance is a plus.
  • Resourceful and proactive when issues arise.
  • Thrive in a fast-paced environment with constantly changing and competing priorities.
  • Highly transparent, ethical, and driven.
  • Relentless attention to detail and the ability to be a creative self-starter and team player.
  • Willingness to work a flexible schedule if necessary.


Company Culture


Veradermics is a small and tight-knit operation where our team works tirelessly to develop innovative new therapeutics for dermatology. We hold ourselves to an incredibly high standard and are looking for an exceptional person who is ready to be an integral team member and make a positive impact on the practice of medicine. We strongly appreciate positivity, curiosity, and, above all else, the ability to stay organized and get things done at the highest level and on time. We are incredibly conscious of creating a comfortable, flexible environment that cultivates the desire to be engaged, ask questions, and feel a vested interest in our team's success. Most importantly, you should value honest and direct communication as you recognize that this is the best way for any individual or team to continuously learn and grow. Accomplishing our collective goals will be fun but also complex.


What It's Like To Work With Us


We’re passionate about dermatology and about improving the lives of individuals suffering from common skin conditions. The therapeutics you help us develop will impact the quality of life of millions of people suffering from conditions ranging from common warts to alopecia areata. We strive to do our personal best and to encourage others to do their best. We also believe in treating others with respect and want to create a company that people are excited to work for.


Location and Hybrid Schedule


  • Location: New Haven, CT at District New Haven (470 James Street)
  • Hybrid Schedule : 1 to 2 days onsite


Equal Opportunity Employer


Veradermics is an equal opportunity employer. All employment decisions are based on qualifications, merit, and business needs, without regard to race, color, religion, gender, gender identity or expression, sexual orientation, national origin, disability, or age.

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