About Apogee Therapeutics
Founded in 2022, Apogee Therapeutics, Inc. (Ticker: APGE) is a well-funded, Nasdaq listed company that offers the opportunity to work in a fast-paced, highly dynamic environment. At Apogee, you can actively contribute to shaping the company culture, take on various roles and responsibilities, and grow professionally.
Apogee Therapeutics, Inc. is a biotechnology company seeking to develop differentiated biologics for the treatment of atopic dermatitis, chronic obstructive pulmonary disease and other inflammatory and immunology indications with high unmet need. Our antibody programs are designed to potentially overcome limitations of existing therapies by targeting well-established mechanisms of action and incorporating advanced antibody engineering to optimize half-life and other properties. We seek to reshape the current standard of care for inflammatory and immune diseases because we believe people living with these diseases deserve the best possible treatment, and we refuse to stop at “good enough.”
We are a fast-paced company committed to building an exceptional company culture, founded on our C.O.R.E. values: Caring, Original, Resilient and Egoless.
If this sounds like you, keep reading!
Role Summary
We are seeking a dynamic and results-driven Associate Director of Clinical Quality Assurance (QA) to join our team. This key role will be responsible for assisting with establishing and supporting a robust QA system for our clinical operations, ensuring compliance with regulatory standards, and promoting a culture of quality throughout the organization.
Key Responsibilities
- Assist QA Leadership with development and execution of planned QA audit schedules supporting clinical study programs.
- Independently performs assigned GCP audits e.g. clinical investigator sites, vendor qualifications, trial master files, internal processes and clinical study documents.
- Partner effectively with clinical functions and provide quality guidance to drive quality in clinical data and documentation generated.
- Facilitate investigation of reported quality events, evaluate and approve appropriateness of CAPAs proposed to mitigate risk of issue re-occurrence.
- Contribute to the development and maintenance of clinical QA procedures and other governance standards as needed.
- Assist in the periodic reporting of key quality metrics to leadership to assist in driving improvements in GCP compliance across the organization.
- Assist in the development and/or delivery of GCP training topics and quality standards as directed.
- Assist QA Leadership in fostering a culture of quality and continuous improvement within the organization, emphasizing the importance of compliance, data integrity, and patient safety in support of corporate goals.
- Collaborate with Process Excellence team in support of inspection readiness activities.
- Perform key activities during regulatory authority inspection and/or external audits as directed by QA Leadership.
The Ideal Candidate will Possess
- Bachelor's degree in a relevant biological sciences or equivalent is required.
- Advanced degree a plus.
- Minimum of 7 years of direct audit experience in GCP quality assurance within the biotech or pharmaceutical industry, with increasing responsibilities in the Clinical QA function.
- In-depth working knowledge of GCP regulations and guidelines, including FDA, EMA, and ICH requirements.
- Extensive experience using electronic QMS to monitor, report, and track quality tasks and key quality performance indicators.
- Strong communication (oral and written), effective interpersonal skills with the ability to listen and drive change.
- Excellent problem-solving and critical thinking abilities.
- Flexible and creative to meet the needs and challenges of a growing, dynamic company.
- Focus on fostering a culture of collaboration and teamwork.
- Ability to manage multiple projects with aggressive timelines and changing priorities.
- Ability and willingness to travel up to 20% per year including all company meetings.
The anticipated salary range for candidates for this role will be $170,000-$190,000/ year. The final salary offered will depend on several factors, which may include, but is not limited to relevant years of experience, educational background, and geography.
What We Offer
- A great culture, grounded in our C.O.R.E. values: Caring, Original, Resilient and Egoless
- Opportunity to work in a fast-paced, highly dynamic environment where you help shape the culture and company, wear multiple hats, and learn quickly
- Market competitive compensation and benefits package, including base salary, performance bonus, equity grant opportunities, health, welfare & retirement benefits
- Flexible PTO
- Two, one-week company-wide shutdowns each year
- Commitment to growing you professionally and providing access to resources to further your development
- Apogee offers regular all team, in-person meetings to build relationships and problem solve
E-Verify Participation: As part of the I9 verification of authorization to work in the US, Apogee participates in E-Verify. To learn more about E-Verify please review this poster.
Apogee Therapeutics is proud to be an Equal Opportunity employer. All qualified applicants will receive consideration for employment without regard to sex, gender identity, sexual orientation, race, color, religion, national origin, disability, protected Veteran status, age, or any other characteristic protected by law.
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