San Carlos, California, United States · On-site
$210k–$280k/yr
Attovia Therapeutics, Inc., is seeking a Sr. Director/Director of Quality Assurance to lead our quality function and oversee the performance of our external CDMO/CRO partners, who execute the majority of our GMP manufact…
Skills: Quality Assurance, Vendor Quality Management, CDMO Oversight, CRO Oversight, GMP Compliance
San Carlos, California, United States · On-site
$235k–$280k/yr
Attovia Therapeutics, Inc., is seeking an SEC Controller to lead our external financial reporting function. Reporting directly to the CFO, this role is responsible for all SEC filings and technical accounting, ensuring o…
Skills: SEC Reporting, US GAAP, Technical Accounting, SOX Compliance, Tax Management
San Carlos, California, United States • On-site
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Lead the quality function by overseeing external CDMO and CRO partners to ensure compliant GMP manufacturing, testing, and clinical activities. Responsible for managing the internal Quality Management System, conducting vendor audits, and ensuring all outsourced activities meet global regulatory expectations.
Requires a Bachelor's or Master's degree in Life Sciences or a related field with over 12 years of QA experience in biotech/pharma, specifically managing outsourced GMP relationships. Must have deep knowledge of FDA, EMA, and ICH guidelines and experience with biologics or sterile injectables.
Attovia Therapeutics, Inc., is seeking a Sr. Director/Director of Quality Assurance to lead our quality function and oversee the performance of our external CDMO/CRO partners, who execute the majority of our GMP manufacturing, testing, and clinical activities. Reporting directly to the Quality Officer, this role is responsible for vendor quality management: qualifying and auditing CDMOs/CROs, negotiating and maintaining Quality Agreements, performing final quality review for batch release and lot disposition, and ensuring the company's internal Quality Management System (QMS) ties together all outsourced activity into a single, inspection-ready compliance picture. This role partners closely with CMC, Clinical Operations, Nonclinical/Preclinical Development, and Regulatory Affairs teams to ensure that our outsourced partners consistently deliver compliant, high-quality work that meets regulatory expectations and protects patient safety.
\nKey ResponsibilitiesQuality Strategy & Leadership
CDMO Quality Oversight
Clinical & Nonclinical CRO Oversight
Vendor Qualification, Audits & Quality Agreements
Quality Management System (QMS)
Attovia is a clinical-stage biopharmaceutical company developing next-generation biotherapeutics for immune-mediated diseases with high unmet need. All our product candidates have been internally discovered using our ATTOBODY biparatopic biologics platform. Our ATTOBODY platform uses an evolution-driven, high-throughput process which allows for rapid discovery and creation of a high diversity of potential product candidates.
Our culture is centered around five core pillars:
• Integrity
• Learning & Growth
• Drive for Excellence
• Innovation
• Teamwork & Collaboration
We take pride in fostering a strong team and dynamic work environment, and we are seeking individuals who align with our values and contribute to a positive and impactful workplace.
Attovia is located in San Carlos, CA.
Attovia is an equal opportunity employer. All applicants will be considered for employment without attention to race, color, religion, sex, sexual orientation, gender identity, national origin, veteran or disability status.
Learn more about Attovia: www.attovia.com
Creating medicines for immune-mediated disease using ATTOBODY®, a proprietary biologics platform for complex biologics.
Attovia is a clinical-stage biopharmaceutical company developing next-generation therapeutics for immune-mediated diseases with high unmet need. We leverage ATTOBODY™, our proprietary biologics platform, to generate first-in-class and best-in-class therapeutics. All of Attovia’s current product candidates have been internally discovered using our proprietary ATTOBODY biparatopic biotherapeutics platform. The ATTOBODY platform uses an evolution-driven, high-throughput process enabling rapid discovery and efficient generation of precision-designed complex biologics, including multispecifics, conditional bispecifics, and ATTOBODIES targeting multi-transmembrane proteins. Attovia’s most advanced product candidates target clinically validated pathways with significant commercial relevance where differentiated molecular design may address important limitations of current standards of care. Our discovery stage programs pursue novel targets and novel concepts in disease biology.
Offices: 1091 Industrial Rd, Suite 310, San Carlos, California 94070, US
Creating medicines for immune-mediated disease using ATTOBODY®, a proprietary biologics platform for complex biologics.
Attovia is a clinical-stage biopharmaceutical company developing next-generation therapeutics for immune-mediated diseases with high unmet need. We leverage ATTOBODY™, our proprietary biologics platform, to generate first-in-class and best-in-class therapeutics. All of Attovia’s current product candidates have been internally discovered using our proprietary ATTOBODY biparatopic biotherapeutics platform. The ATTOBODY platform uses an evolution-driven, high-throughput process enabling rapid discovery and efficient generation of precision-designed complex biologics, including multispecifics, conditional bispecifics, and ATTOBODIES targeting multi-transmembrane proteins. Attovia’s most advanced product candidates target clinically validated pathways with significant commercial relevance where differentiated molecular design may address important limitations of current standards of care. Our discovery stage programs pursue novel targets and novel concepts in disease biology.
Offices: 1091 Industrial Rd, Suite 310, San Carlos, California 94070, US
