Manager/Sr. Manager, Quality Assurance
Manager/Sr. Manager, Quality Assurance
BridgeBio
United States
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QED Therapeutics, an affiliate of BridgeBio Pharma, focuses on developing targeted treatments for FGFR-driven skeletal dysplasias, particularly Achondroplasia. Achondroplasia is the most common form of genetically-driven short stature, which causes potentially debilitating medical complications. With our experimental therapeutic candidate, infigratinib, we seek to provide an option to children living with Achondroplasia and their families.
Our Business Is Inspired By Our Values
- PUT PATIENTS FIRST
- LET SCIENCE SPEAK
- EVERY MINUTE COUNTS
- THINK INDEPENDENTLY
- BE RADICALLY TRANSPARENT
BridgeBio is a biopharmaceutical company founded to discover, create, test, and deliver transformative medicines to treat patients who suffer from genetic diseases and cancers with clear genetic drivers. We bridge the gap between remarkable advancements in genetic science in academic institutions and the delivery of meaningful medicines to patients. Founded in 2015, the company has built a portfolio of 30+ drug development programs ranging from preclinical to late-stage development in multiple therapeutic areas including genetic dermatology, precision oncology, cardiology, endocrinology, neurology, pulmonology, and renal disease, with two approved drugs.
Our focus on scientific excellence and rapid execution aims to translate today’s discoveries into tomorrow’s medicines. We have U.S. offices in San Francisco, Palo Alto, Raleigh, and with small satellites in other parts of the country. We also have international offices in Montreal, Canada, and Zug, Switzerland, and are expanding across Europe.
To learn more about our story and company culture, visit us at https://www.qedtx.com/ | https://bridgebio.com
Who You Are
Reporting to the Associate Director, Quality Assurance, the Manager/Sr. Manager, Quality Assurance will assist in the quality oversight and management of GxP activities internally at QED and externally with QED vendors, consultants and service providers including, but not limited to, quality systems management and external document review and approval. The ideal candidate will have quality assurance experience working in the biotech/pharmaceutical sector.
Responsibilities
- Provide QA support for analytical development and commercialization
- Assist in the development, implementation and maintenance of analytical trending including stability
- Monitor ongoing compendial updates and communicate to cross functional teams
- Provide guidance, review and approve external laboratory investigations
- Assist in inspection readiness activities at QED
- Author and implement QA GXP standard operating procedures (SOPs)
- Supports the management, maintenance, and evaluation of QED’s Quality Management Systems and processes for optimization and continuous improvement
- Perform internal and external document review and approval
No matter your role at BridgeBio, successful team members are:
- Patient Champions, who put patients first and uphold strict ethical standards
- Entrepreneurial Operators, who drive toward practical solutions and have an ownership mindset
- Truth Seekers, who are detailed, rational, and humble problem solvers
- Individuals Who Inspire Excellence in themselves and those around them
- High-quality executors, who execute against goals and milestones with quality, precision, and speed
- Bachelor's degree in a chemistry, another scientific discipline or equivalent experience
- Minimum of 5 years pharmaceutical industry experience in Quality Assurance, or other relevant roles
- Experience with analytical instrumentation, methods, validation, and investigations, including stability program management
- Knowledge of applicable GXP regulations (e.g., CFRs and ICH)
- Ability to build relationships and work collaboratively with a variety of individuals within the department, company, and external vendors
- Ability to simultaneously handle multiple project issues while dealing with time demands, incomplete information, or unexpected events
- Patient Days, where we are fortunate to hear directly from individuals living with the conditions we are seeking to impact throughout the year and learn how we can improve our efforts
- A culture inspired by our values: put patients first, think independently, be radically transparent, every minute counts, and let the science speak
- An unyielding commitment to always putting patients first. Learn more about how we do this here
- A de-centralized model that enables our program teams to focus on advancing science and helping patients. Our affiliate structure is designed to eliminate bureaucracy and put decision-making power in the hands of those closest to the science
- A place where you own the vision – both for your program and your own career path
- A collaborative, fast-paced, data-driven environment where we inspire ourselves and each other to always perform at the top of our game
- Access to learning and development resources to help you get in the best professional shape of your life
- Robust and market-competitive compensation & benefits package (Base, Performance Bonus, Equity, health, welfare & retirement programs)
- Flexible PTO
- Rapid career advancement for strong performers
- Potential ability to work on multiple BridgeBio Pharma programs across multiple therapeutic areas over time
- Partnerships with leading institutions
- Commitment to Diversity, Equity & Inclusion
Salary
$125,000—$175,000 USD
-
Seniority level
Mid-Senior level -
Employment type
Full-time -
Job function
Quality Assurance -
Industries
Biotechnology Research
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