Job description
Mavericks Wanted
When was the last time you achieved the impossible? If that thought feels overwhelming, you might want to pause here, but if it sparks excitement…read on
In 2015, we pioneered a “moneyball for biotech” approach, pooling projects and promising early-stage research from academia together under one financial umbrella to reduce risk and unleash innovation. This model allows science and small teams of experts to lead the way. We build bridges to groundbreaking advancements in rare disease, and develop life-changing medicines for patients with unmet needs as fast as humanly possible.
Together we define white space, push boundaries and empower people to solve problems. If you’re someone who defies convention, join us and work alongside some of the most respected minds in the industry. Together, we’ll ask “why not?” and help reengineer the future of biopharma.
What You’ll Do
Reporting to the Senior Vice President of Quality Assurance, the Executive Director, Quality Operations is a vital member of the BridgeBio Quality leadership team, responsible for driving and delivering the activities necessary to develop, implement, and continuously improve BridgeBio’s GXP Quality Management System (QMS). The Executive Director will be responsible for the implementation and improvement of electronic systems in support of QMS processes, plan for and support future clinical and commercial manufacturing and supply chain needs, and support or lead quality initiatives to support the growth of the organization.
Responsibilities
- Select, implement, manage, and oversee GxP electronic systems
- Manage a portfolio of interrelated continuous improvement projects and initiatives
- Develop, implement, manage, continuously improve, and oversee: Document Management, Training Management, Change Control, Management Review (MR), Annual Product Quality Review (APQR), Deviation/CAPA/ Risk Management, and GxP Computer System Assurance
- Guide and support GxP process owners with implementation and improvement /optimization of key functional area processes
- Establish and improve policies, standards and standard operating procedures for efficient and compliant management of GxP QMS processes
- Establish, track and report quality metrics for QMS processes and present improvement opportunities at Management Review meetings
- Implement phase appropriate, risk-based, fit-for-purpose approaches to QMS processes
- Support the BridgeBio Quality management team in ensuring that QMS processes comply with applicable regulatory standards, regulations and guidelines
- Maintain awareness of new regulations, technologies, trends and apply as relevant
- Manage resources to achieve company, department and functional area goals and objectives
- Contribute to the development and maintenance of a positive team-focused company culture
- Day to day support, development, and management of direct reports
Where You’ll Work
This is a U.S.-based remote role that will require quarterly, or as needed, visits to our San Francisco Office.
Who You Are
- BA or BS degree in a scientific discipline or comparable experience
- 15+ years of experience in a pharmaceutical or biotech environment in Quality Assurance, Quality Control, QMS or a GxP operational role
- Minimum of 5 years of managing Quality Management Systems
- Minimum of 5 years of experience with Phase 3 and/or commercial bio-pharm manufacturing
- 3+ years of experience in an outsourced manufacturing environment
- Strong technical skillset and experience in implementing and validating cloud-based (hosted) computer systems
- Position requires 10-20% travel
- Thorough knowledge of applicable regulations such as 21CFR Part 11, 210, and 211; ICH Q1–Q11 and E1-E8
Rewarding Those Who Make the Mission Possible
We have high expectations for our team members. We make sure those working hard for patients are rewarded and cared for in return.
Financial Benefits:
- Market leading compensation
- 401K with 100% employer match on first 3% & 50% on the next 2%
- Employee stock purchase program
- Pre-tax commuter benefits
- Referral program with $2,500 award for hired referrals
Health & Wellbeing:
- Comprehensive health care with 100% premiums covered - no cost to you and dependents
- Mental health support via Spring Health (6 therapy sessions & 6 coaching sessions)
- Hybrid work model - employees have the autonomy in where and how they do their work
- Unlimited flexible paid time off - take the time that you need
- Paid parental leave - 4 months for birthing parents & 2 months for non-birthing parents
- Flex spending accounts & company-provided group term life & disability
- Subsidized lunch via Forkable on days worked from our office
Skill Development & Career Paths:
- People are part of our growth and success story - from discovery to active drug trials and FDA pipelines, there are endless opportunities for skill development and internal mobility
- We provide career pathing through regular feedback, continuous education and professional development programs via LinkedIn Learning, LifeLabs, Spring Health & BetterUp Coaching
- We celebrate strong performance with financial rewards, peer-to-peer recognition, and growth opportunities
At BridgeBio, we strive to provide a market-competitive total rewards package, including base pay, an annual performance bonus, company equity, and generous health benefits. Below is the anticipated salary range for candidates for this role who will work in California. The final salary offered to a successful candidate will depend on several factors that may include but are not limited to the type and length of experience within the job, type, and length of experience within the industry, educational background, location of residence and performance during the interview process. BridgeBio is a multi-state employer, and this salary range may not reflect positions based in other states.
Salary
$260,000—$300,000 USD
