BridgeBio Pharma

Compensation

Full 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. Affiliate Overview Calcilytix Therapeutics, an affiliate within BridgeBio Pharma, is developing encaleret, a negative allosteric modulator of the calcium-sensing receptor (CaSR) for the treatment of Autosomal Dominant Hypocalcemia Type 1 (ADH1), a genetic cause of hypoparathyroidism. Encaleret is currently being evaluated in a Phase 3 clinical study and has received Orphan Drug Designation from the US FDA, EMA, and PMDA as well as Fast Track Designation from the US FDA. Results from the Phase 2b clinical study of encaleret in patients in ADH1 were published in the New England Journal of Medicine. What You'll Do The Quality Control Manager at Bridge Bio will be an important part of our Quality Control group supporting BridgeBio subsidiaries (Calcilytix and MLBio and Eidos.) The Quality Control Manager is responsible for ensuring that all activities conducted at the analytical Contract Manufacturing Organizations (CMO) laboratories are conducted in compliance with Current Good Manufacturing Practices (cGMP). A large portion of the position’s responsibilities will be the critical review of analytical test packages for release testing, in-process testing, and stability testing of clinical/commercial supplies (both DS and DP). This will involve verification that test methods/procedures are followed as written, and documentation is both complete and accurate. The position will ensure that the data is reviewed in a timely manner. The position requires close collaboration with both Quality Assurance (QA) and the analytical contract laboratories. A working knowledge of various analytical techniques including HPLC, GC, GC/MS, LC/MS, ICP, dissolution, UV, NMR, XRPD, Karl Fischer titration, DSC, TGA, and wet chemistry is required. A thorough and sophisticated understanding of relevant ICH guidelines and health authority expectations is expected. Additional responsibilities include review of analytical data with respect to late development/launch preparation activities including (but not limited to): analytical method transfer, phase appropriate method validation for both drug substance and drug product methods, and review of data for analytical sections of regulatory submissions (both DS and DP). Excellent communication skills (both verbal and written) a must. Responsibilities Review of analytical data for release, stability, and in-process testing at the contract manufacturing organizations in a timely manner Oversight of laboratories including investigations for out of specification, out of trend, deviations, and/or anomalous results Follow up with the contract laboratories to correct any deficiencies/omissions in the provided test packages Submitting test packages to QA for their review and loading all data into the electronic storage program Review of analytical data related to reference standard qualification, method validation and method transfer activities Travel, when necessary, to analytical testing sites or other sites Able to communicate results both internally and externally through oral and written updates and formal reports as necessary Create or review BBio Standard Operating Procedures as it pertains to Quality Control or management of contract analytical laboratories Where You'll Work This is a US-based remote role that will require quarterly, or as needed, visits to our San Francisco office. Occasional travel to CMO laboratories may also be required. Who You Are M.S./B.S. in life sciences, ideally Chemistry, Analytical Chemistry preferred 5+ years’ experience in Quality Control in a pharmaceutical setting with solid knowledge of Good Manufacturing Practices (cGMP) 2+ years management experience Ability to communicate effectively with vendors regarding project scope, scientific results, and project updates Proven abilities in leadership and personnel management Strong oral and written communication skills Excellent organizational and planning skills and high attention to detail Demonstrated strong analytical skills, and the ability to work independently against multiple deadlines Sophisticated understanding how and when to appropriately apply the cGMP requirements; ability to distinguish regulated and non-regulated activities 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 $120,000—$150,000 USD