BridgeBio Pharma, Inc.

QA Operations - Drug Product, QA Manager

BridgeBio Pharma, Inc.$150K — $175K *
Pharmaceuticals & Biotech
8 - 10 years of experience
Job Overview by Ladders

Qualifications

  • Bachelor's Degree in a science discipline with 8+ years of experience in biopharmaceutical or contract research organization
  • Strong knowledge of GMP, SOPs, Quality Systems, ICH and GxP principles
  • Familiarity with FDA and clinical trial regulations
  • Experience in QC, Analytical Development, and process validation is highly desired
  • Excellent communication skills with a strong customer focus
  • Strong organizational skills with attention to detail
  • Willingness to travel up to 10% of the time

Responsibilities

  • Manage quality oversight at CMOs and act as QA operations lead
  • Review and manage manufacturing batch records and release activities
  • Author and perform quality review of SOPs and quality events
  • Lead drug product disposition processes
  • Communicate and escalate non-conformance issues to management
  • Support regulatory filing reviews and CMO audits
  • Participate in monitoring CMO performance on internal and external project teams

Benefits

  • Market-leading compensation
  • 401(k) with employer match
  • Employee Stock Purchase Program (ESPP)
  • 100% employer-paid medical, dental, and vision premiums for employees and dependents
  • Flexible paid time off and company-paid holidays
  • Comprehensive paid medical and parental leave benefits
  • Career development programs and continuous professional education opportunities
Full Job Description
What You'll Do

Manage quality oversight at Drug Product Contract Manufacturing Organizations (CMOs). Act as QA operations lead with assigned CMOs, including review of manufacturing batch records and batch release certificates. Ensure CMO SOPs and Master Batch Records are in compliance with cGMPs and serve as technical review for deviations, change records, protocols, and CAPAs generated from or pertaining to Calcilytix or other BridgeBio affiliates, as needed.

Responsibilities
  • Represent QA Operations on internal and external project teams, audits and inspections, and participate in monitoring of CMO performance
  • Review and manage master and executed manufacturing batch records from CMOs, including release activities, and related documents such as specifications, analytical and microbiological methods, stability study/protocols, process and method validation protocols and reports
  • Author and perform quality review of SOPs and quality events (deviations/investigations, OOSs/OOTs, change controls, supplier notifications, etc.)
  • Lead Disposition of Drug Product
  • Communicate/escalate manufacturing deficiencies/non-conformances to management, present issues during escalation, and work with CMOs to ensure timely resolution
  • Support review of regulatory filings
  • Support audit of CMOs


Where You'll Work

This role requires in-office collaboration 2-3x per week in our San Francisco office.

Who You Are
  • Bachelor's Degree in a science discipline with 8+ years of experience within a biopharmaceutical company, or contract research organization
  • Strong knowledge of GMP, SOPs, Quality Systems (e.g. Lot Release, Deviation, Change Control, CAPA,) ICH and GxP principles
  • Strong knowledge of FDA and other clinical trial regulations
  • Prior experience in QC, Analytical Development and process validation highly desired
  • Excellent verbal and written communication skills, with strong customer focus
  • Excellent organizational skills, ability to manage multiple tasks and competing priorities, and maintain meticulous attention to detail
  • Travel up to 10% total time


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

$150,000-$175,000 USD

As a global company, our comprehensive benefits may vary based on location. We have high expectations for our team members. We make sure those working hard for patients are rewarded and cared for in return.

For Full-Time U.S Based Roles:

Financial & Rewards
  • Market-leading compensation
  • 401(k) with employer match
  • Employee Stock Purchase Program (ESPP)
  • Pre-tax commuter benefits (transit and parking)
  • Referral bonus for hired candidates
  • Subsidized lunch and parking on in-office days

Health & Well-Being
  • 100% employer-paid medical, dental, and vision premiums for you and your dependents
  • Health Savings Account (HSA) with annual employer contributions, plus Flexible Spending Accounts (FSA)
  • Fertility & family-forming benefits
  • Expanded mental health support (therapy and coaching resources)
  • Hybrid work model with flexibility
  • Flexible, "take-what-you-need" paid time off and company-paid holidays
  • Comprehensive paid medical and parental leave to care for yourself and your family

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, & BetterUp Coaching
  • We celebrate strong performance with financial rewards, peer-to-peer recognition, and growth opportunities

About BridgeBio Pharma, Inc.

BridgeBio Pharma, Inc. is a biotechnology company that focuses on developing medicines for genetic diseases. The company's pipeline includes over 20 development programs, including treatments for diseases such as achondroplasia, adrenoleukodystrophy, and cystinosis. BridgeBio Pharma, Inc. also has a subsidiary, Eidos Therapeutics, which focuses on developing treatments for transthyretin amyloidosis. The company was founded in 2015 and is headquartered in Palo Alto, California.
Learn more about BridgeBio Pharma, Inc.
Size
576 employees
Market Cap
$1 billion
Industry
Net Income
-$448.7 million
Founded
2014
Revenue
$8.2 million
NASDAQ

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