Vera Therapeutics, Inc.

Associate Director, Drug Substance Manufacturing – Upstream Process

Vera Therapeutics, Inc. · Brisbane, CA

Posted about 3 months ago

or apply directly on Vera Therapeutics, Inc.'s site. We never take the application ourselves.

Is this posting real?

This role has been open
77 days
Vera Therapeutics, Inc.'s roles stay open a median of 71 days
Reposted
No
Salary listed
No
0% of Vera Therapeutics, Inc.'s roles list one
Ghost-job risk at Vera Therapeutics, Inc.
high
10 stale, 0 reposted of 11 open
Hiring momentum
20 roles opened in the last 90 days
↑ up vs. the prior 90 days
Last confirmed on the employer's board
2026-10-22

Measured from postings appearing on and disappearing from Vera Therapeutics, Inc.'s own greenhouse board since 2026-08-03. Full hiring picture for Vera Therapeutics, Inc..

About this role

The Associate Director, Drug Substance Manufacturing – Upstream Process at Vera Therapeutics will oversee all aspects of upstream biologics manufacturing, focusing on technology transfer, lifecycle management, and regulatory submissions. This role requires leading technical investigations, managing CMO relationships, and ensuring compliance with regulatory standards while collaborating with cross-functional teams.

Our read on this posting2.6out of 5
benefits
4/5
freshness
1/5
career value
4/5
role clarity
4/5
pay transparency
0/5

Scored from the posting itself — how clearly the role is described, how much it says about pay and benefits, and how recently it was listed. Not a judgement of Vera Therapeutics, Inc. as an employer.

What you need

  • MS in relevant life sciences or engineering discipline with a minimum of 5 years of Pharmaceutical/Biotechnology industry experience (or BS with 8 years of experience) in biologics drug substance upstream processes, technology transfer, and cGMP manufacturing operations
  • Extensive hands-on experience in upstream processing including cell bank management, cell culture (expansion and production), and harvest
  • Working knowledge of technology transfer, process validation, and routine management of GMP manufacturing
  • Experience in managing US/international CDMOs to help support commercial manufacturing of biologic drugs
  • Proven leadership and cross-functional management of CMC-related programs
  • Strong organizational and project management skills, including proficient use of MS Project and other tools

Nice to have

  • Experience in process development and/or manufacturing sciences and technology (MSAT) is preferred

What you get

  • Annual performance incentive bonus
  • New hire equity
  • Ongoing performance-based equity
  • Medical, dental, and vision insurance
  • 401k match
  • Flexible time off

Worth weighing

  • No specific mention of the technology stack or tools used in upstream processes
  • Role involves significant regulatory and compliance responsibilities which may be stressful
  • Remote position may require strong self-management and communication skills

Summarised from Vera Therapeutics, Inc.'s posting. Read the full original.

Listed by Vera Therapeutics, Inc. on their greenhouse job board, last confirmed open on 2026-10-22. PitchMeAI is not the employer.

More roles at Vera Therapeutics, Inc.

All 11 open roles at Vera Therapeutics, Inc. →

Apply to an Associate Director, Drug Substance Manufacturing – Upstream Process position at Vera Therapeutics, Inc. - Jobs near me at Brisbane, CA