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Senior Manager, Manufacturing Operations

Job in Vacaville, Solano County, California, 95688, USA
Listing for: Yahoo! Inc.
Full Time position
Listed on 2026-08-22
Job specializations:
  • Manufacturing / Production
    Operations Management, Quality Engineering, Regulatory Compliance Specialist, Production QC/QA
Salary/Wage Range or Industry Benchmark: 140000 - 160000 USD Yearly USD 140000.00 160000.00 YEAR
Job Description & How to Apply Below

Senior Manager, Manufacturing Operations

About Oath:

Oath is a leading microbial sciences company that utilizes natural soil biology to offer innovative solutions to some of the most critical challenges facing our planet - the climate crisis and the shift to sustainable agriculture. We imagine a world where these crises are not just alleviated, but reversed, replenishing Earth's microbiomes.

Our solution has moved beyond the lab and into real-world deployment, focused on improving farmer livelihoods with teams in Rwanda, Europe, the United States, and expanding. When you join Oath, you become part of a collaborative network that prioritizes high quality scientific work. You will be working alongside trained scientists, talented commercial teams, and a broad network of partners—an ecosystem designed to help you do your best work and grow your capabilities.

Position Summary:

The Senior Manager, Manufacturing Operations will help build and operationalize the systems, processes, and standards required to scale Oath’s manufacturing activities. This role will work internally across production, quality, supply chain, regulatory, and technical teams and externally with vendors to ensure our processes are well documented, controlled, and ready for reliable execution across internal and external manufacturing partners.

Key Responsibilities:

  • Develop and maintain manufacturing SOPs, work instructions, specifications, and process documentation.
  • Establish and maintain product and raw material specifications and associated documentation.
  • Coordinate preparation and maintenance of SDSs, COAs, COCs, batch records, and release documentation.
  • Support QC and batch release processes, ensuring required testing and documentation are completed prior to release.
  • Drive manufacturing change control and process change management.
  • Coordinate activities across manufacturing, quality, regulatory, supply chain, shipping, and planning.
  • Support technology transfer and operational readiness with external manufacturing partners and CDMOs.
  • Establish, track, and report manufacturing KPIs, including yield, success rate, quality, throughput, and operational performance.
  • Identify operational gaps and implement systems and processes that improve manufacturing reliability and scalability.
  • Audit Oath vendors for compliance with process and procedures

Qualifications:

  • BS or MS in biotechnology, biochemical engineering, chemical engineering, microbiology, or a related discipline.
  • 7+ years of experience in biotechnology, biomanufacturing, fermentation, or a related manufacturing environment.
  • Strong experience with manufacturing documentation, SOPs, specifications, and controlled processes.
  • Experience working across manufacturing, quality, supply chain, and technical organizations.
  • Experience working with external manufacturers or CDMOs is a plus.
  • Familiarity with Google Suite, Excel, Slack and similar tools is a plus

Location: Hybrid, with regular presence at Oath’s Vacaville, California site. Ability to travel 20% of the time (Europe & Africa).

Job Type: Full-time, exempt position in the United States. At this time, Oath, Inc. is not able to provide visa sponsorship or work authorization support.

Compensation: $140,000 - $160,000/year + equity

  • Health insurance
  • Paid time off
  • Stock options
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Position Requirements
10+ Years work experience
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