Site Production Flow Manager

Posted 9 Days Ago
Be an Early Applicant
2 Locations
In-Office
Mid level
Biotech • Pharmaceutical
The Role
The Site Production Flow Manager oversees batch release flow, coordinates across departments, manages risks, and optimizes KPIs for timely production.
Summary Generated by Built In

At Bavarian Nordic, we are committed to saving and improving lives by unlocking the power of the immune system. Our commercial product portfolio includes market-leading vaccines against smallpox, mpox, rabies, tick-borne encephalitis, typhoid fever, and cholera. We excel in R&D innovation, manufacturing, and commercialization, striving to improve people's health and quality of life worldwide, protecting our tomorrow.

Bavarian Nordic is progressing through a data maturity journey spanning ERP foundation, data governance, and advanced digital capabilities across Supply Chain, Global Operations and beyond.

To ensure we act with foresight, diligence, and timely execution, we are looking to hire a Site Production Flow Manager for our biggest manufacturing site – in Kvistgaard (hybrid role between Kvistgaard/Hellerup). You will report to the local Supply Chain Lead and become part of a team of five.

The role
As Site Production Flow Manager, you will have end-to-end visibility and coordination of batch flow and release status across the site. Your main focus is to ensure that all planning and prioritization decisions are based on accurate, real-time release data and that batch flow from production through QA/QC to release is transparent, predictable, and aligned with supply priorities. This role is the execution truth engine of Site Supply Chain.

Key Responsibilities
 

  • Own end-to-end oversight of batch release flow, ensuring accurate, real-time visibility of status, timelines, and downstream impacts

  • Coordinate across QA, QC, Manufacturing, and Supply Chain to drive timely batch progression and resolve bottlenecks

  • Proactively manage release risks, including identifying delays, escalating issues with clear impact, and driving mitigation actions

  • Deliver structured release updates and risk inputs to S&OE, ensuring data accuracy, completeness, and readiness for decision-making

  • Own and optimize release KPIs (e.g., cycle time, delays), including developing dashboards and driving data-based performance tracking

  • Act as business owner of batch tracking tools (e.g., BFM), ensuring data quality, adoption, and alignment with actual batch flow and inventory risk

What you bring

To become a success in this role, you bring 3–6 years of experience from pharma/biotech operations within QA, QC, Manufacturing, or Supply Chain, and a solid understanding of batch release in a GMP environment. You are structured, detail-oriented, and strong at driving cross-functional coordination and follow-up. With a data-driven mindset, you create transparency, identify risks early, and ensure alignment across QA, Manufacturing, and Supply Chain—while constructively challenging when needed.

Success in the first 6 months will include

  • Clear visibility and control of batch flow, with reliable and predictable release timelines

  • Strong cross-functional alignment, reducing release-related delays and surprises

  • Established KPI reporting that supports proactive decision-making

Full proficiency in Danish and English is required.

Why this role
This is a highly impactful role at the heart of site operations, ensuring that batch release flows smoothly, predictably, and with full transparency. You will play a key role in connecting QA, Manufacturing, and Supply Chain, driving alignment and enabling better, data-driven decision-making across the site. With direct influence on timelines, risk mitigation, and operational performance, this role offers the opportunity to create real impact by reducing complexity, increasing predictability, and strengthening how we manage release and supply.

Application
If you are ready to take on a pivotal role in a growing organization and drive meaningful change in healthcare, apply now and join Bavarian Nordic in our mission to improve health outcomes and foster sustainable growth.

Please note that for this position, we do not support any relocation package.

We kindly request that headhunters or recruitment agencies refrain from contacting us regarding this position.

Bavarian Nordic is a global vaccine company with a mission to improve health and save lives through innovative vaccines. We are a preferred supplier of mpox and smallpox vaccines to governments to enhance public health preparedness and have a leading portfolio of travel vaccines. We are headquartered in Denmark and have manufacturing, research, and sales offices across Europe and North America.

Bavarian Nordic is an Equal Opportunity Employer. All qualified applications will receive consideration for employment and will not be discriminated against based on race, color, sex, sexual orientation, gender identity, national origin, disability, or protected veteran status.

For more information, visit www.bavarian-nordic.com

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Skills Required

  • 3-6 years of experience from pharma/biotech operations
  • Solid understanding of batch release in a GMP environment
  • Full proficiency in Danish and English
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The Company
1,692 Employees
Year Founded: 1994

What We Do

Bavarian Nordic is a global biotechnology company focused on the development, manufacturing, and commercialization of innovative vaccines, with a mission to improve health and save lives.

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