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Open nowPosted 11 days ago

Senior Downstream Scientist, Manufacturing Product Support

AGC Biologics26 open roles

Where
Denmark
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Your applicationOpen nowSenior Downstream Scientist, Manufacturing Product SupportAGC Biologics · Denmark

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The clock on this job

Early applications get read.

12.3% of postings close within 7 days. Measured by our own scanner across the market. AGC Biologics postings stay open a median of 24 days.

Share of postings closed within
  1. 2.1%1 day
  2. 4.5%3 days
  3. 12.3%7 days
  4. 19.3%14 days
  5. 35.6%30 days
  6. 58.1%60 days
This job: posted 11 days ago

AGC Biologics median: 24 days open

The posting

Be part of a team supporting commercial manufacturing at AGC Biologics!

As a CDMO, AGC Biologics manufactures drugs for a variety of customers, supporting products from development through clinical and commercial production.

Now, you have the opportunity to join our Manufacturing Product Support department as a Downstream Scientist in one of our commercial teams. If you enjoy working in a team with great energy, strong collaboration, and room for having fun, this could be a great match for you!

In this role, you will bring your technical problem-solving skills, process understanding, and cGMP experience into a team with in-depth knowledge of product-specific requirements and close collaboration across departments. You will contribute to batch documentation, review, and deviation handling, supporting error-free and timely production execution while continuing to develop your skills.

The Role: Grow your downstream skills in Manufacturing Product Support

As a Senior Downstream Scientist, you will play an important role in supporting production and ensuring that manufacturing activities are executed efficiently and in compliance with quality requirements.

**Your Key Responsibilities Will Include

**

  • Creating and reviewing Master Production Records and supporting batch documentation.
  • Facilitating solutions when issues or breakdowns occur during batch execution.
  • Ensuring timely deviation closure, including systematic problem-solving and root cause investigations, as well as handling other quality documentation.
  • Over time, taking on additional responsibilities such as representing the team in customer meetings, supporting audits and inspections, capturing learnings, and implementing continuous process improvements.

Our team works closely together to support production, combining technical expertise with a positive and collaborative working environment.

_"What makes our team a fantastic and unique place to be is our teamwork. We are sharing such a good spirit and high energy - and having fun!"

_Nezrab Sedighi, Manager of Manufacturing Product Support

As part of the role, you will also participate in our duty phone arrangement, providing on-call and shopfloor scientist support during critical process steps. You can expect to be on call for approximately 24 hours, three times a month.

What You Bring: Experience with GMP and downstream processes

We are looking for a Senior Downstream Scientist with a strong scientific background and hands-on experience from a cGMP manufacturing environment.

A BSc or MSc in natural or life sciences is preferred, along with at least four years of experience working in a manufacturing team operating under cGMP, preferably within the pharmaceutical industry.

Experience from commercial GMP manufacturing is an advantage, but not a requirement. We particularly value experience from a similar production support role involving downstream processes.

You bring experience in writing, reviewing, and approving GMP documentation and are familiar with deviations, CR, and CAPAs. Experience with single-use technologies, aseptic processing, or customer-facing responsibilities will be considered an advantage.

Beyond your technical experience, strong communication and collaboration skills are important. You will work with both internal and external stakeholders, coordinating tasks and deliverables across departments such as Process Transfer, Process Validation, Engineering, QA, and QC.

We are also looking for someone with demonstrated experience in leading troubleshooting efforts who brings a self-motivated, organized, and proactive approach to their work.

Your Application & Our Interview Process

Submit your application no later than Wednesday, October 21.

We review applications as they are received and will conduct two rounds of interviews with qualified candidates during weeks 44 to 47, aiming for a start date on January 1.

We look forward to hearing from you!

**Who We Are

**AGC Biologics is a global Contract Development and Manufacturing Organization with a strong presence in Denmark. From our Søborg site, we develop and manufacture life‑changing advanced biologics for some of the world’s most innovative pharmaceutical companies. Together with our team members across Europe, the U.S., and Japan, we deliver development and manufacturing of mammalian and microbial-based therapeutic proteins, plasmid DNA (pDNA), messenger RNA (mRNA), viral vectors, and genetically engineered cells therapies. Across our global network, we are united by one mission: To work side by side with our customers in order to improve patients’ lives by bringing new biopharmaceuticals to market.

Posting text belongs to the employer. Removal requests: contact us.

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