Downstream Scientist (Manufacturing, On-site)

Copenhagen, Capital Region
Posted 1 week ago
Engineering

About the role

Job summary

This role involves supporting drug production as a Downstream Scientist within the Manufacturing Product Support department. The position requires technical problem-solving skills and experience in a cGMP environment, focusing on batch documentation, deviation handling, and ensuring timely production execution.

Qualifications

  • Bachelor’s or Master’s degree in natural or life sciences preferred.
  • Minimum of 2 years of experience in a manufacturing team under cGMP, preferably in the pharmaceutical industry.
  • Experience in a production support role with downstream process knowledge is advantageous.
  • Familiarity with GMP documentation, deviations, and quality processes (CRs, CAPAs) is preferred.

Responsibilities

  • Create and review Master Production Records.
  • Facilitate solutions during batch execution breakdowns.
  • Ensure timely closure of deviations and quality documents.
  • Act as a customer meeting representative and support audits and inspections.
  • Participate in continuous improvement initiatives.
  • Provide on-call support approximately 24 hours three times a month.

Skills

  • Strong communication skills for interaction with stakeholders.
  • Ability to coordinate multi-departmental tasks and deliverables.
  • Demonstrated experience in troubleshooting and problem-solving.
  • Self-motivated, organized, and proactive work ethic.

Education

  • BSc or MSc in a relevant field preferred.

Tools

  • Experience with single-use technologies and aseptic processing is a plus.
Full Access

Ready to apply for this role?

Full Access gives you the company name, full job description, and a direct link to apply. On the 1- and 3-month plans, CV Tailor rewrites your CV for this exact role.

Share this job