Pharma Deviation Handling Team Lead

Fujifilm

Hillerød

Hybrid

DKK 900,000 - 1,200,000

Full time

9 days ago

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Benefits offered by this job

Remote work 1 day/week

Job summary

Fujifilm Biotechnologies Denmark seeks an Associate Manager to lead the Deviation Handling Team in Drug Product and Finished Goods. You will balance people leadership with hands-on investigations, guiding root-cause analyses and ensuring effective CAPAs while coordinating with production, quality, and external stakeholders.

You will be the bridge for customer and auditor relations, ready to present findings during audits and inspections, maintaining stringent compliance in a fast-paced

Qualifications

  • Bachelor’s or Master’s degree in a science-related field.
  • Minimum 5 years in a cGMP pharmaceutical manufacturing environment.
  • Proven leadership in a management or team lead role.
  • Strong verbal and written communication for external customers/auditors.
  • Ability to manage high-pressure investigations and CAPA activities.

Responsibilities

  • Lead and mentor the Deviation Handling Team in drug product and finished goods.
  • Directly investigate high-severity deviations and ensure robust root-cause analysis.
  • Collaborate with Production, Engineering, and Science to implement CAPAs.
  • Serve as primary contact for deviation-related customer queries and audit presentations.

Skills

Team leadership
Root-cause analysis
Cross-functional collaboration
Communication
Investigations

Education

Bachelor’s or Master’s in Pharmacy, Chemistry, Engineering, Biology

Job description

Fujifilm Biotechnologies Denmark seeks an Associate Manager to lead the Deviation Handling Team in Drug Product and Finished Goods. You will balance people leadership with hands-on investigations, guiding root-cause analyses and ensuring effective CAPAs while coordinating with production, quality, and external stakeholders.

You will be the bridge for customer and auditor relations, ready to present findings during audits and inspections, maintaining stringent compliance in a fast-paced

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