Quality Systems Lead: Complaint & Recall Management

Zealand Pharma

Søborg

On-site

DKK 700,000 - 950,000

Full time

14 days+
Application generator

Get a reply from this employer — a resume and cover letter tailored to exactly what they’re hiring for.

Get past ATS filters

Job summary

Zealand Pharma A/S in Denmark is seeking an QA Manager for complaint management to lead and optimize our complaint handling across clinical and marketed products, collaborating with Manufacturing QA, the CMC organization, CMOs and partners.

The role combines hands‑on complaint processing with process ownership and continuous improvement of the quality systems supporting complaint handling, including Veeva Quality Vault.

Qualifications

  • Quality-minded, collaborative professional with strong compliance judgment.
  • Ability to build trusted relationships.
  • Experience in life science industry.
  • Experience with complaint processing of drugs, medical devices, and/or drug-device combinations.
  • Solid understanding of GMP and Quality Systems.

Responsibilities

  • Building and strengthening complaint competencies internally.
  • Complaint management, incl. support, coordination and contact with stakeholders.
  • Collaborate with Manufacturing QA, CMOs, Partners and cross-functional stakeholders on complaint-related matters.
  • Maintain and continuously improve complaint and recall processes, including procedures, templates, training, and ways of working.
  • Manage recall (and mock recalls) related activities.
  • Contribute to development and optimization of Veeva Quality Vault and related complaint management processes.
  • Support the use of quality data, reporting, and trending to drive continuous improvement.

Skills

Quality management
GMP knowledge
Stakeholder communication
Travel willingness
Quality systems

Education

Master's degree in life science

Tools

Veeva Vault

Job description

Zealand Pharma A/S in Denmark is seeking an QA Manager for complaint management to lead and optimize our complaint handling across clinical and marketed products, collaborating with Manufacturing QA, the CMC organization, CMOs and partners.

The role combines hands‑on complaint processing with process ownership and continuous improvement of the quality systems supporting complaint handling, including Veeva Quality Vault.

Get your free, confidential resume review.

or drag and drop your file here.

Similar jobs

Similar jobs worth comparing

QA Manager
QA Manager

Zealand Pharma • Søborg

On-site
DKK 700,000 - 950,000
Senior QA Manager: GLP/GCP Audit & Compliance Lead
Senior QA Manager: GLP/GCP Audit & Compliance Lead

Zealand Pharma • Søborg

On-site
DKK 900,000 - 1,300,000
Associate QA Director, Drug Product & CMO Compliance
Associate QA Director, Drug Product & CMO Compliance

Zealand Pharma A/S • Gladsaxe Kommune

On-site
DKK 1,200,000 - 1,800,000
Associate QA Director, Drug Product & CMO Oversight
Associate QA Director, Drug Product & CMO Oversight

Zealand Pharma • Søborg

On-site
DKK 900,000 - 1,250,000
Associate QA Director, Manufacturing QA
Associate QA Director, Manufacturing QA

Zealand Pharma • Søborg

On-site
DKK 900,000 - 1,250,000
Senior QA Manager - GCP/GMP & Regulatory Leader
Senior QA Manager - GCP/GMP & Regulatory Leader

LINK Medical Research AS • København

On-site
DKK 673,000 - 972,000
Competitive compensation
Benefits scheme
Senior QA Manager
Senior QA Manager

Zealand Pharma • Søborg

On-site
DKK 900,000 - 1,300,000
Senior QA Lead: Drug Substance & Biologics
Senior QA Lead: Drug Substance & Biologics

Genmab • København

On-site
DKK 608,000 - 912,000
Pension
Health insurance and wellness benefits
Paid time off
+1
Associate QA Director, Manufacturing QA
Associate QA Director, Manufacturing QA

Zealand Pharma A/S • Gladsaxe Kommune

On-site
DKK 1,200,000 - 1,800,000
Global GCP Quality Advisor & Compliance Leader
Global GCP Quality Advisor & Compliance Leader

Cari • Søborg

Remote
DKK 743,000 - 1,092,000