Quality Consultant - Process Validation & GMP (m/f/d)

EFOR

Frankfurt

Vor Ort

EUR 65.000 - 90.000

Vollzeit

14 Tage+
Bewerbungsgenerator

Hebe dich für diese Rolle von der Masse ab — erstelle in etwa einer Minute einen maßgeschneiderten Lebenslauf und ein Anschreiben.

Schaffe es an den ATS-Filtern vorbei

Zusammenfassung

EFOR, a leading Life Sciences consulting company, seeks a Quality Consultant – Process Validation & GMP (m/f/d) to join our German team in Frankfurt. You will review validation and process documentation, support GMP compliance, and collaborate with Quality, Manufacturing, MSAT and Validation teams on audits and continuous improvement.

The ideal candidate holds a degree in Pharmacy, Biotechnology, Chemistry, Life Sciences, or Engineering, with experience in QA, validation, CQV or quality systems

Qualifikationen

  • Degree in pharmacy, biotech, chemistry, life sciences, engineering or related.
  • Experience in Quality Assurance, Validation, CQV or Quality Systems in pharma.
  • Strong GMP knowledge and pharmaceutical quality systems.
  • Experience with validation documentation, deviations, CAPAs and change controls.
  • Experience in sterile manufacturing, biologics or injectables is an advantage.
  • Strong analytical and problem-solving and communication skills.

Aufgaben

  • Review and approve validation and process documentation.
  • Support GMP compliance initiatives and quality improvement programs.
  • Participate in deviation, CAPA and change control activities.
  • Ensure compliance with internal procedures and regulatory requirements.
  • Collaborate with Quality, Manufacturing, MSAT and Validation teams.
  • Support inspection readiness activities and audits.
  • Contribute to continuous improvement and quality excellence initiatives.

Kenntnisse

GMP knowledge
QA & Validation
Stakeholder mgmt
Analytical skills
Communication
English proficiency

Ausbildung

Related degree

Jobbeschreibung

Quality Consultant - Process Validation & GMP (m/f/d)

EFOR is one of Europe's leading Life Sciences consulting companies, supporting major pharmaceutical and biotechnology clients across engineering, CQV, validation, quality, manufacturing and digital transformation projects.

To strengthen our German team, we are looking for a Quality Consultant – Process Validation & GMP (m/f/d) who is passionate about quality, compliance and validation within GMP-regulated pharmaceutical environments.

Your Responsibilities
  • Review and approve validation and process documentation
  • Support GMP compliance initiatives and quality improvement programs
  • Participate in deviation, CAPA and change control activities
  • Ensure compliance with internal procedures and regulatory requirements
  • Collaborate with Quality, Manufacturing, MSAT and Validation teams
  • Support inspection readiness activities and audits
  • Contribute to continuous improvement and quality excellence initiatives
Your Profile
  • Degree in Pharmacy, Biotechnology, Chemistry, Life Sciences, Engineering or a related discipline
  • Professional experience in Quality Assurance, Validation, CQV or Quality Systems within the pharmaceutical industry
  • Strong knowledge of GMP requirements and pharmaceutical quality systems
  • Experience with validation documentation, deviations, CAPAs and change controls
  • Experience in sterile manufacturing, biologics or injectable products is an advantage
  • Strong analytical and problem-solving skills
  • Excellent communication and stakeholder management abilities
Languages
  • English: Professional proficiency required
  • German: Advantageous
What We Offer
  • A key role within one of Europe's fastest-growing Life Sciences consultancies.
  • Opportunity to actively shape the growth of EFOR in Germany and the DACH region.
  • International working environment with colleagues across Europe.
  • Extensive onboarding and continuous training on technical Life Sciences topics.
  • High level of autonomy and ownership.
About EFOR

Founded in 2013, EFOR has grown into one of Europe's leading Life Sciences consulting companies. Today, we are present across 3 continents, employ more than 3,200 consultants, generate €400 million in annual revenue, and continue our international expansion with the ambition of becoming the world's leading Life Sciences consultancy.

Ready to Join Us?

Become part of our growing German team and help us deliver some of the most exciting Life Sciences projects across Europe.

Hol dir deinen kostenlosen, vertraulichen Lebenslauf-Check.
oder ziehe deine Datei hierhin.
Similar jobs

Ähnliche Jobs, die dir auch gefallen könnten

Production / QC CPV Consultant Pharma (m/f/d)
Production / QC CPV Consultant Pharma (m/f/d)

EFOR • Frankfurt

Vor Ort
EUR 70.000 - 90.000
Equipment Requalification Consultant Pharma (m/f/d)
Equipment Requalification Consultant Pharma (m/f/d)

EFOR • Frankfurt

Vor Ort
EUR 70.000 - 110.000
Onboarding and training
Autonomy and ownership
International environment
MSAT / CPV Consultant Pharma (m/f/d)
MSAT / CPV Consultant Pharma (m/f/d)

EFOR • Frankfurt

Vor Ort
EUR 70.000 - 110.000
Key role in Europe expansion
International working environment
Extensive onboarding and continuous培训
Senior C&Q Coordination Lead (m/f/d)
Senior C&Q Coordination Lead (m/f/d)

EFOR • Frankfurt

Vor Ort
EUR 120.000 - 150.000
Manufacturing Data Remediation Consultant Pharma (m/f/d)
Manufacturing Data Remediation Consultant Pharma (m/f/d)

EFOR • Frankfurt

Vor Ort
EUR 65.000 - 95.000
Visual Inspection Consultant Pharma (m/w/d)
Visual Inspection Consultant Pharma (m/w/d)

EFOR • Frankfurt

Vor Ort
EUR 70.000 - 95.000
Internationales Arbeitsumfeld
Weiterbildungsmöglichkeiten
Umfassendes Onboarding
+1
(Senior) Consultant Qualification & Validation
(Senior) Consultant Qualification & Validation

Arcondis Group • Eschborn

Hybrid
EUR 90.000 - 130.000
Director, Quality Assurance
Director, Quality Assurance

LabConnect • Köln

Vor Ort
EUR 120.000 - 180.000
Remote workdays
Career growth
Equal opportunity employer
Junior GMP Qualification Engineer Pharma (m/w/d)
Junior GMP Qualification Engineer Pharma (m/w/d)

Full-Time • Deutschland

Vor Ort
EUR 50.000 - 70.000
30 Tage Urlaub
Betriebliche Altersvorsorge
Diensthandy
+1
Senior Quality Systems Architect (m/f/d)
Senior Quality Systems Architect (m/f/d)

CHEPLAPHARM • Binningen

Hybrid
EUR 90.000 - 120.000
International team
Flexible working
Company pension
+2