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Job
Firma
Efor Lyon - Efor Group SAS
Position
CQV Professionals (Lead / Senior / Engineer) (m/f/d)
Ort
Deutschland, Hessen

Beschreibung

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Firma: EFOR

UNTERNEHMENS-ID: 3234841
Stellenausschreibungs-URL: https://de.linkedin.com/jobs/view/cqv-professionals-lead-senior-engineer-m-f-d-at-efor-4434118285?position=5&pageNum=15&refId=8xiek0%2FvmC9zr1SOivFJ1Q%3D%3D&trackingId=bPApoOYWKh0sq35NXSh51Q%3D%3D

Karrierestufe

Management

Beschäftigungsverhältnis

Vollzeit

Tätigkeitsbereich

Ingenieurwesen, Qualitätssicherung und Projektmanagement

Branchen

Arzneimittelherstellung und Biotechnologieforschung
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CQV Professionals (Lead / Senior / Engineer)

Location: Hesse Region, Germany (Hybrid / On-site depending on project phase)

Join Exciting Pharmaceutical & Biotech Projects

EFOR is supporting several large-scale pharmaceutical and biotechnology projects across Germany. We are currently expanding our CQV (Commissioning, Qualification & Validation) team and are looking for experienced professionals to join upcoming GMP manufacturing projects in the Hesse region.

Whether you are an experienced Workstream Lead or a hands-on CQV Engineer, we would be pleased to hear from you.

We are currently looking for professionals with experience in one or more of the following areas:
C&Q Workstream Leads
Upstream Processing (USP)
Downstream Processing (DSP)
Buffer Area / Tank Farm
Clean Utilities (WFI, Clean Steam, CIP/SIP)
Cleanrooms / HVAC / Facilities
QC Equipment & COTS (Commercial Off-The-Shelf Equipment)
Automation
Documentation & KNEAT
CQV Documentation Specialists
URS / DQ / IQ / OQ / PQ documentation
Protocol authoring
Risk Assessments
RTM
GMP documentation lifecycle
KNEAT / ValGenesis / Veeva Vault experience is highly desirable
CQV Execution Engineers
Commissioning
FAT / SAT
IQ / OQ / PQ execution
Equipment Qualification
Utilities Qualification
Cleanroom Qualification
GMP manufacturing facilities

What we are looking for
Experience within the pharmaceutical, biotechnology or life sciences industry
Strong GMP knowledge
Commissioning, Qualification & Validation (CQV) experience
Experience in documentation preparation and/or execution activities
Experience with biologics, sterile manufacturing or drug substance facilities is an advantage
Strong communication skills and the ability to work in multidisciplinary international teams

What we offer
Opportunity to work on large-scale pharmaceutical manufacturing projects
Long-term project opportunities
International project environment
Competitive compensation
Career development within EFOR Group
Collaboration with leading life sciences companies

Language
English is required.
German is an advantage but is not mandatory.

If you are interested in discussing current or upcoming opportunities, we would be happy to hear from you.

Please send us your updated CV together with your availability, mobility and salary expectations.
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Den Jobinserenten von EFOR direkt kontaktieren

Defne Pehlivanoğlu Yorulmaz Defne Pehlivanoğlu Yorulmaz Talent Acquisition @EFOR
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