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39 experts


Patent Drafting Formulation development Technology transfer ANDA Regulatory affairs

An experienced Pharmaceutical Scientist with about 12+ years of research experience of Pharmaceutical MNCs with a track record of success. Developed many innovative but cost-effective, stable and

Head R&D | Team Leader | BASF Pharma Application Lab | Reseach Scientist | Research Trainee
Doctor of Philosophy (PhD) Pharmaceutical Sciences | PG Diploma in Regulatory Affairs Regulatory Affairs | Masters of Ph ...

Business Development Manager

Villeroy, France
management Solution Selling Business Strategy Project Management Account Management
Track and Trace I Business Development Manager, I Life Sciences I Europe | CAC 40 Strategic Account Sales Manager | VALIPOST ...
Systemic approach Sciences de l'Art Political Economy, Sociology | ENSAAMA Master's Degree Industrial and Product Design ...
Villeroy, France

Interim manager

Mechelen, Belgium
Pharmaceutical Industry Change Control Lifesciences Manufacturing Technology transfer
Supply Chain Management Leader EuAFME-CLAR-US exports | Supply & Logistics Operations Leader EuAfME | Manager Aseptic Manufac ...
Certified Supply Chain Professional | Middle Management Course General fields of management | Bio-Ingenieur in de Schei ...
Mechelen, Belgium

RA Manager CMC, Vendor Manager

Research Cell Culture GMP CMC Regulatory Affairs Analytical Method Validation
Regulatory Affairs Manager CMC and Vendor Manager | Pharmaceutical Chemical Expert | Entrepreneur | Project Manager | Design ...
Doctor of Philosophy (PhD) Biochemistry | Master of Science (MSc) Biochemistry | Matriculation Exam

Quality Assurance & Regulatory Affairs Manager

United Kingdom
R&D GMP Microbiology Validation Pharmaceutical Industry
Quality Assurance and Regulatory Affairs Manager | Director | R&D Director | R&D Group Manager | Principal Scientist
Ph.D. Pharmacy | M.Sc. Quality Management | B.Sc. (Honours) Food Science
United Kingdom

Quality manager

Ameide, Nederland
Quality Assurance (QA)

Experienced Professional in the field of Regulatory Affairs & Quality Assurance & Approbation of medical devices class IIa and ISO 9001:2008.

Owner / Manager QA/RA & Certified Lead Auditor ISO 13485 | Quality Assurance Manager a.i. | Business Controller / Manager QA ...
Lead Auditor ISO 13485 | Bachelor of Science (BS) Bedrijfseconomie | student ASCO I | VBO VBO - Motorvoertuigentechniek ...
Ameide, Nederland

Quality Assurance

Toronto, ON, Canada
ANDA SOP GMP Validation Regulatory affairs

Worked in previous job as Senior Auditor – Asia Pacific in Astra Zeneca Pharma India Limited, responsible for audits of Astra Zeneca manufacturing sites and R&Ds, supplier audits (API, Excepient

QA / QC Associate | Senior GMP Auditor - Asia Pacific | Senior Manager-Global Quality | Asst. Manager-Quality Assurance | Exe ...
Post Graduate Diploma Pharmaceutical Regulatory Affairs | M.Pharm Natural Products | Bachelors in Pharmaceutical Science ...
Toronto, ON, Canada

Senior Consultant / Interim Manager

Lichtaart, Kasterlee, Belgium
GMP Validation Change Control V&V Pharmaceutical Industry
Senior consultant - Analytical Technical Integrator | Senior consultant - PDMS Lifecycle Management & Specifications | Interi ...
Master in the chemistry - biochemistry | Master Biochemistry
Belgium | Nederland | Lichtaart, Kasterlee, Belgium

BioPharma Project Manager

Lisbon, Portugal
Biotechnology molecular biology Lifesciences In Vivo Drug Development
Project Manager | Operations Officer | Research Scientist and Project Coordinator | Drug development
PhD Gene Therapy | Pos-graduation Cell Biology | B.Sc. Biochemistry
Lisbon, Portugal

Fayez Abou Hamad, MD Vigilance Expert – Pharmacist – Complaint & Vigilance Manager

Heppen, Leopoldsburg, Belgium
Pharmaceutical Industry Medical Devices
MD Vigilance Expert – Pharmacist – Complaint & Vigilance Manager | Document Analyst – Responsible Clinical Evidence ...
Master Pharmaceutical Sciences
Heppen, Leopoldsburg, Belgium
39 experts

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