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Qualified Person/QP
Eingestellt von Progressive aus Düsseldorf
Projektbeschreibung
Please contact Deborah Toby at Progressive Pharma - 0207 469 5255
The role will require the QP to work on site for between 1-2 days per week and it will be an immediate start.
The duties of the role include:
- Auditing of API's and manufacturing and assembly sites,
- SOP's
- Product Quality Review
- Resolve technical issues
- Dossier submission
- Product release over EU
- Ensure compliance to MHRA regulations
Candidates must have the following skills:
- Experience releasing solid doses and Sterile's
- Eligible to act as a QP under Permanent Provisions
- Experience working in high volume fast paced environments
Candidates must be immediately available as this is an urgent role.
If you possess the necessary skills and experience, please send an updated CV and get in contact with Deborah Toby at and 0207 469 5255.
Keywords: Quality Assurance, QA, Quality audit, steriles, dosage forms, manufacturing, south east, liquid dose, Qualified Person, QP, QC, GMP, FDA. MHRA, Head of quality, Quality Manager, GCP, GxP, SOP, compliance, EU, guidelines, midlands, east midlands, QP, Qualified Person, IMP, Investigational Medicinal Products, batch, QMS, contract
To find out more about Progressive Recruitment please visit www.progressiverecruitment.com
Projektdetails
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Einsatzort:
London, Vereinigtes Königreich
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Projektbeginn:
asap
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Projektdauer:
Keine Angabe
- Vertragsart:
-
Berufserfahrung:
Keine Angabe
Geforderte Qualifikationen
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Kategorie:
Sonstiges