Despatch Quality Control Inspector - Dresden, Deutschland - PCI Pharma Services

PCI Pharma Services
PCI Pharma Services
Geprüftes Unternehmen
Dresden, Deutschland

vor 4 Tagen

Lena Wagner

Geschrieben von:

Lena Wagner

beBee Recruiter


Beschreibung
Life changing therapies. Global impact. Bridge to thousands of biopharma companies and their patients.

We are PCI.

Our investment is in People who make an impact, drive progress and create a better tomorrow. Our strategy includes building teams across our global network to pioneer and shape the future of PCI.

  • Department: _
  • Quality_
  • Reporting to_: Manager Quality Control
  • Responsible for (staff)_: NA
  • General Purpose of Role_:
  • To assure the quality of clinical trials distribution.
  • Main Responsibilities_:
  • Ensuring that all activities are carried to GMP and GDP.
  • Performing the post pick verification of Clinical Trial shipments to ensure that the appropriate supplies have been picked and have been prepared ready for despatch correctly.
  • Performing the verification that temperature controlled shipments (e.g cold chain, frozen) have been configured correctly including the activation of temperature monitoring devices.
  • Inspections of pick and pack cubicles or areas before materials or products are introduced to ensure the absence of materials or products from previous operation.
  • Quality oversight of all point of dispatch labelling.
  • Perform spot checks of warehouse log books to ensure accuracy and compliance with Good Documentation Practice.
  • Cross functional support with the QC inspector role
  • Assisting QA with the investigation of customer complaints and deviations.
  • Outcomes of Role_:
  • Reduced number of incorrect shipments or despatch errors
  • Drive towards right first time approach with warehouse operators
  • Previous Work Experience_:
  • A distribution/warehouse environment
  • A GMP environment.
- experience within a quality role, is desirable

  • Specific Knowledge / Skills Competence_:
  • A high level of attention to detail is essential for the successful outcome of this role
  • Experience in the clinical supply field,
  • An understanding of Quality Standards including GMP, GCP and GDP.
  • Knowledge of Sage 200 or similar enterprise management systems
  • IT literate in standard packages (MS Office)
  • Good written and communication skills in English and German
Join us and be part of building the bridge between life changing therapies and patients.

Let's talk future


Equal Employment Opportunity (EEO) Statement:

  • PCI Pharma Services is an Equal _
  • Opportunity/Affirmative_
  • Action Employer. We do not unlawfully discriminate on the basis of race, color, religion, age, sex, creed, national origin, ancestry, citizenship status, marital or domestic or civil union status, familial status, affectional or sexual orientation, gender identity or expression, genetics, disability, military eligibility or veteran status, or any other protected status._

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