Quality Inspector (m/f/d) Goods Receipt at WEST PHARMACEUTICAL SERVICES INC
BERLIN, Berlin, Germany -
Full Time


Start Date

Immediate

Expiry Date

03 Jan, 27

Salary

90000.0

Posted On

05 Oct, 26

Experience

4 year(s) or above

Remote Job

Yes

Telecommute

Yes

Sponsor Visa

No

Skills

Industry

Pharmaceutical Manufacturing

Description

Key duties and responsibilities

  • Sampling according to sampling plan
  • Forwarding of samples of raw materials, supplies and operating materials to the appropriate department
  • Testing of bags and films (dimensions, tensile strength, etc.)
  • Color and reactivity testing of raw materials
  • Documentation and filing of test results
  • Booking and release of raw materials as well as monitoring of testing/measuring equipment
  • Handling supplier complaints
  • Handling of OOS, deviations and process changes
  • Creation of data analyses

Training

  • Successfully completed technical training

Professional experience

  • Professional experience in a comparable position, preferably in the pharmaceutical sector or with GMP experience.
  • Experience in quality assurance

Preferred knowledge, skills and abilities

  • Security in the use of Microsoft Office products (Word, Excel) and SAP
  • Independent, structured and self-reliant work style
  • Knowledge of GMP-compliant working methods and DIN ISO 9001
  • Good English skills, both spoken and written.
  • Strong organizational skills and a very precise and meticulous work ethic
  • Driving licence class B


How To Apply:

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Responsibilities

Key duties and responsibilities

  • Sampling according to sampling plan
  • Forwarding of samples of raw materials, supplies and operating materials to the appropriate department
  • Testing of bags and films (dimensions, tensile strength, etc.)
  • Color and reactivity testing of raw materials
  • Documentation and filing of test results
  • Booking and release of raw materials as well as monitoring of testing/measuring equipment
  • Handling supplier complaints
  • Handling of OOS, deviations and process changes
  • Creation of data analyses

Training

  • Successfully completed technical training

Professional experience

  • Professional experience in a comparable position, preferably in the pharmaceutical sector or with GMP experience.
  • Experience in quality assurance

Preferred knowledge, skills and abilities

  • Security in the use of Microsoft Office products (Word, Excel) and SAP
  • Independent, structured and self-reliant work style
  • Knowledge of GMP-compliant working methods and DIN ISO 9001
  • Good English skills, both spoken and written.
  • Strong organizational skills and a very precise and meticulous work ethic
  • Driving licence class B


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