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AbbVie

Global biopharmaceutical company developing medicines

Laboratory Technician QC Medtech / Analyst 1

Inspection & TestPosted on Nov 9
Full-timeLudwigshafen, GermanyNo salary listedIn-person

About the Job

Requirements

  • Completed vocational training as a chemical or biological laboratory technician, pharmaceutical technician, or in a comparable technical, pharmaceutical, or natural-science field; alternatively, a comparable qualification and at least three years of relevant professional experience, preferably in the pharmaceutical industry and a GMP-regulated environment.
  • Knowledge of reading and applying standard operating procedures, testing procedures, and documentation requirements.
  • Knowledge of medical-device testing and experience working according to ISO 13485 and/or Good Manufacturing Practice (GMP).
  • Experience with sample collection, handling starting materials and samples, and GMP-compliant documentation.
  • A strong sense of responsibility and quality, reliability, commitment, and a careful and precise working style.
  • Initiative and the ability to carry out tasks independently, systematically, and on schedule.
  • Teamwork, communication, and cooperation skills.
  • Ability and willingness to collaborate constructively across departments with employees and other interfaces.
  • Willingness to continuously learn new processes, materials, testing methods, and systems.
  • Good written and spoken German and English, confident use of common Microsoft Office applications, and knowledge of SAP and Laboratory Information Management Systems (LIMS).

Responsibilities

  • Perform operational quality-control activities in Medical Technologies quality control according to applicable testing procedures, standard operating procedures, GMP, and ISO 13485 requirements.
  • Test and assess medical devices, materials, and samples, and document results completely, traceably, and in compliance with GMP.
  • Provide support to the sample collection area as needed, including sampling, labeling, processing, and forwarding starting materials and samples, as well as visually inspecting parenteral products.
  • Enter and maintain testing- and sample-related data in designated systems, particularly LIMS and SAP.
  • Collaborate with adjacent departments and interfaces, and contribute to handling deviations and continuous improvement within the area of responsibility.

Desired Qualifications

  • Relevant professional experience in the pharmaceutical industry and a GMP-regulated environment is preferred.

About the Company

AbbVie

Global biopharmaceutical company developing medicines

AbbVie is a global biopharmaceutical company that develops and sells medicines to treat serious health conditions. Its portfolio spans immunology, oncology, virology, neuroscience, and aesthetics, with products designed to modulate the immune system, target disease pathways, or support medical aesthetics. AbbVie compounds its products through a heavy emphasis on research and development, investing billions to build a steady pipeline of new therapies. Its medicines are brought to market by selling to healthcare providers, hospitals, and clinics, and in some cases directly to patients via prescriptions. The company differentiates itself through a wide, globally distributed product line, substantial R&D investment, and a commitment to sustainability and patient care, including science-based targets. AbbVie’s goal is to improve patient outcomes by delivering effective treatments for unmet medical needs while pursuing long-term, responsible growth across healthcare markets.

Company size
10,001+
Company stage
IPO
Headquarters
North Chicago, IL
Founded
1888

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