Martillac, New Aquitaine, France
4 months ago

Job Overview

Job Type
Full-Time
Pay
Not disclosed

Job description

Location:
Martillac, New Aquitaine, France
Work arrangement:
On-site

Role Summary

Reporting to the Physical Chemistry Supervisor of the analytical QC laboratory, you will be responsible for carrying out analyzes as part of production support and product release. You will carry out these activities in accordance with Good Manufacturing Practices, in compliance with the Group's Quality Assurance rules and regulatory authorities.

Responsibilities

  • Management and physical/documentary monitoring of samples
  • Routine and qualification/validation analyses: HPLC, UHPLC, cIEF capillary electrophoresis, Optical Density, pH
  • Traceability and data integrity (DI, LIMS, maintenance, corrective/preventive actions)
  • Transcription of analytical results on time and verification of compliance
  • Maintenance and management of procedure type documentation
  • Management of the availability of reagents/consumables necessary for analyzes
  • Support for surveys and laboratory investigations
  • Compliance with EHS procedures and policies
  • Maintaining a safe working environment that complies with regulatory requirements

Requirements

Training and experience

  • Bac +2 minimum in Chemistry, Biochemistry or equivalent scientific discipline
  • Minimum 5 years of laboratory experience (biotechnology or pharmaceutical sector desired)
  • Mastery of laboratory techniques and analytical instruments
  • Logical and scientific reasoning
  • Knowledge of computerized systems (LIMS, Empower, etc.)
  • Rigor, team spirit and “customer” satisfaction oriented
  • Understanding of basic English desired for optimal use of the various laboratory tools.
  • Sense of organization/meticulous in documentation, monitoring, traceability/pro activity.
  • Good capacity for adaptation (technical and relational), sense of communication/respect for deadlines and ability to evolve in a changing environment
  • Schedules and organization
  • Shift work with punctual on-call duty.

Benefits

AbbVie is an equal opportunity employer and is committed to operating with integrity, driving innovation, transforming lives and serving our community.  Equal Opportunity Employer/Veterans/Disabled.

  • US & Puerto Rico only - to learn more, visit https://www.abbvie.com/join-us/equal-employment-opportunity-employer.html
  • US & Puerto Rico applicants seeking reasonable accommodation, click here to learn more:
  • https: //www.abbvie.com/join-us/reasonable-accommodations.html

About the Company

About AbbVie

AbbVie's mission is to discover and provide innovative therapies and solutions that address serious diseases today and meet the medical challenges of tomorrow. We strive to have a remarkable impact on the lives of patients in several major key therapeutic areas: immunology, ophthalmology, oncology, neuroscience and virology, as well as in aesthetic medicine with the products and services of our Allergan Aesthetics portfolio.

Role:
Physico-Chemistry Quality Control Laboratory Technician (F/M/X)
Industry Type:
Pharmaceuticals
Job Type:
Full-Time

Company profile

AbbVie Inc. is an American pharmaceutical company headquartered in North Chicago, Illinois. It produces drugs to treat a wide range of medical issues. The company ranks sixth on the list of largest biomedical companies by revenue, 77th on the Fortune 500 and 108th on the Forbes Global 2000. Its name combines Abbott, the name of its former parent company, with vie, intended as a reference to a Latin root meaning life.

Company Size
50,000 - 100,000 employees
Headquarters
North Chicago, Illinois, United States
Founded
2012
Funding Stage
Public

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