Job Description Summary
Supports all activities within the assigned Quality department. Contributes to the implementation, maintenance, and execution of the assigned Quality and/ or Laboratory Systems in an effective and compliant manner.
Job Description
Sample storage and management.
Analytical testing and documentation of API / drug substance / drug product / finished product / Complaints / stability / packaging material samples
Ensure all activities in compliance with cGxP, incl. data integrity
Stability (when not centralized)
Testing/Sample storage and management
Analytical documentation of stability samples to cGxP standards
Detect and report potential accident, risks and propose solutions
Essential Requirements:
Preferred: Previous experience working in a laboratory environment in the pharmaceutical industry (quality assurance, production), aseptic technique.
Administrative activities and GMP and HSE-compliant, efficient production and documentation of standardized tasks in the infrastructure
Breakthrough Analysis; Being Resilient; Operational Excellence; Continuous Learning; Digital & Tech Savvy
Laboratory equipment; Quality Control (QC) Testing; Quality Control Sampling; knowledge of TQM and related industry GxP standards and processes; Laboratory Excellence; Quality decision making
Desirable Requirements:
University degree or equivalent experience in Pharmacy or Chemistry or equivalent + 0-4 years working experience
Skills Desired
Collaboration, Communication Skills, Data Integrity, Deadline Adherence, Dealing With Ambiguity, Decision Making, Digital saviness, Leadership, Problem Solving Skills, Regulatory Requirements knowledge