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WEWest Pharmaceutical Services

Specialist, Global Laboratory(m/w/x)

Stolberg
Full-timeOn-siteExperienced

Method development and validation for injectable medicine release testing at a pharmaceutical supplier, including microscopic evaluation in ISO 5 clean rooms. Minimum 3 years lab experience and microscopic evaluation capability required. International team collaboration, work in ISO 5 clean rooms.

Requirements

  • Bachelor’s degree in Natural Sciences or equivalent experience
  • At least 3 years hands-on laboratory experience
  • Experience in operating state-of-the-art laboratory equipment
  • Mandatory capability for laboratory work and microscopic evaluation
  • Willingness to work in clean rooms (up to ISO 5)
  • Fluent English and German (written and spoken)
  • Collaboration and teamwork ability
  • Advanced project management skills
  • In-depth experimental skills for selected testing routines
  • Strong project ownership mindset and motivation
  • Excellent GMP compliant documentation skills
  • Very good verbal and written communication skills
  • Structured and independent working style
  • Thinking outside the box attitude
  • Enjoyment of constructive technical discussions
  • Solution-oriented and problem-solving mentality
  • Willingness to learn and develop
  • Flexibility for early or late shifts
  • Good experimental and lab organizational skills
  • Safe handling of measurement technologies/techniques
  • Reliability, diligence, and flexibility
  • Experience in Microsoft Office software package
  • Experience in SAP and Minitab (plus)
  • Availability up to 52 business days per year
  • Physical activity: standing in laboratory environment
  • Physical activity: using hands to finger, handle, feel, operate objects/tools/controls, reach
  • Mental skills: communication, quick decision making, data interpretation, reading/writing, public speaking

Tasks

  • Follow relevant ESOPs, SOIs, and PFNBs
  • Plan small and mid-size projects
  • Track project progress
  • Report on project status
  • Communicate project updates
  • Author lab study protocols for method development
  • Execute lab study protocols
  • Analyze experimental results independently
  • Author and execute validation protocols
  • Author and execute qualification protocols for computerized inspection systems
  • Author and execute PNRs
  • Author, execute, and document inter-laboratory studies
  • Train trainers on new global test methods and technologies
  • Conduct literature searches for project-relevant information
  • Assist SMEs with deviation and out-of-spec investigations
  • Support the implementation of global change controls
  • Comply with all safety regulations

Work Experience

  • 3 years

Education

  • Bachelor's degree

Languages

  • EnglishBusiness Fluent
  • GermanBusiness Fluent

Tools & Technologies

  • Microsoft Office
  • SAP
  • Minitab

Benefits

Career Advancement

  • Professional growth opportunities
  • Leadership development

Learning & Development

  • Training programs
  • Skill certification initiatives

Additional Allowances

  • Tuition assistance

Social Impact

  • Volunteerism encouragement
  • Charitable programs

Bonuses & Incentives

  • Performance-based bonuses

Other Benefits

  • Service recognition
  • Employee appreciation initiatives
Find the original job posting in its most current version here. Nejo automatically captured this job from the website of West Pharmaceutical Services and processed the information on Nejo with the help of AI for you. Despite careful analysis, some information may be incomplete or inaccurate. Please always verify all details in the original posting! Content and copyrights of the original posting belong to the advertising company.

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