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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
  • Minimum 3 years laboratory experience
  • Operating state-of-the-art laboratory equipment
  • Capability for laboratory work and microscopic evaluation (mandatory)
  • Willingness to work in clean rooms (up to ISO 5)
  • Fluent English & German (written and spoken)
  • Collaboration and teamwork ability
  • Advanced project management skills
  • In-depth experimental skills for testing routines
  • Strong project ownership mindset and motivation
  • Excellent GMP compliant documentation skills
  • Very good verbal and written communication skills
  • Structured, independent work approach
  • Thinking outside the box attitude
  • Enjoyment of constructive technical discussions
  • Solution-oriented, problem-solving mentality
  • Willingness to learn and develop
  • Flexibility for early/late shifts
  • Good experimental and lab organizational skills
  • Safe handling of measurement technologies/techniques
  • Reliability, diligence, flexibility
  • Microsoft Office software experience
  • SAP and Minitab experience (plus)
  • Ability to stand in laboratory environment
  • Manual dexterity for operating tools/controls
  • Mental skills: communication, decision-making, data interpretation, reading/writing

Tasks

  • Develop methods for release testing and in-process control.
  • Optimize methods for release testing and in-process control.
  • Validate methods for release testing and in-process control.
  • Collaborate with international teams to implement methods.
  • Train users on developed methods.
  • Support global laboratory teams.
  • Contribute to global laboratory joint projects.
  • Manage small and mid-size global projects.
  • Plan small and mid-size projects.
  • Track progress for small and mid-size projects.
  • Report on small and mid-size projects.
  • Communicate project updates for small and mid-size projects.
  • Adhere to ESOPs, SOIs, and PFNBs.
  • Ensure compliance with cGMP regulations.
  • Author lab study protocols for method development.
  • Execute lab study protocols for method development.
  • 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.
  • Perform literature searches on guidelines, publications, and equipment.
  • Assist SMEs with deviation and out-of-spec investigations.
  • Support the implementation of global change controls.
  • Ensure compliance with safety regulations.

Work Experience

3 years

Education

Bachelor's degree

Languages

EnglishBusiness FluentGermanBusiness Fluent

Tools & Technologies

Laboratory equipmentMeasurement technologiesMicrosoft OfficeSAPMinitab

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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