Quality Control Specialist Analytical methods, Protein

11 hours ago

Uppsala, Uppsala, Sweden Q-Med AB Full time 80,000 - 120,000 per year

Location: Uppsala

Employment type: Full-time

Join Galderma, a leading global dermatology company with a strong international presence and a commitment to innovation, collaboration, and excellence. We offer exciting opportunities for personal and professional development in a dynamic and purpose-driven environment.

The Role

We are seeking a Quality Control Specialist - Analytical Methods, Protein to join our Quality Control (QC) organization. In this senior expert role, you will act as the technical authority in protein-based analytical methods, providing guidance, training, and scientific support to QC colleagues, cross-functional departments, and Galderma's global network. You will ensure analytical methods and laboratory practices comply with GMP and internal quality standards, lead method validations, and drive continuous improvement and optimization within your area of expertise. This position offers an exciting opportunity for an experienced professional with deep technical knowledge and a passion for analytical excellence and quality.

Key Responsibilities

  • Serve as Subject Matter Expert (SME) in analytical methods for proteins, including chromatographic, electrophoretic, and spectroscopic techniques.
  • Provide technical leadership, training, and mentorship to QC analysts and cross-functional partners.
  • Lead and coordinate method validations, including design, execution, evaluation, and reporting.
  • Ensure analytical methods and QC operations comply with GMP, GxP, and Galderma quality standards.
  • Identify, assess, and mitigate quality and compliance risks; support investigations with technical expertise.
  • Represent QC in cross-functional and global projects, providing analytical insights and recommendations.
  • Drive continuous improvement and simplification of analytical methods, work instructions, and quality systems.
  • Prepare and present technical documentation and reports for audits, inspections, and internal/external stakeholders.
  • Contribute to a positive, compliant, and collaborative laboratory culture.

Your Profile

Education:

  • PhD or Master's degree (or equivalent) in Biochemistry, Biotechnology, or a related field.

Experience:

  • Minimum 10 years of experience in Quality Control or R&D with a focus on protein analytical methods.
  • Extensive laboratory experience in chromatographic, electrophoretic, or spectroscopic analysis of proteins (e.g., SE, SEC-HPLC, SDS-PAGE, Western Blot).
  • Strong knowledge of method development, optimization, and validation.
  • Documented experience with GxP, GMP, and regulatory requirements for pharmaceuticals and/or medical devices.
  • Proven ability to train, coach, and explain complex analytical concepts to internal and external audiences.

Skills:

  • Advanced problem-solving and project management abilities.
  • Strong communication and presentation skills in English and Swedish (both written and spoken).
  • Ability to work independently and collaboratively in a global, cross-functional environment.

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