Quality Control Specialist Analytical Methods
Q-Med AB / Biomedicinjobb / Uppsala
2025-11-12
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hela Sverige 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 to join our Quality Control (QC) organization. In this expert-level role, you will act as the technical authority for analytical methods, providing scientific guidance, training, and support to QC colleagues, other departments, and Galderma's global network. You will ensure analytical methods and laboratory practices meet regulatory and internal quality standards, lead method validations, and drive continuous improvement and optimization within the analytical area. This role offers an exciting opportunity for a seasoned professional who enjoys solving complex challenges and influencing quality and compliance on a global scale.
Key Responsibilities
* Serve as Subject Matter Expert (SME) in analytical chemistry, with deep expertise in chromatographic techniques (e.g., HPLC, GC), including troubleshooting, method development, and validation.
* Provide technical leadership, coaching, and support to QC teams and cross-functional colleagues.
* Lead and coordinate method validations, including planning, execution, data evaluation, and authoring of validation reports.
* Ensure that analytical methods and QC operations comply with GMP and GxP requirements and Galderma standards.
* Identify, evaluate, and mitigate quality and compliance risks; contribute to deviation investigations with advanced technical insight.
* Represent QC in cross-functional and global projects, contributing expert knowledge and analytical perspective.
* Drive improvement initiatives using structured methodologies such as Quality Risk Management (QRM) and Lean/Yellow Belt tools.
* Prepare and present technical documentation, reports, and presentations for internal and external stakeholders, including auditors and regulatory authorities.
* Contribute actively to a positive, collaborative, and compliant laboratory culture.
Your Profile
• PhD or Master's degree (or equivalent) in Chemistry, Pharmaceutical Science, or a related field.
Experience:
* Minimum 10 years of experience in Quality Control or R&D, focusing on analytical method development and validation.
* Extensive experience with chromatographic methods and advanced analytical instrumentation.
* Proven understanding of GxP, GMP, and pharmaceutical and/or medical device regulations.
* Demonstrated ability to train, coach, and communicate technical concepts clearly to diverse audiences.
Skills:
* Strong analytical, problem-solving, and project management skills.
* Excellent communication and presentation abilities in Swedish and English (both written and spoken).
* Ability to work independently and collaboratively across teams and geographies.
Ersättning Not Specified
Så ansöker du Sista dag att ansöka är 2025-12-03
Klicka på denna länk för att göra din ansökan Arbetsgivarens referens Arbetsgivarens referens för detta jobb är "JR016062".
Omfattning Detta är ett heltidsjobb.
Arbetsgivare Q-Med AB (org.nr 556258-6882)
Arbetsplats Galderma
Kontakt Galderma
hanan.nur@galderma.com Jobbnummer 9601119