Job Details
Posted 19 September, 2026
Job Id: 630685
SME, GMP and Facility Expert – Uppsala, Sweden
Job Description
Join Our Team as an SME, GMP and Facility Expert – Uppsala, Sweden
Are you a seasoned professional with deep expertise in GMP, quality assurance, and facility management? This is your opportunity to make a significant impact in a dynamic environment dedicated to transforming cosmetic manufacturing into pharmaceutical-grade production. Based in Uppsala, Sweden, you will be at the forefront of supporting a leading client’s transition to compliant, high-quality pharmaceutical operations. This role offers a challenging yet rewarding chance to apply your specialist knowledge and help shape the future of healthcare products.
Key Responsibilities:
- Provide expert guidance on GMP compliance, facility operations, and quality systems within a pharmaceutical manufacturing environment
- Collaborate with laboratory teams to optimize processes, enhance compliance standards, and ensure adherence to regulatory requirements
- Support the organization in rectifying issues identified during FDA inspections and implement robust quality measures
- Lead initiatives to upgrade facility and process controls, ensuring alignment with industry best practices and regulatory expectations
- Work closely with cross-functional teams, sharing your expertise to drive continuous improvement and operational excellence
Required Skills:
- Extensive experience as an SME in GMP, Quality Assurance, or Facility Management within the pharmaceutical or biotech sectors
- Proven track record of supporting GMP compliance, especially in environments transitioning from cosmetic to pharmaceutical manufacturing
- Strong understanding of regulatory standards such as FDA, EMA, and other relevant authorities
- Ability to analyze complex processes and implement practical, compliant solutions
- Excellent communication skills in English; fluency in Swedish is highly desirable but not mandatory
Nice to Have Skills:
- Experience working with cosmetic and pharmaceutical product manufacturing
- Previous involvement in FDA inspections and compliance remediation
- Project management capabilities and leadership experience in a GMP environment
- Knowledge of laboratory quality systems and process optimization
Preferred Education and Experience:
- Bachelor’s or higher degree in Life Sciences, Pharmacy, Chemistry, or related fields
- Senior-level expertise, with a minimum of 10+ years in quality assurance, GMP, or facility management roles
- Demonstrated success in advisory or consultation roles within regulated manufacturing environments
Other Requirements:
- Fully onsite position in Uppsala with minimal home working
- Ability to start immediately or within a short notice period
- Willingness to travel as needed within the region
Seize this opportunity to influence a major client’s regulatory compliance and help advance critical pharmaceutical manufacturing processes. Apply now with your updated CV and cover sheet–make your expertise count and be a key player in a transformative project!
Equal Opportunity Employer
We are proud to be an equal opportunity employer. We welcome and encourage applications from all qualified candidates regardless of race, sex, gender identity or expression, disability, age, religion or belief, sexual orientation, or any other characteristic protected by applicable laws and regulations. It is our policy not to discriminate against any applicant or employee, and we are committed to fostering a diverse, inclusive, and respectful work environment across all locations in which we operate. We believe that diversity, equity, and inclusion are fundamental to our mission and enhance our ability to serve clients globally. If you have a disability or require any reasonable accommodations during the application or interview process, please inform your recruiter or contact us directly so that we can explore the appropriate arrangements.
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