SME, STERILITY EXPERT – UPPSALA, SWEDEN

SME, Sterility Expert – Uppsala, Sweden

Location: Uppsala, Uppsala län

Category: Quality and Compliance

Salary: Apply for details

Country: Sweden

Employment: Contract

Worksite: On-Site

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Job Description

Join Our Team as a Sterility Expert (SME) in Uppsala, Sweden – Lead the Transition to Pharmaceutical Excellence

Are you a seasoned expert in sterilisation and quality assurance with a passion for advancing pharmaceutical manufacturing? We are seeking a highly skilled SME, Sterility Expert to play a pivotal role in supporting a leading cosmetic manufacturer’s transition into pharmaceutical production. This on-site opportunity in Uppsala offers a dynamic environment where your expertise will directly impact compliance, process improvements, and operational excellence during a critical phase of transformation.

In this role, you will collaborate closely with laboratory teams and quality professionals to optimise sterilisation processes, enhance GMP adherence, and ensure regulatory compliance following recent FDA inspection setbacks. Your expertise will help shape the future of this company’s pharmaceutical journey, making a tangible difference in product quality and safety.

Key Skills & Qualifications

Extensive experience in sterilisation, sterilisation processes, and related quality assurance within GMP environmentsStrong knowledge of pharmaceutical manufacturing standards and regulatory complianceProven expertise in process improvement and laboratory operationsFamiliarity with GMP regulations and quality control proceduresExcellent problem-solving and communication skills in a fast-paced setting

Fluency in Swedish and English (though English language proficiency is essential)Experience supporting companies through regulatory inspections and transitionsBackground in the cosmetic or pharmaceutical industry

Preferred Education & Experience

Bachelor’s degree or higher in Life Sciences, Pharmacy, Biotechnology, or a related fieldDemonstrated senior-level experience (Senior Manager or above) in sterilisation, quality assurance, or GMP compliancePrevious involvement in transitioning processes from cosmetic to pharmaceutical manufacturing is advantageous

Other Requirements

Fully on-site role in Uppsala – minimal remote workingContract duration of 4 months with a likely extensionAbility to start as soon as possibleCapacity to support the project at a senior expert level, with a focus on delivering immediate impact

This is a unique opportunity to contribute your high-level expertise to a transformative project with a global impact. If you are ready to leverage your sterile processing knowledge and lead a critical quality assurance initiative, we encourage you to apply now. Seize this chance to make a significant difference!

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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