Freelance/Contract - GMP Facility Management Consultant

Location: Sweden; mainly onsite just north of Solna, with office-based work in Uppsala

Company

hirify.global provides consulting and advisory solutions across regulatory sciences, clinical research, quality and compliance, pharmacovigilance, medical information, and R&D technology for biotech, medical device, and pharmaceutical organizations.

What you will do

• Evaluate current GMP facility activities and identify improvement opportunities.
• Lead GMP facility improvement activities and support inspection readiness.
• Review and update SOPs, work instructions, and related documentation.
• Provide technical support for GMP-critical system activities.
• Assess regulatory compliance with department heads and implement corrective changes.
• Act as the subject matter expert and support ongoing client projects through completion.

Requirements

• BSc degree or higher in a life-sciences discipline.
• Extensive experience in the pharmaceutical or biotechnology sector.
• Extensive SME-level experience in GMP facility management.
• Strong problem-solving skills and experience supporting corrective procedures and regulatory compliance.
• Fluent English is required; Swedish is desirable.
• Ability to work mainly office-based in Uppsala and onsite near Solna throughout the project.

Nice to have

• Experience managing complex GMP facility issues and developing solutions.
• Thorough knowledge of FDA regulations.

Culture & Benefits

• Full-time hours at 1.0 FTE for a project lasting at least four months.
• Immediate-start interim or contract project supporting a leading global life-sciences group.
• Independent consultants are preferred.
• Inclusive workplace focused on diversity, equity, inclusion, collaboration, and innovation.
• Some remote working is supported, although in-person collaboration is encouraged where practical.

Hiring process

• Applications are personally reviewed by the recruitment team.
• Applicants receive an outcome after the application review.