Looking for Quality Assurance jobs in Europe? ProPharma is hiring a Quality Assurance Consultant for a permanent full-time position in Sweden. This is an excellent opportunity for professionals with GxP compliance and regulatory experience to join a global leader in pharmaceutical consulting. Apply now for this ProPharma Sweden role.
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About the Company
ProPharma has been improving patient health and wellness for over 20 years by providing expert advice and solutions to biotech, medical device, and pharmaceutical companies worldwide.
The company operates through an advise-build-operate model across the entire product lifecycle. With deep expertise in regulatory sciences, clinical research, quality & compliance, pharmacovigilance, and R&D technology, ProPharma delivers fully customizable consulting services that help clients de-risk and accelerate their drug and device programs.
Job Details
- Company Name: ProPharma
- Job Title: Quality Assurance Consultant
- Job Requisition ID: JR 9267
- Location: Sweden
- Job Type: Permanent, Full-time
- Experience: Minimum 2 years in quality assurance and GxP compliance
- Qualification: Bachelor’s degree in a scientific discipline
- Work Type: Hybrid (office + remote, as agreed with manager)
Job Description
ProPharma is seeking a Quality Assurance Consultant to support clients in managing product quality complaints, GxP requests, and quality systems. The role involves providing expert consultation on deviations, non-conformances, CAPA implementation, and ensuring compliance with EMA and MHRA regulations.
This position plays a key role in implementing risk-based and phase-appropriate GxP projects while promoting continuous improvement in quality and customer satisfaction.
Essential Functions
- Manage product quality complaints for clients
- Support clients with various GxP requests
- Represent ProPharma in assigned quality assurance areas
- Contribute to the implementation and execution of risk-based GxP projects
- Provide consultation on deviations, non-conformances, and CAPA implementation
- Support development of quality systems through SOP writing and training
- Educate employees on compliance and quality assurance
- Promote continual improvement in customer satisfaction
Skills/Qualifications
- Strong knowledge of EMA and MHRA regulations and guidance documents
- Expertise in GxP systems and quality assurance consulting
- Minimum 2 years of relevant experience in QA and GxP compliance
- Bachelor’s degree in a scientific discipline
- Excellent written and oral communication skills in English (additional European language preferred)
- Strong interpersonal skills and ability to build client confidence
- High attention to detail and quality orientation
- Strong analytical and problem-solving skills
- Ability to manage multiple tasks simultaneously
- Willingness to travel as required
- Finnish language skills are highly desirable
Key Responsibilities
- Handle product quality complaints and GxP-related queries
- Provide expert consultation on quality and compliance issues
- Implement proper CAPA to resolve deviations and non-conformances
- Develop and improve quality management systems (QMS)
- Write SOPs and deliver training on quality principles
- Ensure compliance of operations with regulatory requirements
- Engage with clients and internal teams to drive continuous improvement
Benefits/Perks
- Permanent full-time position with a global consulting leader
- Opportunity to work on high-profile drug and device programs
- Hybrid work model with flexibility
- Strong focus on diversity, equity, and inclusion
- Career growth and professional development opportunities
- Collaborative and innovative work environment
- Safe space to unleash entrepreneurial spirit
How to Apply
All applications to roles at ProPharma are personally reviewed by the recruitment team. Apply directly for Job Requisition ID: JR 9267 through the official ProPharma career portal.
Verified Post
Verification: To confirm the legitimacy of this posting, you can view the original announcement on the ProPharma Career page.
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Note: ProPharma does not accept unsolicited resumes from recruiters or third parties.
For more QA jobs, GxP jobs, pharma consulting jobs, and regulatory opportunities in Europe and India, visit Pharma Recruiter.
Why You Should Join ProPharma
ProPharma offers a unique opportunity to work with cutting-edge biotech and pharmaceutical clients while contributing to therapies that improve patient lives. With a strong emphasis on innovation, collaboration, and continuous improvement, the company provides a supportive environment where professionals can grow their expertise in quality assurance and regulatory compliance on a global scale.
FAQs
What is the minimum experience required for the Quality Assurance Consultant role at ProPharma?
A minimum of 2 years of relevant experience in quality assurance and GxP compliance is required.
What qualifications are needed for this position?
Candidates must hold a Bachelor’s degree (or equivalent) in a scientific discipline.
Is Finnish language mandatory for the Sweden QA job?
Finnish language skills are highly desirable but not mandatory. Strong English communication is essential.
What is the work arrangement for this role?
The position follows a hybrid model. New hires are encouraged to spend some time in the office as agreed with the manager.
Does this role require travel?
Yes, willingness and ability to travel as required is part of the role.
