Quality Assurance, CQV and LIMS Specialist Jobs Worldwide

Explore 2025 global job openings in Quality Assurance Consultant, Senior Quality Systems Specialist (CQV), LIMS Support Specialist (Canada & USA), CQV Analyst (Brazil), and QA Junior Support (Spain). Apply today for exciting pharmaceutical and biotech career opportunities with a global leader in quality and compliance.

Global Job Openings – Quality Assurance, CQV, and LIMS Specialist Careers

World’s leading providers of engineering, quality, and regulatory services to the pharmaceutical, biotechnology, and life sciences sectors. As we move into 2025, the company is expanding its global presence with several exciting career opportunities across Finland, Spain, Canada, the United States, and Brazil.

These positions include highly skilled roles such as Quality Assurance Consultant, Senior Quality Systems Specialist (CQV), LIMS Support Specialist, CQV Analyst, and QA Junior Support. Each position plays a critical role in maintaining compliance, advancing pharmaceutical quality systems, and ensuring patient safety through robust processes.

1. Quality Assurance Consultant – Helsinki, Finland

The Quality Assurance Consultant in Helsinki will play an essential role in ensuring regulatory compliance and maintaining the Quality Management System (QMS) for local affiliates.

Key Responsibilities:

• Implement and maintain QMS aligned with company and regulatory standards.
• Manage risk assessments, complaints, deviations, CAPAs, and change control systems.
• Oversee authority inspections, self-inspections, and GxP surveillance.
• Lead product quality reviews (PQR) and training management.
• Supervise GDP requirements, warehousing, and product distribution.

Qualifications:

• Bachelor’s degree in Quality, Life Sciences, or related field.
• Minimum of 5 years of QA experience in the pharma or healthcare industry.
• Strong understanding of GxP, GDP, and global compliance frameworks.

This role is ideal for professionals who excel at regulatory compliance, risk management, and quality leadership in a dynamic, global environment.

Apply for this role

2. Senior Quality Systems Specialist – CQV Expert (Girona, Spain)

Spanish operations are seeking a Senior Quality Systems Specialist with strong CQV (Commissioning, Qualification, and Validation) experience.

Responsibilities include:

• Oversee equipment, facility, and process qualification (IQ/OQ/PQ).
• Conduct risk assessments, CAPA implementation, and root cause analysis.
• Support inspections and maintain high readiness for regulatory audits.
• Mentor junior staff in validation procedures and quality systems.
• Collaborate with cross-functional teams to uphold compliance with EMA, FDA, and ICH standards.

Requirements:

• Bachelor’s degree in science or engineering.
• 5+ years of experience in pharmaceutical or biotech quality roles.
• Deep understanding of CQV principles and validation protocols.
• Fluency in English and Spanish.

This position is ideal for professionals passionate about ensuring manufacturing quality through rigorous CQV processes and technical leadership.

Apply here

3. LIMS Support Specialist – Toronto, Canada

As a LIMS Support Specialist (Quality Control), you’ll be responsible for managing LIMS configuration, master data governance, and technical support in alignment with GMP regulations.

Key Responsibilities:

• Configure and customize LIMS platforms (LabWare, STARLIMS, etc.) for QC workflows.
• Build master data governance models ensuring data integrity and regulatory alignment.
• Serve as the LIMS System Owner, managing upgrades and system changes.
• Collaborate with IT and QC teams globally for analytical data management.

Qualifications:

• Experience in LIMS systems within GMP-regulated labs.
• Strong grasp of QC workflows, analytical testing, and compliance.
• Excellent communication, documentation, and coordination skills.
• Eligibility to work in Canada and the U.S.

This position is perfect for professionals combining technical IT expertise with pharmaceutical quality control knowledge.

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4. LIMS Support Specialist – Swiftwater, Pennsylvania, USA

A similar LIMS Support Specialist role is available in Swiftwater, PA, offering either a consulting or full-time position.

Responsibilities:

• Manage LIMS configurations and upgrades for QC operations.
• Support audit readiness, system validation, and data integrity compliance.
• Lead LIMS data governance projects and master data documentation.
• Work cross-functionally with IT and QC teams to enhance lab efficiency.

Requirements:

• Proficiency with LIMS software in GMP-regulated environments.
• Strong technical and analytical capabilities.
• Understanding of cGMP and U.S. regulatory expectations.

This U.S.-based role offers a great opportunity for professionals passionate about quality systems digitalization and lab automation in regulated environments.

Apply here

5. CQV Analyst – São Paulo, Brazil

Expanding its footprint in Latin America with a CQV Analyst position in São Paulo, Brazil.

Key Responsibilities:

• Develop and execute commissioning, qualification, and validation protocols for equipment and processes.
• Conduct risk assessments, audits, and identify improvement areas.
• Review and approve validation documentation, deviations, and reports.
• Collaborate with cross-functional teams to ensure compliance.
• Maintain up-to-date knowledge of FDA, ANVISA, and cGMP regulations.

Requirements:

• Bachelor’s degree in Engineering, Pharmacy, or Chemistry.
• At least 3 years of CQV experience in the pharmaceutical sector.
• Proficiency in IQ/OQ/PQ, cleaning validation, and process validation.
• Fluency in English and Portuguese.

This is an outstanding opportunity for professionals looking to grow their careers in a global CQV environment with a focus on compliance excellence.

Apply now

6. QA Junior Support – Madrid, Spain

Hiring a QA Junior Support professional in Madrid, Spain—an excellent entry-level opportunity in the pharmaceutical quality field.

Key Responsibilities:

• Assist with SOP preparation, review, and documentation management.
• Participate in internal/external audits and support CAPA implementation.
• Conduct quality checks to ensure compliance with GMP and company policies.
• Collaborate with cross-functional teams to ensure timely completion of quality projects.
• Maintain and update QA databases and systems.

Requirements:

• Bachelor’s degree in a science-related field.
• 1–2 years of QA experience, preferably in the pharmaceutical sector.
• Familiarity with FDA and GMP guidelines.
• Excellent organizational, communication, and teamwork skills.

This role is ideal for recent graduates or early-career professionals who want to launch a rewarding QA career in a multinational pharmaceutical environment.

Apply here

• Global Reach: Offices and clients across North America, Europe, and Latin America.
• Expert Teams: Specialists in CQV, QA, regulatory affairs, and process engineering.
• Innovation: Adoption of digital tools like LIMS, data integrity systems, and AI-driven QMS.
• Career Growth: Continuous learning and international project exposure.

Whether you’re an experienced Quality Assurance Consultant in Finland, a CQV specialist in Spain or Brazil, or a LIMS expert in North America offers diverse global opportunities to build a fulfilling career.

You contribute to advancing the pharmaceutical industry’s commitment to safety, efficacy, and compliance—while enhancing your professional expertise within a world-class organization.

Apply today for the position that matches your experience and take the next step toward a global career in quality and compliance.