QA Officer

EPM Scientific; Tessenderlo; Hybride; EUR 59 000 - 72 000; Plein temps

Avantages offerts par ce poste

Hybrid work arrangement

Career progression opportunities

Résumé du poste

EPM Scientific in Tessenderlo, Belgium, is seeking a Quality Assurance professional to maintain and improve the site's quality systems, ensuring regulatory compliance and driving continuous improvement.

You will coordinate CAPAs, audits, non-conformities, and document control across functions, with hybrid on-site two days per week, and a clear progression path in a growing life sciences company.

Qualifications

• Quality Assurance experience within Medical Devices or a regulated life sciences environment.
• Knowledge of Quality Management Systems (QMS).
• Experience managing CAPAs, non-conformities, investigations, and document control activities.
• Experience supporting audits and compliance activities.
• Fluent English required; additional European languages are advantageous.

Responsabilités

• Manage quality documentation and document control processes.
• Support the maintenance and continuous improvement of the Quality Management System (QMS).
• Lead and coordinate CAPA activities and follow-up actions.
• Support internal and external audits.
• Investigate and manage non-conformities and quality events.
• Ensure compliance with quality standards, regulatory requirements, and internal procedures.
• Collaborate with cross-functional teams to drive quality improvements.
• Support quality and compliance initiatives across the organisation.

Connaissances

Quality Assurance

QMS knowledge

CAPA management

Audits support

Documentation control

Description du poste

Location: Tessenderlo-Ham, Belgium (Hybrid, 2 days per week on-site)
Salary: Up to €65,000 + Benefits

Are you looking for a Quality Assurance role that offers genuine career progression rather than just more of the same?

Do you want to join a growing life sciences company where you'll broaden your skillset, gain greater responsibility, and contribute to a business on an exciting growth trajectory?

On offer is the opportunity to join an international life sciences organisation at a particularly exciting stage of its growth journey. With continued investment across the business, increasing demand for its products, and expansion of its European operations, this is an excellent time to become part of the team.

You'll gain exposure to a broad range of Quality Assurance activities, develop expertise across multiple areas of quality management, and work within a business that actively supports professional development and internal progression.

This company is a highly respected organisation operating within the life sciences sector, supplying innovative products and technologies that support critical applications across pharmaceuticals, biotechnology, diagnostics, and laboratory environments.

The business is experiencing sustained growth in both revenue and headcount, creating new opportunities for employees to advance their careers while contributing to the success of a company operating in a growing and resilient industry.

In this role, you will play a key role in maintaining and improving the site's quality systems, ensuring compliance with relevant standards and regulatory requirements.

You will work closely with colleagues across the organisation to manage quality documentation, coordinate CAPAs, support audits, investigate non-conformities, and help drive continuous improvement initiatives throughout the business.

The ideal candidate will have previous Quality Assurance experience within Medical Devices or another regulated life sciences environment such as pharmaceuticals, biotechnology, diagnostics, laboratory equipment, healthcare products, or related industries.

You'll be someone who enjoys working in a collaborative environment, takes ownership of quality activities, and is looking to continue developing their career within a growing organisation.

This role is ideal for a QA professional seeking a role that offers long-term progression, broader responsibility, and the opportunity to expand their quality expertise within a business that is investing heavily in its future.

The Role

• Manage quality documentation and document control processes
• Support the maintenance and continuous improvement of the Quality Management System (QMS)
• Lead and coordinate CAPA activities and follow-up actions
• Support internal and external audits
• Investigate and manage non-conformities and quality events
• Ensure compliance with quality standards, regulatory requirements, and internal procedures
• Collaborate with cross-functional teams to drive quality improvements
• Support quality and compliance initiatives across the organisation

Who We're Looking For

• Quality Assurance experience within Medical Devices or a regulated life sciences environment
• Knowledge of Quality Management Systems (QMS)
• Experience managing CAPAs, non-conformities, investigations, and document control activities
• Experience supporting audits and compliance activities
• Strong organisational and communication skills
• Ability to work effectively with stakeholders across different functions
• Fluent English required; additional European languages are advantageous

What's On Offer

• Salary up to €65,000
• Hybrid working arrangement (2 days per week on-site)
• Clear progression opportunities as the business continues to grow
• Opportunity to build valuable experience across quality systems, compliance, investigations, and auditing
• Join a company experiencing significant growth in both revenue and headcount in the growing life sciences industry

Long-term career development opportunities within an international organisation