Quality Manager

LIGHTHOUSE Instruments; Diemen; Hybrid; EUR 65,000 - 85,000; Full time

Job summary

LIGHTHOUSE Instruments is seeking a Quality Manager to maintain and continuously improve the Quality Management System in a GMP/non-GMP laboratory. You will ensure compliance with regulations and standards while supporting daily quality activities.

The role requires experience in GMP, risk management, audits, and training, with a focus on fostering a quality-driven culture and cross-functional collaboration. Hybrid work is possible in Diemen area.

Qualifications

• Bachelor-level science degree required (Life Sciences, Chemistry or related).
• 2–5 years of GMP experience in a laboratory environment preferred.
• Strong written and verbal English; Dutch a plus.

Responsibilities

• Maintain, monitor, and improve the QMS in GMP and non-GMP lab settings.
• Lead GMP training and ensure regulatory compliance across the organization.
• Oversee document management: SOPs, policies, and quality records.
• Lead Quality Risk Management activities; perform risk assessments.
• Manage supplier qualification and performance monitoring.
• Coordinate internal audits and support customer/regulatory audits.
• Drive CAPAs and nonconformances; track training and closure of actions.
• Act as primary QA point of contact for quality-related inquiries from customers.

Skills

Quality management

GMP experience

Risk management

Audits and CAPAs

Documentation control

Cross-functional collaboration

SOP development

Regulatory compliance

Education

BSc in Life Sciences/Chemistry or related

Tools

Microsoft Office

QMS software

Job description

As Quality Manager, you will play a key role in maintaining, overseeing, and continuously improving the Quality Management System (QMS) within a GMP-regulated and non-GMP laboratory environment.

In this hands‑on position, you will ensure compliance with applicable regulations, industry standards, and internal quality requirements while actively supporting daily quality activities.

As Lighthouse operates in both GMP and non‑GMP environments, a strong understanding of risk management and a broad perspective on quality and compliance are essential.

You will be responsible for assessing risks, providing compliance guidance across the organization, and ensuring that quality principles are applied appropriately to diverse activities.

Your responsibilities include managing audits, change controls, nonconformances, CAPAs, and training processes, while driving continuous improvement and fostering a quality‑focused culture throughout the business.

Key responsibilities:

• Ensure the maintenance, continuous improvement, and compliance of the Quality Management System (QMS).
• Manage GMP training activities, including the development, delivery, and coordination of initial and ongoing GMP training programs for QA personnel and company employees to ensure compliance with operational requirements.
• Manage the quality documentation system, ensuring regulatory compliance and availability of current and approved documentation. Responsibilities include:
  • Coordinating the creation, review, revision, and approval of quality system documents;
  • Ensuring document validity and lifecycle management;
  • Reviewing and approving Quality Policies and Standard Operating Procedures (SOPs).
• Lead Quality Risk Management activities by facilitating risk assessments and ensuring appropriate quality involvement in business processes based on risk level and regulatory
• Manage supplier qualification and oversight activities, including:
  • Qualification, evaluation, and monitoring of suppliers;
  • Maintenance of the Approved Supplier List.
• Manage audit- and inspection activities, including:
  • Planning and execution of internal audit according to the annual audit plan;
  • Acting as Quality representative during customer audits and regulatory inspections;
  • Supporting both front-office and back-office audit activities.
• Manage the QMS processes by monitoring effectiveness, evaluating proposed quality records, ensuring appropriate impact assessments, and approval in accordance with QMS requirements.
• Act as primary Quality contact for customers regarding quality system‑related requests and requirements:
  • Manage, review, and finalize Quality Agreements with customers;
  • Ensure agreements remain current and compliant;
  • Ensuring timely completion and review of customer quality questionnaires.
• Provide leadership, mentoring, and coaching to QA team members and contribute as a member of the management team.
• Maintain and oversee computerized systems compliance, including:
• Oversee equipment qualification activities, including review and approval of IQ/OQ/PQ protocols and qualification reports.

Qualifications / Requirements:

• BSc degree in Life Sciences/Chemistry/related fields;
• Experience with Microsoft Office and Quality Management systems;
• 2 – 5 years of relevant GMP experience preferably in laboratory environment;
• Strong ability to adapt in dynamic environments;
• Strong self‑reliance skills with the ability to work independently;
• Ability to work effectively with multicultural colleagues and -customers;
• Flexible personality: adapt to unexpected and urgent requests;
• Very well organized and able to set priorities with acute attention to detail;
• Strong written and verbal communication and presentation skills in English, proficiency in Dutch is a plus;
• You reside in or near Diemen and have a valid ‘BSN’

Working hours

The position is for 32 – 40 hours per week during office hours. Hybrid work is possible in consultation.