QA specialist

vwr; Hillegom; On-site; EUR 42,000 - 64,000; Full time

Job summary

Avantor is expanding its biopharma manufacturing site in Hillegom and is seeking a dedicated Quality Inspector to join the production quality team. You will ensure regulatory and customer requirements are met through product inspections and documentation review across manufacturing, filling and labeling processes.

Responsibilities include GDP and GDP compliance, supporting investigations of events and complaints, and ensuring adherence to GMP and ISO standards.

Qualifications

• Experience in quality inspection and GMP compliance
• Attention to detail and documentation skills
• Ability to work in a biopharma production environment

Responsibilities

• Comply with company policies, procedures, work instructions, and training requirements focusing on customer service, production, and quality.
• Review order requirements, customer documentation requirements, proper filling and assembly requirements, and ensure other technicians follow GMP requirements.
• Verify adherence to policies, procedures, and work instructions.
• Ensure documentation and physical product segregation and containment of non-conforming material identified during the production process.
• Review production documentation for accuracy, completeness, and GDP compliance.
• Assist in correcting order issues and ensure actions that are taken are appropriate.

Job description

The Opportunity:

If you are ready to discover your greatest potential and lift your career to the next level, Avantor's brand new site in Hillegom offers challenging opportunities in a biopharma environment!

Avantor®, a Fortune 500 company, is a leading global provider of mission-critical products and services to customers in the biopharma, healthcare, education & government, and advanced technologies & applied materials industries. One of our greatest strengths comes from having a global infrastructure that is strategically located to support the needs of our customers.

At Avantor, we set science in motion to create a better world. To achieve this mission, we are currently looking for a one-of-a-kind Quality Inspector.

In this role, you will ensure customer and regulatory requirements have been met by inspecting product and review of documentation throughout all aspects of the production process (e.g., manufacturing, filling, and labeling / assembly, etc.). You will also ensure compliance with all applicable standards and regulations (e.g., ISO 9001, ISO 13485, 21 CFR 820, 21 CFR 11, ISO 17025, and EXCiPACT), Good Manufacturing Practices (cGMPs), and Good Documentation Practices (GDPs). You will be responsible for providing Event and Complaint investigation support to other team members.

YOUR RESPONSIBILITIES

• Comply with company policies, procedures, work instructions, and training requirements focusing on customer service, production, and quality.
• Keep customer interests and regulatory requirements in mind, ensure customer needs are met by reviewing order requirements, customer documentation requirements, proper filling and assembly requirements, and, where needed, ensure other technicians understand and follow documented VWR Solon procedures and GMP requirements. Ensure customer requirements are met.
• Verify adherence to policies, procedures, and work instructions.
• Ensure documentation and physical product segregation and containment of non-conforming material identified during the production process.
• Review production documentation for accuracy, completeness, and GDP compliance.
• Assist in correcting order issues and ensure actions that are taken are appropriate.