Senior QA & Compliance Officer

Location: Netherlands

SIRE® is the market leader in Life Sciences recruitment. We believe the recruitment market needs to gear up in technology and continuous innovation. We like technology, in a Life Sciences market driven on science, we couldn’t stay behind; we drive Recruitment Science. Investing a majority of our turnover in technology enables us to use unique Resource Technologies. By using highly advanced algorithms, we enable our team of Resource & Data Strategists© to maintain the most advanced, detailed and complete Life Sciences network in Europe. This big data enables us to work Reverse Recruitment©: we first analyze the market in-depth before we go out to the market. Because we analyze the whole market, we can compare facts and data. This enables us to do Facts & Big Data Recruitment©, making sure we, or better yet, you find the right career!Our client is a professional Pharmaceutical organisation, based in Noord-Brabant Netherlands.

The Company

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Role Description

The QA Operations & Compliance officer needs to ensure distribution-and product finishing processes are compliant with AQ and AN-policies as well as all applicable regulations and legislations.

Responsibilities

Internal/Supplier Auditing - Responsible for performing and follow up of the internal/supplier audit program.
External Auditing - Supports auditors in the effective and efficient execution and documentation, investigation, impact assessment, and CAPA planning.
Participates actively in projects that involve QA.
Supports the doc control process including the creation of QA related procedures.
Continuously evaluates the performance of the assigned quality system and initiates and implements improvement initiatives.
Exception Management - Leads and participates in the exception management process.
Contributes to the development and maintenance of the quality policies and systems to ensure business objectives can be achieved.
Participates in Food Safety Team.
Participates in validation projects; advises regarding classification and requirements for the performance of the validation of the systems/equipment.
Supports QA related Product Finishing - and warehouse activities in line with procedures and GMP food/FDA and HACCP standards.
Supports complaint handling processes.
Reviews and authorizes validation protocols and reports. Is responsible for the final release of a system/equipment upon validation. And as such will participate in the Validation Review Board (VRB).
Act as product action officer in weekly duties of 7 calendar days, accessible 24/7.

Requirements

Minimally a 4-year bachelor’s degree is required
Dutch and English language in word and writing.
Combined of 2 to 6 years in one or more positions directly related to manufacturing or distribution operations in the nutritional or pharmaceutical industry.
Experience in working with cross functional /-department (international) projects with demonstrated effective communication, teamwork and problem-solving skills.
Very accurate and a passion for Quality and Supply Chain.
Extensive experience in quality systems and quality assurance in an operational setting with demonstrated knowledge of techniques for assessing the quality of processes and the ability to guide others in these activities.
Experience with IT and equipment validation, HACCP and FSMA.

Are you interested and do want to apply for this role, please fill out your application via the apply button below and contact Seppe Verhoeven.