Join a groundbreaking leader in pharmaceutical biotechnology, dedicated to developing life-changing medicines. In this role, you'll meticulously review and ensure the quality of artworks, including labels and leaflets, produced by the company and its partners. Your keen eye for detail and commitment to maintaining high standards will contribute to process improvements within a regulated environment. Collaborate with internal teams, optimize artwork processes, and ensure compliance with regulatory requirements. Continue reading to see how we can support your professional growth.

Over het bedrijf

SIRE Life Sciences

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The company
Our client is a groundbreaking leader in pharmaceutical biotechnology, with over 40 years of pioneering advancements in developing life-changing medicines to improve the lives of patients worldwide
The role
In this role, you will be responsible for carefully reviewing artworks produced by our client and its partner, including print proofs from suppliers. You will assess both manually and automatically generated artworks, ensuring they meet their quality standards and regulatory requirements. If you are committed to maintaining high-quality standards and are eager to contribute to process improvements within a regulated environment, we encourage you to apply.
Responsibilities

Review artworks, including labels, leaflets, and production materials, created by the clients and its partner clients, ensuring compliance with GMP standards.
Conduct thorough reviews of artworks in accordance with the companies Standard Operating Procedures.
Contribute to optimizing artwork processes and support continuous improvements in quality and efficiency.
Work closely with internal teams to resolve artwork-related issues and ensure a seamless production workflow.
Participate actively in team meetings and provide valuable feedback on artwork processes.
Review artworks from both manual and automated creation sources to ensure consistency and compliance.
Ensure all designs meet regulatory standards and compliance requirements, maintaining meticulous attention to detail in all reviews.

Requirements

Bachelor’s degree in Graphic Arts, Packaging, Life Sciences, or a related field.
2+ years of Packaging/Labeling experience focused on artwork creation in a GMP environment.
2+ years of relevant work experience in a highly regulated industry, particularly the pharmaceutical industry.
Experience with pharmaceutical labeling regulations and standards.
Proven track record of collaborating with cross-functional teams to achieve common objectives.
Self-motivated, proactive, and adaptable to change.
Experience with Microsoft Office (Excel, Word, PowerPoint) and visual tools (e.g., Tableau, PowerBI).

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