Manager, Artwork Development QC

As ADVANZ PHARMA continues to strengthen its position as the partner of choice for specialty, hospital, and rare disease medicines, we are seeking a Manager, Artwork Development QC to join our Medical Office team.

The Manager, Artwork Development QC provides end-to-end management of quality, compliance, and timely delivery of artworks of products in the ADVANZ PHARMA portfolio.

The role is a combination of individual contributory components (i.e., expert review of design and regulatory content of artworks assigned) and a team management component (job allocation, planning and workload management, overseeing work done by the Artwork QC team) – both having an equal distribution.

This role may also be required to project-manage cross-functional initiatives and co-ordination with CMO.

The basic essence of this role is to ensure that an artwork accurately reflects approved regulatory information, meets technical requirements, and is released through controlled systems and documented processes.

What You'll Be Responsible For Lead end-to-end artwork quality control for pharmaceutical packaging and product information artwork, ensuring accuracy from initial brief through final approval.

Perform independent verification and detailed content reviews to confirm artwork aligns with approved regulatory documents, technical specifications, safety information, and market-specific requirements.

Conduct design and technical QC covering layout, readability, typography, colours, symbols, barcodes, dimensions, print specifications, component identification, and consistency across packaging components.

Ensure regulatory compliance and traceability by aligning artwork changes with approved dossiers, labelling commitments, change controls, regulatory variations, safety updates, and business requirements.

Manage artwork-related risks and quality records, ensuring deviations, exceptions, risk assessments, decisions, and change controls are properly documented, escalated, and closed.

Oversee multiple concurrent artwork projects and portfolios, managing scope, timelines, dependencies, stakeholders, risks, implementation dates, and workflow completion to meet business deadlines.

Drive project performance and continuous improvement through metrics such as cycle time, right-first-time performance, review turnaround, rework, deviations, and on-time delivery.

Serve as a pharmaceutical artwork and regulatory SME, providing expertise in packaging, labelling, compliance requirements, documentation practices, controlled change management, and implementation of evolving regulations and standards.

Strengthen governance, systems, and process excellence by maintaining SOPs, improving artwork management systems, implementing risk-based QC approaches, identifying automation opportunities, and leading root-cause analysis and preventive actions.

Lead and develop the Artwork QC team and stakeholder relationships, including people management, capability building, performance monitoring, vendor oversight, cross-functional collaboration, audit support, and representation in senior management reviews and inspections.

Thrive in an entrepreneurial environment and take accountability for results.

Embrace challenge and change, applying a growth mindset approach.

Have a bias for action and fast decision-making.

Consistently demonstrate and embody company core values: Entrepreneurship, Speed, and Integrity.

Drive the spirit of “One Team” by working collaboratively across all business functions with open, honest, and respectful cooperation.

Contribute to making ADVANZ PHARMA a desired place to work.

What We're Looking For We're looking for ambitious, resilient, and commercially minded professionals who are passionate about improving patient outcomes and driving business growth.

For this role, you will also have the following: Qualifications: Bachelor’s degree in pharmacy, Pharmaceutical Sciences, Chemistry, Life Sciences, or Packaging Technology.

Project Management certification Knowledge, Skills & Experience: 8–10 years of relevant experience in pharmaceutical/regulatory artwork QC, packaging operations, regulatory labelling, pharmaceutical design production or a closely related regulated environment.

Hands-on experience reviewing both regulated content and visual/technical artwork quality, with evidence of strong error detection and risk-based judgement.