Artwork Reviewer - Global Artwork
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Career Category
Business Development
Job Description
Job Summary
We are seeking a talented Artwork Reviewer who is willing to grow and develop their career within our team.
As an Artwork Reviewer, you will be responsible for reviewing artworks, both created manually or automatically, for all Amgen products in any stage of development (test, Mock-up, master), as well as reviewing artwork (brand) templates, design templates, supplier print proofs, and artwork generated by Amgen partners.
Key Responsibilities:
Artwork Review in compliance with Amgen’s Standard Operating Procedures: Review artworks, both manually or automatically, for all Amgen products and in different stages of development (test, mock-up, masters).
Review templates: technical layout templates (TLTs), design templates, brand templates
Review Supplier Print Proofs.
Review and approve Artworks created by Amgen partners
Provide input to optimize artwork processes, and support continuous process and quality improvements.
Participate in team meetings.
Basic Qualifications:
Bachelor’s degree in graphic design & 1-2 years of Packaging/Labeling experience in a GMP environment.
Proficiency in graphic design software such as Adobe Creative Suite (Photoshop, Illustrator, InDesign) and other relevant tools.
Solid understanding of design principles withing pharma industry.
Knowledge of print production processes and prepress requirements.
Preferred Qualifications:
Some relevant work experience in a highly regulated industry / cGMP pharmaceutical industry.
Experience with Microsoft Office software (Excel, Word, Power Point), visual tools (e.g. Tableau, PowerBI, Google Charts), and Document Management System (e.g VEEVA vault).
Skills:
Excellent communication skills and the ability to present and articulate design concepts effectively.
Strong attention to detail.
Ability to work independently as well as collaboratively in a fast-paced environment.
Creative thinking and problem-solving skills.
Flexibility to adapt to changing priorities and project requirements.
Demonstrate sound judgement.
Continuous improvement mindset.
Self-motivated individual who demonstrates willingness to learn and be receptive to change.
Great interpersonal and communication skills.
Ability to uphold a sense of personal accountability.
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Job details
How this role compares
Computed from every other active Manufacturing & CMC role in our database, not just this employer's listings.
We currently track 2561 comparable Manufacturing & CMC roles across 172 biopharma companies.
Salary context
675 of 2561 peers report a salary range (USD, annualized)
Peers share this role's job function. This posting doesn't list a seniority level, so peers aren't narrowed by seniority either -- the range below may span more levels than usual.
Where these roles are based
Top locations among the 2561 comparable roles
+ 48 more countries
Seniority mix
1167 of 2561 peers have a known seniority level
Therapeutic area mix
11 of 2561 peers have a known therapeutic area; the rest are genuinely unlabeled, not hidden
Similar opportunities
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How we calculate "similar"
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Every comparison starts from the same 100-point budget: 25 for working in the same function, 40 for the same therapeutic area, 20 for the same or adjacent seniority, 15 for the same country. A dimension we can't confirm on both sides contributes nothing, never a guess, never a free pass.
0 points, never a partial guess. A role we know almost nothing about beyond its function bottoms out at 25%; it never inflates to 100% just because there's little to compare against. Seniority uses a defined ladder (Associate → Manager → Associate Director → Senior → Principal → Director → Senior Director → Executive/VP) so "Director" and "Senior Director" count as adjacent, but "Director" and "Executive/VP" do not.