Labeling and Artwork Associate

Posted 3 Hours Ago
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Walton, Cumbria, England, GBR
Hybrid
Entry level
Artificial Intelligence • Healthtech • Machine Learning • Natural Language Processing • Biotech • Pharmaceutical
We’re in relentless pursuit of breakthroughs that change patients’ lives.
The Role
Supports compliant publication of approved SPCs and PILs across UK, Ireland, and other markets. Manages labeling requests, document uploads, portal workflows, publication checks, audit trails, system data integrity, and issue resolution. Provides administrative and operational support to Labeling Managers while ensuring accurate, timely, inspection-ready records and compliance with procedures.
Summary Generated by Built In
Job Summary
The Labeling Associate supports the compliant and timely publication of product information, and ensures SPCs and PILs are accurately prepared and supported with complete, inspection-ready documentation. Working closely with Labeling Managers and other stakeholders, the role maintains labeling systems, workflow tools and mailboxes, and also supports regional labeling and artwork activities according to business needs.
Job Responsibilities
  • Manage labelling publication: process approved SPCs and PILs for countries including UK and Ireland, monitor incoming requests, confirm that required documents and supporting information are complete. Support publication or associated labelling activities for markets where required.
  • Prepare and publish approved documents accurately: complete administrative formatting , upload documents to the correct portal completing associated actions.
  • Complete publication checks and follow-up: monitor portal notifications, quality-control comments, approvals, and publication status, and verify that the correct document and version available.
  • Maintain compliance records and tracking: keep a complete, accurate, and inspection-ready audit trail; work in accordance with approved procedures, Job Aids, and portal guidance; meet established timelines.
  • Identify, resolve issues: identify incomplete or inconsistent requests, obtain missing information, support independent quality checks and resolve portal issues.
  • Provide operational and administrative support to Labeling Managers where appropriate.
  • Support Labeling Manager by maintaining system management for labeling activities.
  • Monitors system data integrity and quality checks .

Here Is What You Need:
  • Degree in life sciences, pharmacy, or a related field or equivalent professional experience
  • Hands-on experience related to development, maintenance and commercialization activities
  • Demonstrated ability to build strong, positive working relationships across multiple cultures and locations.
  • Strong administrative, document-management or operational skills, with demonstrated accuracy when handling detailed information.
  • Good written and verbal English and competence using Microsoft Office applications.
  • Ability to work independently, while recognizing when guidance or escalation is required.
  • Ability to work under tight timelines, apply sound judgment.

Bonus Points If You Have:
  • Experience in a pharmaceutical, healthcare, regulatory or other highly regulated environment.
  • Experience in labeling, artwork, regulatory affairs, publishing, document management, quality/compliance, controlled records or audit trails.
  • Familiarity with SPCs, PILs, product information or international team working.
  • Preferred experience with business analytics tools
  • Proven technical aptitude and the ability to quickly learn new software, regulations, and standards.
  • Ability to speak additional European language.

Work Location Assignment: Hybrid (some office presence is required)
Purpose
Breakthroughs that change patients' lives... At Pfizer we are a patient centric company, guided by our four values: courage, joy, equity and excellence. Our breakthrough culture lends itself to our dedication to transforming millions of lives.
Digital Transformation Strategy
One bold way we are achieving our purpose is through our company wide digital transformation strategy. We are leading the way in adopting new data, modelling and automated solutions to further digitize and accelerate drug discovery and development with the aim of enhancing health outcomes and the patient experience.
Flexibility
We aim to create a trusting, flexible workplace culture which encourages employees to achieve work life harmony, attracts talent and enables everyone to be their best working self. Let's start the conversation!
Equal Employment Opportunity
We believe that a diverse and inclusive workforce is crucial to building a successful business. As an employer, Pfizer is committed to celebrating this, in all its forms - allowing for us to be as diverse as the patients and communities we serve. Together, we continue to build a culture that encourages, supports and empowers our employees.
DisAbility Confident
We are proud to be a Disability Confident Employer and we encourage you to put your best self forward with the knowledge and trust that we will make any reasonable adjustments necessary to support your application and future career. Our mission is unleashing the power of our people, especially those with unique superpowers. Your journey with Pfizer starts here!
To learn more about acceptable and prohibited uses of AI during the recruitment process, please review our candidate AI-use guidelines available on Pfizer Careers .
Regulatory Affairs
#BI-Hybrid

Skills Required

  • Degree in life sciences, pharmacy, or a related field, or equivalent professional experience
  • Hands-on experience related to development, maintenance, and commercialization activities
  • Ability to build strong working relationships across multiple cultures and locations
  • Strong administrative, document-management, or operational skills with accuracy handling detailed information
  • Good written and verbal English
  • Competence using Microsoft Office applications
  • Ability to work independently and recognize when guidance or escalation is required
  • Ability to work under tight timelines and apply sound judgment
  • Experience in a pharmaceutical, healthcare, regulatory, or highly regulated environment
  • Experience in labeling, artwork, regulatory affairs, publishing, document management, quality or compliance, controlled records, or audit trails
  • Familiarity with SPCs, PILs, product information, or international team working
  • Experience with business analytics tools
  • Technical aptitude and ability to learn new software, regulations, and standards quickly
  • Ability to speak an additional European language

What the Team is Saying

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The Company
HQ: New York, NY
121,990 Employees
Year Founded: 1848

What We Do

Our purpose ensures that patients remain at the center of all we do. We live our purpose by sourcing the best science in the world; partnering with others in the healthcare system to improve access to our medicines; using digital technologies to enhance our drug discovery and development, as well as patient outcomes; and leading the conversation to advocate for pro-innovation/pro-patient policies.

Why Work With Us

We are the inventors, the problem solvers, the big thinkers — those who surmount any hurdle to deliver breakthrough medicines to the people who are counting on them the most.

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Employees engage in a combination of remote and on-site work.

Typical time on-site: 2.5 days a week
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