Labeling and Artwork Associate

Biopharma Asia

Reigate and Banstead

Hybrid

GBP 35,000 - 55,000

Full time

4 days ago
Be an early applicant

Get a reply from this employer

Your resume and cover letter, tailored to exactly what they’re hiring for.

Get past ATS filters

Job summary

Pfizer is seeking a Labeling Associate to support compliant and timely publication of product information. You will prepare SPCs and PILs, maintain labeling systems and workflows, and collaborate with labeling managers across regions to ensure inspection-ready documentation.

The role requires a life sciences degree or equivalent experience, strong English communication, and the ability to work under tight timelines in a hybrid work setting.

Qualifications

  • Degree in life sciences, pharmacy, or related field or equivalent experience.
  • Strong written and verbal English communication.
  • Good administrative, document-management or operational skills.

Responsibilities

  • Manage labelling publication: process SPCs and PILs for UK/IRL, ensure documents are complete.
  • Prepare and publish approved documents, complete formatting and portal uploads.
  • Perform publication checks and follow-ups; verify correct document/version.
  • Maintain audit trails and compliance records per procedures and guidance.
  • Support labeling managers and maintain labeling systems and workflows.
  • Monitor data integrity and assist in labeling activities across regions.

Skills

Life sciences
English communication
MS Office proficiency

Education

Life sciences / Pharmacy degree

Tools

Microsoft Office

Job description

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 apatient 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 iscommitted to celebratingthis,in all itsforms – 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
Get your free, confidential resume review.

or drag and drop your file here.

Similar jobs

Similar jobs worth comparing

Labeling and Artwork Associate
Labeling and Artwork Associate

Pfizer • United Kingdom

Hybrid
GBP 30,000 - 42,000
Labeling and Artwork Associate
Labeling and Artwork Associate

5Y9 Pfizer R&D UK Limited • Reigate and Banstead

Hybrid
GBP 30,000 - 45,000
Europe Regulatory Strategist
Europe Regulatory Strategist

5Y9 Pfizer R&D UK Limited • Reigate and Banstead

Hybrid
GBP 85,000 - 120,000
Europe Regulatory Strategist
Europe Regulatory Strategist

Pfizer • Tadworth

Hybrid
GBP 85,000 - 112,000
Europe Regulatory Strategist
Europe Regulatory Strategist

Pfizer • United Kingdom

Hybrid
GBP 65,000 - 95,000
Director, Product Lead
Director, Product Lead

Pfizer • Reigate and Banstead

Hybrid
GBP 90,000 - 120,000
Operations And Key Initiatives Lead
Operations And Key Initiatives Lead

Pfizer • England

Hybrid
GBP 120,000 - 180,000
Director, Product Lead
Director, Product Lead

Pfizer • Stone Cross

Hybrid
GBP 90,000 - 130,000
Director, Product Owner
Director, Product Owner

Pfizer • England

Hybrid
GBP 90,000 - 130,000
Hybrid work model
Undergraduate Regulatory Strategist
Undergraduate Regulatory Strategist

Pfizer • Reigate and Banstead

Hybrid
GBP 18,000 - 24,000
Flexible working arrangements
Professional membership for TOPRA
Shadowing opportunities