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Global Pack Design Specialist

GlaxoSmithKline
United States, Pennsylvania, Collegeville
1250 South Collegeville Road (Show on map)
Mar 28, 2025
Site Name: USA - Pennsylvania - Upper Providence
Posted Date: Mar 27 2025

Are you looking to enhance your technical capability by working in a GMP manufacturing environment that allows you to leverage best in class systems and technologies? If so, this Global Pack Design Specialist role could be an ideal opportunity to explore.

As a Global Pack Design Specialist, you will be responsible for the timely creation, approval and delivery of GMP compliant clinical supply labels.

This role will provide YOU the opportunity to lead key activities to progress YOUR career. These responsibilities include some of the following:

  • Work within a global team, create master label content according to existing processes and procedures
  • Perform quality critical checks of label in content produced in various languages within the required timelines
  • Perform quality critical checks of externally produced vendor label proofs prior to receipt by GSK.
  • Creation of label documentation, required for in-country regulatory submissions, in a timely manner.
  • Perform translation management role, working with third party companies to send and receive translations
  • Highlight and root cause label quality issues
  • Own and implement corrective and preventive actions (CAPAs)
  • Creation and sourcing of secondary packaging components
  • Work with external vendors (translation service provider, component suppliers etc)
  • Participate in GPM team meetings
  • Liaise with other groups within Clinical Supply Chain and Quality Assurance

Why you?

Basic Qualifications:

We are looking for professionals with these required skills to achieve our goals:

  • 2 years of experience in (Clinical Good Manufacturing Practices) cGMP environment
  • Experience in a compliance role

Preferred Qualifications:

If you have the following characteristics, it would be a plus:

  • Bachelor's degree preferred.
  • Experience creating and approving master labels.
  • Good knowledge of Clinical Supply requirements, standards and GMP regulations.
  • Good understanding of Clinical Supplies packaging, labeling and distribution plus related paperwork.

Please visit GSK US Benefits Summary to learn more about the comprehensive benefits program GSK offers US employees.

Why GSK?

Uniting science, technology and talent to get ahead of disease together.

GSK is a global biopharma company with a special purpose - to unite science, technology and talent to get ahead of disease together - so we can positively impact the health of billions of people and deliver stronger, more sustainable shareholder returns - as an organisation where people can thrive. We prevent and treat disease with vaccines, specialty and general medicines. We focus on the science of the immune system and the use of new platform and data technologies, investing in four core therapeutic areas (infectious diseases, HIV, respiratory/ immunology and oncology).

Our success absolutely depends on our people. While getting ahead of disease together is about our ambition for patients and shareholders, it's also about making GSK a place where people can thrive. We want GSK to be a place where people feel inspired, encouraged and challenged to be the best they can be. A place where they can be themselves - feeling welcome, valued, and included. Where they can keep growing and look after their wellbeing. So, if you share our ambition, join us at this exciting moment in our journey to get Ahead Together.

If you require an accommodation or other assistance to apply for a job at GSK, please contact the GSK Service Centre at 1-877-694-7547 (US Toll Free) or +1 801 567 5155 (outside US).

GSK is an Equal Opportunity Employer and, in the US, we adhere to Affirmative Action principles. This ensures that all qualified applicants will receive equal consideration for employment without regard to race, color, national origin, religion, sex, pregnancy, marital status, sexual orientation, gender identity/expression, age, disability, genetic information, military service, covered/protected veteran status or any other federal, state or local protected class.

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Please note that if you are a US Licensed Healthcare Professional or Healthcare Professional as defined by the laws of the state issuing your license, GSK may be required to capture and report expenses GSK incurs, on your behalf, in the event you are afforded an interview for employment. This capture of applicable transfers of value is necessary to ensure GSK's compliance to all federal and state US Transparency requirements. For more information, please visit the Centers for Medicare and Medicaid Services (CMS) website at https://openpaymentsdata.cms.gov/

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