Skip to content
Updated How AI-exposed are the skills employers are hiring for? See the data →

From the employer's careers site First seen 7 Nov 2026

Biopharm Manufacturing Associate II

The employer hasn't listed a salary.

Apply on GSK

Description

As a Biopharm Manufacturing Associate II at GSK, you will perform production operations including fermentation or cell culture operations, preparation of solutions, chromatographic separation, filtration and concentration operations, autoclave and parts washing of process assemblies, and area cleaning/upkeep.

You will be responsible for completing daily manufacturing tasks, and increasing competency in different production areas over time. You will participate in safety and compliance initiatives, as well as investigations. You will engage in the GSK Production System to continuously improve safety, quality, and schedule/cost performance.

The role involves demonstrating GSK Values – Patient Focus, Transparency, Respect, and Integrity – in every interaction, and living GSK’s Expectations of Courage, Accountability, Development, and Teamwork to achieve high performing behaviors in the workplace.

Responsibilities include:

  • Safely and compliantly completing and documenting daily manufacturing tasks per standard operating procedures
  • Proactively working with senior staff to achieve competency in production operations
  • Supporting cross-functional activities, such as engineering actions, validation actions, and Tech Transfer actions
  • Monitoring equipment and critical process parameters, and escalating any issues or abnormalities
  • Striving to maintain a high level of competency with current and emerging digital platforms
  • Participating in investigations that are the result of safety or compliance issues

Basic qualifications:

  • BS/BA degree with cGMP manufacturing experience
  • OR an Associate’s degree from Montgomery county community college in Biotechnology or related technical field with cGMP manufacturing experience
  • OR High School degree, 1+ years of cGMP manufacturing experience

Preferred Qualifications:

  • Demonstrated level of high performance
  • Strong verbal and written skills
  • Ability to work well in a team environment
  • Must be able to follow detailed processing instructions and accurately document all necessary documentation

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

For more fresh new jobs, check out yubhub.co.

Skills

Required

  • Biopharmaceuticals
  • Bioprocessing
  • Cell Line Development
  • Experimental Methods
  • Technology Transfer

Nice to have

  • high performance
  • verbal and written skills
  • teamwork
  • documentation

Ready to apply?

You apply with the employer directly. Their original posting is here: https://gsk.wd5.myworkdayjobs.com/en-US/GSKCareers/job/USA---Pennsylvania---King-of-Prussia/Biomanufacturing-Associate-II_448948

Apply on GSK