# Biopharm Manufacturing Associate II

**Company**: GSK
**Location**: King of Prussia, Pennsylvania
**Job type**: full-time
**Category**: Manufacturing
**Industry**: Healthcare

**Apply**: https://gsk.wd5.myworkdayjobs.com/en-US/GSKCareers/job/USA---Pennsylvania---King-of-Prussia/Biopharmaceutical-Manufacturing-Associate-II_450446?utm_source=yubhub.co&utm_medium=jobs_feed&utm_campaign=apply
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## 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 requires 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, batch document instructions, and logbooks

- Proactively working with senior staff to achieve competency in production operations

- Supporting in 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

- The ability to work well in a team environment

- Must be able to follow detailed processing instructions as well as accurately documenting all necessary documentation

## Skills

### Required
- Biopharmaceuticals
- Bioprocessing
- Cell Line Development
- Experimental Methods
- Technology Transfer

### Nice to have
- high performance
- verbal and written skills
- teamwork
- documentation

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