QC Scientist
About the role
This position requires open availability
with the understanding that some weekend work will be required, additionally this role requires the ability to work independently while effectively collaborating across Quality, Manufacturing, and Technical Operations.
This role will provide YOU the opportunity to lead key activities to progress YOUR career, these responsibilities include some of the following:
- Perform routine and non-routine microbiological testing of: Raw materials, In-process samples, Drug substance, Drug product, EM/UM samples
- Execute Bioburden Testing and Bacterial Endotoxin Testing (BET) in accordance with approved procedures and compendial requirements.
- Perform testing to support product release, stability studies, validation activities, and manufacturing operations.
- Collect, test, review, and trend utility monitoring samples from pharmaceutical water systems, clean steam, and compressed gas systems.
- Escalate quality or compliance concerns promptly to management.
- Accurately document laboratory activities and results in compliance with cGMP, GDP, and ALCOA+ data integrity principles.
- Identify opportunities for process improvements and laboratory efficiencies.
- Perform routine laboratory housekeeping and inventory management activities.
- Support method qualifications, method transfers, equipment qualifications, and validation activities as assigned.
- Performs other duties as assigned.
Why you?
Basic Qualifications
We are looking for professionals with these required skills to achieve our goals:
- Bachelor's degree in microbiology, Biology, Biotechnology, or a related Life Science discipline with 3+ years of hands-on microbiology laboratory experience
•
OR
OR
master's degree in microbiology, Biology, or a related Life Science discipline with a minimum of 1 year of hands-on microbiology experience in a GMP-regulated environment.
- Experience working in a GMP/GxP-regulated pharmaceutical, biotechnology, medical device, or healthcare environment.
- Experience performing Bioburden and Bacterial Endotoxin Testing (BET).
Preferred Qualifications
If you have the following characteristics, it would be a plus:
- 3+ years of previous experience working in a GMP QC Microbiology Laboratory
- Advanced experience with testing microbiological compendial methods in line with: USP, EP, and JP requirements, ICH guidelines and FDA expectations.
- SAP or ERP, LES/LES-EM, LIMS, WebStatistica, Electronic Laboratory Notebook (ELN) systems, Veeva.
- Experience supporting investigations, CAPAs, deviations, and change controls.
#LI-GSK
Skills
Data Integrity, Detail-Oriented, Digital Fluency, GxP Regulations, Lean Management, Problem Solving, Quality Assurance (QA), Quality Control (QC), Risk Awareness, Testing Operations
Please visit GSK US Benefits Summary to learn more about the comprehensive benefits program GSK offers US employees.
Uniting science, technology and talent to get ahead of disease together.
Important notice to Employment businesses/ Agencies
Not included in the source posting: about the role, benefits.
Skills
Who can apply
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