Jobs in Pennsylvania 2026 (Now Hiring) - Smart Auto Apply

• Perform cGMP material inspection for all materials utilized for drug product manufacturing.
• Perform cGMP material testing for all materials needed for further use in manufacturing process.
• Review analytical data for compliance with regulations, methods and other specifications or criteria and collaborate with management when data does not meet acceptance criteria.
• Participate in laboratory investigations, quality event investigations, protocol and report development.
• Initiate and update quality control documentation, such as SOPs, material monographs (specification and testing documents), and test methods. 
• Support activities for Document Control and Record Retention.
• Implementation of USP Quality Standards and verification of USP Methods.
• Maintain equipment in the QC Lab by performing and coordinating equipment qualification, calibration, and preventive maintenance.
• Other duties as assigned.

• Bachelor’s degree in life sciences or equivalent.
• Experience with pH, Osmo, Endotoxin, Appearance, customized media, cell culture, and FBS testing, preferred.
• Demonstrated experience in laboratory environment and ability to follow SOPs. 
• A demonstrated self-starter who is highly motivated and able to address changing priorities.
• Ability to take a proactive approach on the job with the ability to work with a dynamic team.
• Excellent scientific writing, other written and oral communication skills are required.
• Proficient in Microsoft Word, Excel and PowerPoint. 

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