Scientist II (Pharmaceutical Quality Control)

Location: Fort Washington, Pennsylvania, United States; onsite laboratory work

Company

hirify.global provides workforce solutions to customers across multiple industries in the United States and Canada.

What you will do

• Provide testing, technical, and troubleshooting support in quality control laboratories.
• Collect, process, develop methods for, and test chemical components, raw materials, packaging components, bulk products, finished products, and in-process materials.
• Support marketed product stability, scale-up, validation, cleaning validation, product release, and annual product reviews.
• Review and write SOPs, APRs, QSRs, instrument qualification documents, protocols, reports, and data-trending analyses.
• Participate in investigations, regulatory inspections, audits, training, and compliance activities.
• Lead or support continuous improvement, kaizen, change-management, and departmental coordination activities.

Requirements

• Bachelor’s degree in Microbiology, Chemistry, Biology, Natural Science, Medical Technology, or a related science.
• At least 2 years of GMP/GLP quality control laboratory experience in a pharmaceutical, OTC, or other regulated environment.
• Working knowledge of GMP requirements, SOPs, USP, and applicable pharmacopeia.
• Working knowledge of SAP or an ERP system, automated laboratory systems, electronic batch records, and Microsoft Office tools.
• Ability to perform routine laboratory activities and light to moderate lifting.

Culture & Benefits

• Work is performed in a regulated laboratory and manufacturing environment with required safety training and PPE.
• Participation in GMP, EHS, Lean, process-excellence, and continuous-improvement programs.
• Emphasis on integrity, compliance, teamwork, open communication, diversity, and inclusion.
• Contract duration: 12 months.