QC Chemistry Lead

B. Braun Medical Inc., a leader in infusion therapy and pain management, develops, manufactures, and markets innovative medical products and services to the healthcare industry. Other key product areas include nutrition, pharmacy admixture and compounding, ostomy and wound care, and dialysis. The company is committed to eliminating preventable treatment errors and enhancing patient, clinician and environmental safety.

B. Braun Medical is headquartered in Bethlehem, Pa., and is part of the

B. Braun Group of Companies in the U.S., which includes

B. Braun Interventional Systems, Aesculap® and CAPS®. Globally, the

B. Braun Group of Companies employs more than 64,000 employees in 64 countries. Guided by its Sharing Expertise® philosophy,

B. Braun continuously exchanges knowledge with customers, partners and clinicians to address the critical issues of improving care and lowering costs. To learn more about

B. Braun Medical, visit

The QC Chemistry Lead I performs and supports chemical laboratory activities for raw materials, in-process materials, environmental samples, finished products, stability samples, and other projects within the QC Chemistry Laboratory. This role conducts routine and non-routine testing, reviews analytical data, supports validation activities, and prepares quality documentation in accordance with established procedures and applicable cGMP/GLP requirements. The position also provides day-to-day peer support by assisting with training, work assignments, and review of completed work.

Regular and predictable onsite attendance is required.

• Perform sampling, sample login, analytical testing, data review, and validation activities for raw materials, in-process materials, environmental samples, finished products, stability samples, and other laboratory projects.
• Complete routine and non-routine chemistry assignments while following approved procedures, specifications, safety practices, and cGMP/GLP requirements.
• Prepare and update investigation reports, deviations, protocols, procedures, and other chemistry‑related documentation.
• Review laboratory data and documentation for accuracy, completeness, and compliance with established requirements.
• Assist with orienting and training peers, assigning work, and checking completed work as needed.
• Collaborate with laboratory leads, supervisors, peers, and internal partners to resolve day‑to‑day issues and maintain workflow.
• Support additional laboratory and quality responsibilities as assigned.

• High school diploma or equivalent required.
• A minimum of 4 years of related laboratory, quality control, chemistry, or testing experience.
• Ability to follow established procedures and complete routine, repetitive assignments within defined parameters.
• Working knowledge of laboratory documentation practices and the ability to apply sound judgment when resolving day‑to‑day problems.
• Ability to communicate and collaborate effectively with supervisors, leads, peers, and cross‑functional partners.
• Ability to work a non‑standard schedule as business needs require.

• Bachelor's degree in Chemistry or another science‑related field.
• Experience in a cGMP‑ or GLP‑regulated laboratory environment.
• Experience testing raw materials, in‑process materials, finished products, environmental samples, or stability samples.
• Experience supporting deviations, investigations, protocols, procedures, validation activities, or peer training.

• Regular and predictable onsite attendance in a laboratory environment, with occasional work in production or manufacturing areas.
• Light work that may require exerting up to 20 pounds of force…