QC Chemistry Lead — Night Shift

B. Braun Group

Irvine (CA)

On-site

USD 41,000 - 50,000

Full time

2 days ago
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Job summary

B. Braun is hiring for a QC Chemistry Lead I at our Irvine, CA site. The role oversees chemistry lab activities for raw materials, in-process materials, and finished products, with emphasis on cGMP/GLP compliance and data integrity.

Expect routine and non-routine testing, data review, and validation support, plus training and mentoring of peers. This onsite position requires a strong attention to safety and documentation practices.

Qualifications

  • High school diploma or equivalent required.
  • Bachelor's degree in Chemistry or a related science preferred.

Responsibilities

  • 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.

Skills

Communication
Team collaboration
Attention to detail

Education

High school diploma or equivalent
Bachelor's degree in Chemistry

Job description

B. Braun is hiring for a QC Chemistry Lead I at our Irvine, CA site. The role oversees chemistry lab activities for raw materials, in-process materials, and finished products, with emphasis on cGMP/GLP compliance and data integrity.

Expect routine and non-routine testing, data review, and validation support, plus training and mentoring of peers. This onsite position requires a strong attention to safety and documentation practices.

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