QC Chemistry Lead I (Monday-Friday 10pm-6:30am)

B. Braun US Pharmaceutical Manufacturing LLC; Irvine (CA); On-site; USD 41,000 - 50,000; Full time

Benefits offered by this job

Healthcare

401(k) plan

Tuition reimbursement

Job summary

B. Braun Medical Inc. in Irvine, CA is seeking a QC Chemistry Lead I to perform and support chemical laboratory activities across raw materials, in-process materials, and environmental samples.

The role requires routine testing, data review, and adherence to cGMP/GLP requirements. You will train peers, review documentation, and collaborate with cross-functional teams to maintain workflow, all while onsite in a controlled laboratory environment.

Qualifications

• High school diploma or equivalent required.
• Minimum of 4 years of laboratory/quality control/chemistry/testing experience.
• Ability to follow established procedures and complete routine tasks.
• Effective communication with supervisors, leads, peers, and cross-functional partners.
• Ability to work a non-standard schedule as business needs require.
• Experience in a cGMP- or GLP-regulated laboratory environment (preferred).
• Bachelor's degree in Chemistry or another science-related field (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

Collaboration

Attention to detail

Problem solving

Time management

Education

High school diploma or equivalent

Bachelor's degree in Chemistry or related field

Job description

B. Braun Medical, Inc.

Company: B. Braun US Pharmaceutical Manufacturing LLC

Job Posting Location: Irvine, California, United States

Functional Area: Quality

Working Model: Onsite

Days of Work: Friday, Thursday, Wednesday, Tuesday, Monday

Shift: 5X8

Relocation Available: No

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 www.bbraunusa.com

Position Summary

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.

In This Role, You Will Have the Chance To

• 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.

Essential Requirements

• 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.

Preferred Experience Includes

• 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.

Work Environment and Physical Requirements

• 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 occasionally, up to 10 pounds frequently, or a negligible amount of force regularly to move objects.
• Frequent standing, sitting, walking, seeing, hearing, talking, and use of visual acuity with or without corrective lenses.
• Occasional handling, pushing, pulling, and reaching upward or downward.
• Occasional exposure to toxic or caustic chemicals; required personal protective equipment and safety procedures must be followed.
• Low noise intensity, with regular work in a laboratory setting.

Pay Range- $30.28 - $36.05 /hour

The targeted range for this role takes into account a range of factors that are considered when making compensation and hiring decisions; included but not limited to: skill sets; experience and training; licensure and certifications; and other business and organizational needs. The disclosed range estimate has not been adjusted for the applicable geographic differential associated with the location at which the position may be filled. Compensation decisions are dependent on the facts and circumstances of each case. The range provided is a reasonable estimate.

• B. Braun offers an excellent benefits package, which includes healthcare, a 401(k) plan, and tuition reimbursement.

To learn more about B. Braun and our safety healthcare products or view a listing of our employment opportunities, please visit us on the internet at www.bbraunusa.com.

Through its "Sharing Expertise®" initiative, B. Braun promotes best practices for continuous improvement of healthcare products and services.

We are an equal opportunity employer. We evaluate applications without regard to race, color, religion, sex, sexual orientation, gender identity, national origin, age, pregnancy, genetic information, disability, status as a protected veteran, or any other protected characteristic. Know Your Rights: Workplace Discrimination is Illegal, click here.

All qualified applicants will receive consideration for employment without regard to race, color, sex, sexual orientation, gender identity, religion, national origin, disability, veteran status, age, marital status, pregnancy, genetic information, or other legally protected status.

Equal employment opportunity, including veterans and individuals with disabilities.