Microbiology and Sterilization Analyst

Becton Dickinson; Sandy (UT); On-site; USD 65,000 - 90,000; Full time

Job summary

Becton Dickinson is seeking a QA Laboratory professional in Utah to support microbiological testing, environmental monitoring, and sterilization assurance. The role ensures product quality, patient safety, and regulatory compliance through accurate documentation and adherence to GMP and GDP.

Schedule is Monday–Friday, 9:00 AM–5:30 PM with potential overtime as needed. Responsibilities include EO sterilization testing, GC-FID residual analysis, aseptic handling of cultures, data investigation,

Qualifications

• Associate degree or equivalent in Biology, Microbiology, Chemistry, Biotechnology, Life Sciences, Engineering, or related STEM field.
• Bachelor's degree in STEM with laboratory/regulated industry experience also eligible.
• Strong attention to detail with ability to document and analyze data.
• Ability to work safely in lab and cleanroom environments.

Responsibilities

• Perform microbiological testing on raw materials, finished products, and manufacturing environments.
• Conduct environmental monitoring in classified cleanrooms and GMP areas.
• Support sterilization assurance programs and EO sterilization testing.
• Perform EO/ECH residual testing using GC-FID on terminally sterilized devices.
• Aseptically handle microbial cultures and samples and maintain documentation.
• Investigate results, analyze data, and prepare technical reports.
• Create and maintain SOPs and lab forms.
• Ensure equipment readiness and maintain supplies; comply with GMP/GDP and safety rules.

Skills

Attention to detail

Lab safety

MS Office

Communication skills

GMP/GDP knowledge

Education

Associate degree in STEM

Bachelor's degree in STEM

Tools

Gas Chromatography (GC-FID)

Job description

We are the people who give possibilities purpose BD is one of the largest global medical technology companies in the world. Advancing the world of health™ is our Purpose, and it’s no small feat. It takes the imagination and passion of all of us—from design and engineering to the manufacturing and marketing of our billions of MedTech products per year—to look at the impossible and find transformative solutions that turn dreams into possibilities.

Job Description Support the Quality Assurance Laboratory through microbiological testing, environmental monitoring, and sterilization assurance activities to ensure product quality, patient safety, and regulatory compliance. Perform testing of raw materials, finished products, manufacturing environments, and sterilization processes while maintaining accurate documentation in accordance with GMP, GDP, and quality system requirements.

Schedule: Monday through Friday, 9:00 AM to 5:30 PM. Additional hours may be required based on business needs.

KEY RESPONSIBILITIES

• Perform microbiological testing on raw materials, finished products, and manufacturing environments to ensure compliance with quality specifications.
• Conduct environmental monitoring activities in classified cleanrooms and GMP manufacturing areas.
• Support sterilization assurance programs, including protocol execution and testing associated with ethylene oxide (EO) sterilization processes.
• Perform EO/ECH residual testing on terminally sterilized medical devices using gas chromatography (GC-FID).
• Aseptically handle microbial cultures and laboratory samples following established procedures.
• Investigate test results, analyze data, and prepare technical reports.
• Create, revise, and maintain Standard Operating Procedures (SOPs), laboratory forms, and related documentation.
• Verify laboratory equipment and maintain laboratory supplies, chemicals, and inventory.
• Maintain compliance with GMP, GDP, safety, environmental, and quality system requirements.
• Communicate results, observations, and issues effectively with laboratory, quality, and manufacturing teams.
• Support continuous improvement initiatives and perform other duties as assigned.

QUALIFICATIONS

Candidates must have an associate degree or equivalent background in STEM areas including Biology, Microbiology, Chemistry, Biotechnology, Life Sciences, Engineering, or another scientific field. Alternatively, individuals holding a bachelor's degree or equivalent experience in a STEM subject along with laboratory, manufacturing, quality, or regulated industry experience are eligible.

• Strong attention to detail with the ability to accurately document and analyze laboratory data.
• Ability to work safely and effectively in laboratory and cleanroom environments.
• Strong written and verbal communication skills.
• Proficiency with Microsoft Office applications.

Preferred Qualifications

• Experience in a microbiology, quality, pharmaceutical, medical device, biotechnology, laboratory, or other regulated manufacturing environment.
• Experience working in GMP and/or cleanroom environments.
• Experience conducting microbial evaluations, environmental assessments, sterilization processes, and/or gas chromatography.
• Knowledge of laboratory investigations, technical report writing, and quality systems.
• Strong analytical and problem-solving skills with the ability to work independently and collaborate effectively with cross-functional teams.

At BD, we prioritize on-site collaboration because we believe it fosters creativity, innovation, and effective problem-solving, which are essential in the fast-paced healthcare industry.

For most roles, we require a minimum of 4 days of in-office presence per week to maintain our culture of excellence and ensure smooth operations, while also recognizing the importance of flexibility and work-life balance. Remote or field-based positions will have different workplace arrangements which will be indicated in the job posting.

For certain roles at BD, employment is contingent upon the Company’s receipt of sufficient proof that you are fully vaccinated against COVID-19. In some locations, testing for COVID-19 may be available and/or required.

Consistent with BD’s Workplace Accommodations Policy, requests for accommodation will be considered pursuant to applicable law.

#earlycareer Why Join Us?

To find purpose in the possibilities, we need people who can see the bigger picture, who understand the human story that underpins everything we do. We welcome people with the imagination and drive to help us reinvent the future of healthcare. At BD, you’ll discover a culture in which you can learn, grow and thrive. We believe that when people connect in person, we learn faster, collaborate more deeply, and build a stronger culture. Join us and enjoy a culture where face‑to‑face collaboration supports your learning, your progress, and your success. To learn more about BD visit https://bd.com/careers.

Becton, Dickinson, and Company is an Equal Opportunity Employer. We evaluate applicants without regard to race, color, religion, age, sex, creed, national origin, ancestry, citizenship status, marital or domestic or civil union status, familial status, affectional or sexual orientation, gender identity or expression, genetics, disability, military eligibility or veteran status, and other legally protected characteristics.

Required Skills Communication, Documentations, Ensure Compliance, Good Manufacturing Practices (GMP), Laboratory Instrumentation, Laboratory Safety, Safety Standards, Standard Operating Procedure (SOP) Optional Skills Chemicals, Hazardous Wastes, Laboratory Glassware, Raw Materials, Sterilization . Primary Work Location USA UT - Sandy Additional Locations Work Shift PR 900am-530pm M-F (United States of America)

We are the #MakersofPossible Working together, we make products that patients, families and their healthcare professionals rely on. We do this because we are committed to advancing the world of health™. But it takes the imagination and passion of all of us at BD, from manufacturing to marketing, to look at the impossible and find solutions that turn dreams into possibilities with real‑life health benefits for people today, tomorrow and beyond. We make this happen, together. We are the makers of possible.

Becton, Dickinson and Company is an Equal Opportunity Employer. We evaluate applicants without regard to race, color, religion, age, sex, creed, national origin, ancestry, citizenship status, marital or domestic or civil union status, familial status, affectional or sexual orientation, gender identity or expression, genetics, disability, military eligibility or veteran status, and other legally-protected characteristics.