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MICROBIOLOGIST-I (Afternoon Shift Monday to Friday 15:00 - 23:00)

Baxter Corporation CAN
Full-time
On-site
Alliston, Canada

This is where you save and sustain lives

At Baxter, we are deeply connected by our mission. No matter your role at Baxter, your work makes a positive impact on people around the world. You'll feel a sense of purpose throughout the organization, as we know our work improves outcomes for millions of patients.

Baxter's products and therapies are found in almost every hospital worldwide, in clinics and in the home. For over 85 years, we have pioneered significant medical innovations that transform healthcare.

Together, we create a place where we are happy, successful and inspire each other. This is where you can do your best work.

Join us at the intersection of saving and sustaining livesβ€”where your purpose accelerates our mission.

We are in search of a Microbiologist-I to join our team at Baxter on our Afternoon Shift (Monday to Friday 15:00 - 23:00). This outstanding opportunity provides the chance to work in a dynamic environment where your contribution has a direct impact on patient safety and product quality.

General expectations

The top two priorities for all Baxter Alliston employees are Safety and Quality:

**Safety:** Support our goal to achieve a "Zero Harm Environment," by ensuring the safety of yourself and your co-workers through:

  • Following all safety procedures
  • Understanding potential hazards in your area
  • Wearing appropriate PPE
  • Reporting all incidents/near-misses/concerns
  • Embracing 6s

**Quality:** Ensure the quality of our products to ensure patient safety and achieve our mission of "Saving and Sustaining Lives." This can be achieved through:

  • Following Good Manufacturing Practices (GMP)
  • Adhering to all quality procedures
  • Completing training in a timely manner
  • Doing it Right the First Time, and
  • Reporting any quality concerns immediately

As part of the plant's Enterprise Management System (EMS), all employees must embrace a culture of Continuous Improvement by:

  • Participating in improvement activities
  • Identifying and implementing continuous improvement ideas
  • Participating in Tier meetings
  • Recognizing your peers, and
  • Embracing 6s
  • Identifying and implementing VIP's (Value Improvement Project)
  • Embracing continuous learning
  • Applying Leader Standard Work
  • Applying Root Cause Analysis tools to identify and prevent problems from recurring and drive measurable results

Essential duties and responsibilities

  • Collect water, air, and surface samples at assigned sites in the facility regularly for the Environmental Monitoring program. Perform necessary testing, incubation, and plate reading as per specifications.
  • Perform daily solution bioburden testing for total count and spore count. Use approved procedures. Complete required documentation. Read all results promptly. Also, conduct testing of raw materials.
  • Perform processing of biological indicators to support sterilizer qualifications.
  • Perform daily endotoxin and subvisible particulate testing of finished goods as per approved procedures and specifications.
  • Complete testing and documentation for critical work requests and emergency response incidents. This ensures timely production start-up after the work or incident.
  • Prepare and/or perform growth promotion testing on prepared or purchased media.

Job requirements

Education/ExperienceRequired:

  • College diploma or University Degree in a related field (Microbiology)

Preferred:

  • University Degree or equivalent experience, B.Sc. designation

Major Subjects / SpecialtiesRequired:

  • Microbiology
  • Quality Assurance

Type of ExperienceRequired:

  • Experience in a manufacturing environment
  • Proficiency in Word & Excel
  • Previous experience working in a Quality function
  • Knowledge of Aseptic Technique and Microbiological Methods

Preferred:

  • Previous experience with Laboratory Information Management System (LIMS)
  • Microbiological testing lab experience in the pharmaceutical industry
  • Knowledge of GMP, ISO standards, and regulatory/corporate requirements

Years of ExperienceRequired:

- 0 - 2 years

Preferred:

  • 2 + years

Additional Skills / Special Training / Technical SkillsRequired:

  • Strong analytical and problem-solving skills and critical thinking abilities
  • Strong communication skills, ability to work with all levels of the organization
  • Strong ability to balance multiple priorities with excellent time management skills
  • Diligent with the ability to work under pressure
  • Uncompromising dedication to quality
  • Ability to work off shift, holidays, and plant shut downs on a rotating basis
  • Coverage for production overtime Saturdays on a rotating basis is mandatory
  • Must align with Good Laboratory Practices
  • When performing Sterilizer Quals: the work is conducted in extreme environmental conditions (temperature, humidity, wet, moving trucks, loud, hot pipes)

Preferred:

  • Understanding of EMS through the application of LEAN tools in a laboratory environment
  • Technical writing skills

Reasonable Accommodations

Baxter is committed to working with and providing reasonable accommodations to individuals with disabilities globally. If, because of a medical condition or disability, you need a reasonable accommodation for any part of the application or interview process, please click on the link here and let us know the nature of your request along with your contact information.

Recruitment Fraud Notice

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