Microbiology Lab Technician

Actalent; Minnesota; On-site; USD 28,000 - 33,000; Full time

Benefits offered by this job

Medical, dental & vision

401(k) Retirement Plan

Paid time off

Job summary

Actalent in Saint Paul, MN is seeking an entry-level Lab Technician focused on microbiology and quality control within a regulated GMP environment. The role blends hands-on lab work with autoclave sterilization requalification and routine testing (pH, conductivity, solution prep) across medical device and pharmaceutical manufacturing.

You'll gain exposure to entry-level instrumentation, data systems (LIMS) and support production quality and compliance activities, while developing essential

Qualifications

• Bachelor’s degree in Microbiology or related field.
• Experience in GMP environments preferred.
• Familiarity with LIMS and data integrity practices.

Responsibilities

• Perform biological, chemical and physical testing on medical products and materials.
• Conduct environmental monitoring testing at manufacturing facilities.
• Set up test apparatus and ensure methods, standards and procedures comply with regulations.
• Carry out routine lab tasks including pH, conductivity, solution prep, autoclaving and glassware cleaning.
• Use laboratory instruments and LIMS to collect, record and review data accurately.
• Write deviation documentation and support out-of-spec investigations.
• Participate in cross-functional activities to improve quality and efficiency.

Skills

Microbiology

Lab testing

GMP

Education

Bachelor's degree in Microbiology or related field

Tools

LIMS

Autoclave

Job description

This entry-level lab technician role focuses on microbiology and quality control testing in a regulated GMP environment, with responsibilities split between laboratory duties and autoclave sterilization requalification. The position emphasizes routine, repetitive testing such as pH, conductivity, solution-related work, autoclaving, and glassware cleaning, while providing exposure to medical device and pharmaceutical (biologics and drugs) testing across the manufacturing process. The role offers hands-on experience with entry-level instrumentation and laboratory systems, supporting both production quality and compliance activities.

Job Description

This entry-level lab technician role focuses on microbiology and quality control testing in a regulated GMP environment, with responsibilities split between laboratory duties and autoclave sterilization requalification. The position emphasizes routine, repetitive testing such as pH, conductivity, solution-related work, autoclaving, and glassware cleaning, while providing exposure to medical device and pharmaceutical (biologics and drugs) testing across the manufacturing process. The role offers hands-on experience with entry-level instrumentation and laboratory systems, supporting both production quality and compliance activities.

Responsibilities

• Perform biological, chemical and physical testing on pharmaceutical products, medical devices and related materials from incoming raw materials through in-process and final products.
• Conduct testing on samples collected from environmental monitoring programs at manufacturing facilities.
• Set up test apparatus and conduct tests on production processes and products to ensure methods, procedures, standards and sequences of operations comply with legal, regulatory and internal policies.
• Carry out routine laboratory tasks including pH and conductivity measurements, solution preparation, autoclaving and glassware cleaning.
• Use laboratory instrumentation and computer systems, including LIMS, to collect, record and review data accurately and in a timely manner.
• Perform assays that require precise analytical skills and a solid understanding of biology and chemistry principles.
• Complete all assigned testing, including special project and protocol testing, within required timelines and according to procedures.
• Maintain data integrity and ensure compliance with SOPs, specifications and applicable regulations such as FDA, GLP, QSR and cGMP.
• Write exception documents and support documentation for deviations, out-of-specification and out-of-limit results as needed.
• Participate in cross-functional team activities that impact production, increase efficiency, solve problems, generate cost savings and improve quality.
• Perform laboratory and manufacturing audits as required, and assist in auditing and updating plant SOPs.

Essential Skills

• Bachelors degree (BS/BA) in Microbiology, Biology, Chemistry or a closely related field.

Job Type & Location

This is a Contract to Hire position based out of SAINT PAUL, MN.

Pay And Benefits

The pay range for this position is $22.00 - $22.00/hr.

Individual compensation offered for this position within this range will depend on many factors, including qualifications, skills, relevant experience, job knowledge, geographic location, internal equity, and other pertinent job-related factors.

Eligibility requirements apply to some benefits and may depend on your job classification and length of employment. Benefits are subject to change and may be subject to specific elections, plan, or program terms. If eligible, the benefits available for this temporary role may include the following: Medical, dental & vision Critical Illness, Accident, and Hospital 401(k) Retirement Plan Pre-tax and Roth post-tax contributions available Life Insurance (Voluntary Life & AD&D for the employee and dependents) Short and long-term disability Health Spending Account (HSA) Transportation benefits Employee Assistance Program Time Off/Leave (PTO, Vacation or Sick Leave)

Workplace Type

This is a fully onsite position in SAINT PAUL,MN.

Application Deadline

This position is anticipated to close on Oct 19, 2026.

About Actalent

Actalent is a global leader in engineering and sciences services and talent solutions. We help visionary companies advance their engineering and science initiatives through access to specialized experts who drive scale, innovation and speed to market. With a network of almost 20,000 consultants and 5,000 clients across the U.S., Canada, Asia and Europe, Actalent serves many of the Fortune 500. We are proud to be an Engineering News-Record (ENR) Top 500 Design Firm for our engineering design services and a ClearlyRated Best of Staffing® winner for both client and talent service.

The company is an equal opportunity employer and will consider all applications without regard to race, sex, age, color, religion, national origin, veteran status, disability, sexual orientation, gender identity, genetic information or any characteristic protected by law.

If you would like to request a reasonable accommodation, such as the modification or adjustment of the job application process or interviewing process due to a disability, please email [e-mail] for other accommodation options.

San Francisco Fair Chance Ordinance

Pursuant to the San Francisco Fair Chance Ordinance, for all positions located in the city and county of San Francisco, we will consider for employment qualified applicants with arrest and conviction records.

Massachusetts Lie Detector

It is unlawful in Massachusetts to require or administer a lie detector test as a condition of employment or continued employment. An employer who violates this law shall be subject to criminal penalties and civil liability.

Use of Artificial Intelligence (AI)

We may use Artificial Intelligence (AI) to support parts of our hiring process, including sourcing, screening, and evaluating candidates. AI helps assess applications and qualifications, but final decisions are made by our hiring team. By applying, you acknowledge and agree that your application may be reviewed using AI tools.