Quality Control Analyst

ACTalent; Plainville (MA); On-site; USD 41,000 - 45,000; Full time

Benefits offered by this job

Medical, dental & vision

401(k) Retirement Plan

Paid time off

Job summary

Actalent is seeking an Analyst I, QC Microbiology for a contract role in Plainville, MA. You will perform routine microbiological testing and environmental monitoring to support manufacturing operations, assist with laboratory maintenance, data entry, and documentation while developing technical expertise under GMP.

Key responsibilities include environmental monitoring of classified areas, microbiological testing (bioburden, endotoxin, growth promotion, method suitability), and accurate data

Qualifications

• Bachelor's degree in Microbiology, Biology, Biotechnology, Biochemistry, or related Life Science.
• Equivalent combination of education and relevant laboratory experience may be considered.
• 12 years of experience in a GMP or regulated laboratory environment.
• Experience in GMP-regulated environment is required.
• Exposure to environmental monitoring, microbiological testing, aseptic techniques, or laboratory documentation is required.
• Basic knowledge of microbiology principles and GMP data integrity is preferred.

Responsibilities

• Perform routine environmental monitoring of classified manufacturing areas and critical utility sampling.
• Execute microbiological testing including bioburden, endotoxin, growth promotion, and method suitability testing.
• Accurately document laboratory activities and enter test results into LIMS and other electronic systems.
• Perform routine laboratory cleaning, organization, and preventative maintenance.
• Maintain laboratory inventory and ensure adequate stocking of supplies and consumables.
• Support investigation activities by gathering data for alert/action level excursions and deviations.
• Follow GMP documentation practices, SOPs, and safety requirements.
• Participate in training programs and contribute to continuous improvement within a collaborative team.

Skills

Environmental monitoring

Microbiology

Documentation

Data entry

Laboratory operations

Communication skills

Education

Bachelor's degree in Microbiology

Equivalent combination of education and experience

Tools

LIMS

Microsoft Office

Job description

Description

• SundayWednesday: 7:00 AM5:30 PM. Eligible for conversion based on performance and business needs.


• WednesdaySaturday: 7:00 AM5:30 PM. Eligible for conversion based on performance and business needs.

The Analyst I, QC Microbiology performs routine microbiological testing and environmental monitoring activities in support of manufacturing operations. The incumbent assists with laboratory maintenance, sample processing, data entry, and documentation while developing technical expertise and working closely with QC Microbiology team members to ensure compliance with GMP requirements.

Key Responsibilities

• Perform routine environmental monitoring of classified manufacturing areas and critical utility sampling in accordance with approved procedures.


• Execute microbiological testing, including bioburden, endotoxin, growth promotion, and method suitability testing under supervision and established procedures.


• Accurately document laboratory activities and enter test results into LIMS and other electronic systems.


• Perform routine laboratory cleaning, organization, and preventative maintenance activities.


• Maintain laboratory inventory and ensure adequate stocking of supplies and consumables.


• Support investigation activities by gathering data and providing information for alert/action level excursions and deviations.


• Follow GMP documentation practices, SOPs, work instructions, and safety requirements.


• Participate in training programs to develop technical and regulatory knowledge.


• Support continuous improvement initiatives and maintain a collaborative team environment.

Additional Skills & Qualifications

• Bachelors degree in Microbiology, Biology, Biotechnology, Biochemistry, or another related Life Science discipline.


• An equivalent combination of education and relevant laboratory experience may be considered.


• 12 years of experience in a GMP or regulated laboratory environment, including manufacturing, microbiology, quality control, pharmaceutical, or medical device settings.


• Experience working in a GMP-regulated environment is required.


• Exposure to environmental monitoring, microbiological testing, aseptic techniques, or laboratory documentation is required.


• Basic knowledge of microbiology principles, aseptic techniques, and laboratory practices.


• Understanding of GMP regulations, data integrity principles, and quality systems is preferred.


• Ability to perform routine environmental monitoring and microbiological testing following established procedures.


• Ability to accurately document laboratory activities and maintain compliant records.


• Basic computer skills, including Microsoft Office applications. Familiarity with LIMS is preferred.


• Strong attention to detail and organizational skills.


• Effective verbal and written communication skills.


• Ability to manage multiple tasks and adapt to changing priorities in a fast-paced environment.


• Ability to work collaboratively within a team and build effective working relationships.


• Demonstrated willingness to learn new techniques and develop technical expertise.


• Ability to identify and escalation issues in a timely manner while maintaining compliance with quality and safety requirements.


• Ability to gown and access classified cleanroom and utility areas while following aseptic and contamination control practices.


• Ability to perform routine laboratory activities requiring prolonged periods of standing, walking, and movement between manufacturing and laboratory areas.


• Ability to lift, carry, push, and pull materials and supplies weighing up to 25 lbs.


• Ability to perform repetitive tasks, including sample collection and data entry.

Job Type & Location

This is a Contract position based out of Plainville, MA.

Pay And Benefits

The pay range for this position is $30.00 - $33.00/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)

Job Type & Location

This is a Contract position based out of Plainville, MA.

Application Deadline

This position is anticipated to close on Nov 23, 2026.

Workplace Type

This is a fully onsite position in Plainville,MA.

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.