Environmental Monitoring Analyst

Job Description

Job Description

Environmental Monitoring AnalystLaunch Your Career in Pharmaceutical Quality & Microbiology

Are you a recent science graduate looking to start a rewarding career in the pharmaceutical or biotechnology industry? The Environmental Monitoring Analyst role is an excellent opportunity to gain hands-on experience in Quality Control, Microbiology, and GMP manufacturing while contributing directly to the production of life-changing medicines.

In this role, you'll receive extensive training and mentorship as you learn how pharmaceutical facilities maintain sterile manufacturing environments and ensure the highest standards of product quality and patient safety. You'll work alongside experienced professionals in Quality, Manufacturing, and Laboratory Operations, developing highly sought-after skills that can lead to future opportunities in Microbiology, Quality Assurance, Quality Control, Validation, and other pharmaceutical science careers.

• Perform environmental monitoring activities throughout pharmaceutical manufacturing and laboratory areas to ensure cleanroom and facility compliance.
• Collect viable and non-viable air, surface, water, and utility samples used to evaluate contamination control programs.
• Incubate and analyze microbiological samples, interpret results, and document findings in electronic quality systems.
• Learn and apply industry-leading Good Manufacturing Practices (GMPs) and aseptic techniques used in regulated pharmaceutical environments.
• Support routine monitoring of cleanrooms, water systems, compressed gases, and other critical utilities that help ensure product quality and patient safety.
• Maintain accurate electronic documentation in compliance with pharmaceutical data integrity standards.
• Collaborate with Quality, Manufacturing, and Laboratory teams to investigate observations and maintain a state of control within the facility.
• Participate in ongoing training programs designed to develop expertise in environmental monitoring, microbiology, and pharmaceutical quality systems.
• Contribute to a culture of quality, compliance, teamwork, and continuous improvement.

• Strong training program with hands-on mentorship from experienced scientists and quality professionals.
• Opportunity to apply classroom knowledge in microbiology, biology, chemistry, and pharmaceutical sciences in a real-world GMP environment.
• Exposure to pharmaceutical manufacturing, microbiology testing, contamination control, and quality systems.
• Build foundational industry experience that can lead to advancement in Quality Control, Quality Assurance, Microbiology, Validation, Manufacturing Sciences, and other life sciences career paths.
• Work for an organization focused on innovation, patient safety, and professional development.

• Bachelor's degree in Biology, Microbiology, Chemistry, Pharmaceutical Sciences, Environmental Science, or a related scientific discipline.
• Recent graduates are encouraged to apply.
• Strong attention to detail and a passion for science, quality, and problem-solving.
• Interest in pharmaceutical manufacturing, microbiology, or quality control.
• Excellent communication and organizational skills.
• Ability to learn quickly, follow procedures, and thrive in a team-oriented environment.

• Internship, co-op, academic laboratory, research, or industry experience.
• Exposure to microbiology techniques, sample processing, or environmental monitoring.
• Familiarity with GMPs, aseptic technique, or pharmaceutical manufacturing environments.
• Experience using electronic data management or laboratory systems.

This position offers hands-on experience in both laboratory and pharmaceutical manufacturing environments. You'll spend time throughout the facility performing monitoring activities while working closely with a supportive team dedicated to quality, safety, and professional growth. The schedule is Monday through Friday, approximately 8:00 AM to 4:30 PM, providing a consistent work-life balance while building a strong foundation for a long-term career in the life sciences industry.

If you're looking for a meaningful opportunity to break into the pharmaceutical industry and build a career in Quality and Microbiology, we'd love to hear from you.

This is a Contract position based out of Raleigh, NC.

The pay range for this position is $25.00 - $25.00/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)

This is a fully onsite position in Raleigh,NC.

This position is anticipated to close on Sep 16, 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 withoutregard to race, sex, age, color, religion, national origin, veteran status, disability,sexual orientation, gender identity, genetic information or any characteristic protectedby law.

If you would like to request a reasonable accommodation, such as the modification oradjustment of the job application process or interviewing process due to a disability,please email View email address on ziprecruiter.com for other accommodation options.

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

Massachusetts Lie Detector: It is unlawful in Massachusetts to require or administer a lie detector test as acondition of employment or continued employment. An employer who violates this lawshall 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 applicationsand qualifications, but final decisions are made by our hiring team. By applying, youacknowledge and agree that your application may be reviewed using AI tools.