249 Environmental Monitoring jobs in the United States

Environmental Monitoring Technician

Perform routine environmental monitoring of aseptic processing and controlled area cleanroom environments used for pharmaceutical manufacturing. Perform assigned quality control or quality assurance activities in compliance with applicable SOP's and cGMPs.

Schedule: Combination of 1st and 2nd shift, 5-week rotating schedule repeating the following schedule: Week 1: Mon-Th Week 2: Sat , Sun-Wed Week 3: Sun , Mon-Thur Weeks 4-5: Mon-Fri

Requirements

• Ensure a safe and quality working environment through training, awareness, and compliance with Safety/Quality guidelines and SOP's.
• Must maintain operational compliance with US and international regulatory agencies and guidelines (i.e. FDA, EU, HC, TGA, PIC/S, ISO, USP, NRC, cGMP, etc.).
• Ensure the maintenance of the department, premises, and equipment.
• Ensure that all necessary testing is carried out by required due dates. Perform all assigned tasks confidently and consistently.
• Perform monitoring using lab equipment and techniques (SAS, SMA, Met One particle counter, viable airborne monitoring (active and passive), total airborne particulate sampling, viable surface monitoring, personnel monitoring, and membrane filtration of water samples). Ensure assigned tasks are performed confidently and consistently.
• Ensure the use of proper aseptic technique during testing of controlled environments and utility systems.
• Perform all work in compliance with site quality, site safety and radiation protection guidelines. Collaborate with team members to ensure quality tasks is performed in a timely manner.
• Must demonstrate flexibility in adjusting to changing priorities and schedules.
• Attend mandatory training as required by site regulatory requirements and management. Assist with investigations.
• Perform other general duties associated with the position as required by supervision.

Essential Functions

• Associate degree or completion of college-level life science courses required. Work experience is considered in lieu of degree.
• Relevant experience preferred.
• Good interpersonal, hands on, analytical, problem solving and decision-making skills.
• Excellent writing and verbal communications skills.
• Good computer skills, including utilizing personal computers and data entry programs.
• Ability to work independently and with others to accomplish goals and priorities.
• Flexibility and teamwork skills, high level of energy and regular, consistent attendance.

Working Conditions:

• Willingness to work in plant producing radioactive materials and requiring all employees to participate in safety programs designed to minimize potential and/or actual exposure levels.
• Responsibilities include the ability to lift up to 70 pounds, kneeling, crouching, twisting the upper body, walking, bending, stooping, pushing, pulling, reaching, must be able to physically negotiate stairs and evacuation ladders with or without accommodation, wear and operate safety equipment, enter vessels, and inspect equipment.
• Material handling devices (e.g., hand truck, fork truck, and conveyors) are used when possible, however, use of proper lifting and movement techniques is necessary to prevent injury.
• Must be willing to wear a variety of Personal Protective Equipment (PPE) and hearing protection as needed.
• May be required to sit or stand for long periods of 8+ hours a day while performing duties.
• Must possess good hand-eye coordination; close attention to detail is required.
• Must be able to work indoors and outdoors with exposure to mechanical/moving parts, hazards including corrosive, flammable and toxic material, dust, dirt, odors, and irritants.
• Willingness to complete safety training within allotted timeframes, and work in a team-based environment.
• Must be able to work outside of regular work hours, including off shift, weekend, and holiday work as business needs require.

Disclaimer

The above statements are intended to describe the general nature and level of work being performed by employees assigned to this classification. They are not intended to be construed as an exhaustive list of all responsibilities, duties and skills required of employees assigned to this position.

Equal Opportunity Employer

Curium is an equal opportunity employer and believes everyone deserves respect, dignity and equality. All applicants will be considered for employment without attention to race, color, religion, sex, sexual orientation, gender identity, national origin, veteran or disability status.

Environmental Monitoring Technician

Location: Totowa, New Jersey

Department: Radiopharmaceutical Contract Manufacturing

Overview: The Microbiology - Environmental Monitoring Technician supports microbiology and manufacturing activities at the NJ5 site by (1) performing Environmental Monitoring (EM) as per sampling schedules (2) detecting, quantifying, identifying, and aiding in investigations for possible contaminants that may impact the quality of product during different stages of the manufacturing process.

Essential Duties and Responsibilities:

• Provide Environmental Monitoring (EM) support to GMP manufacturing areas. Perform EM testing for Active and Passive (settle plate) monitoring of Viable Particulates (Viable Air and Viable Surface RODAC), and Non-Viable Total Particulates.
• Follow EM sampling schedules in accordance with procedures, performing sampling of rooms and equipment.
• Perform EM sample management from incubation through isolate ID and completion of EM documentation.
• Work independently and with cross-functional groups to implement the environmental monitoring program to ensure the compliance of facility.
• Aid in EM investigations to determine root cause and provide expert guidance on required corrective actions for EM excursions.
• Assist in Growth Promotion conduction as necessary for EM related media.
• Support Microbiology team in the conduction of trending EM and relevant Out of Specification (OOS) data against acceptance specifications.
• Notify Microbiology/ EM Supervisor, Quality Control Manager, and Facility Manager of any identification of all microbial contamination.
• Support finished product release by checking results for sterility, endotoxin, and particulate matter testing (as required).
• Maintain aseptic environment for Microbiology and Stability laboratories, including regular maintenance of all equipment pertaining to EM.
• Disposal of hazardous waste and non-hazardous waste from Microbiology / Stability laboratories.
• Interact with management to suggest approaches to increase efficiency that will allow for better operations in the laboratory.
• Follow compliance to all applicable standard operating procedures and regulations, including 21 CFR Part 211 and 212 requirements.
• Other responsibilities required.

Qualifications:

• Bachelor's Degree in a Life Science discipline (B.Sc. in biology/ microbiology or related field preferred) and 0-3 years in a cGMP laboratory/ production environment including performing environmental monitoring.
• Knowledge of and previous experience performing Environmental Monitoring is preferred.
• Knowledge of USP, FDA, and cGMP regulations preferred.
• Knowledge of how and ability to write, review, and revise SOPs required.
• Ability to read, analyze, and interpret governmental regulations, professional journals, or technical procedures required.
• Ability to read and interpret documents such as safety rules, operating and maintenance instructions, and procedure manuals required.
• Ability to define and solve problems, collect data, establish facts, and draw valid conclusions required.
• Proficiency in MS Office applications required.
• Strong interpersonal communication skills for interacting with site personnel in both quality and manufacturing.

Piper Companies is currently looking for an experienced Environmental Monitoring Technician in Branchburg, New Jersey (NJ) to work for an innovative a growing pharmaceutical company.

Responsibilities for the Environmental Monitoring Technician include:
• Conduct laboratory sampling with in a gowned aseptic manufacturing environment in accordance with FDA/GMP regulations and company standards
• Provide environmental assistance to manufacturing and EM testing groups
• Maintain detailed laboratory documentation in accordance with GDP standards
• Cross trains to assist other functional quality areas including but not limited to deviation management, environmental monitoring investigations, and inspection support

Qualifications for the Environmental Monitoring Technician include:
• B.S. in Biology, Microbiology, or related field
• Experience working within a clean room environment
• Experience with taking samples, transporting samples and maintaining laboratory documentation

Compensation for the Environmental Monitoring Technician include:
• Salary Range is dependent upon experience
• Comprehensive benefits package

Keywords

Environmental Monitoring, Pharmaceutical Manufacturing, Science, Microbiology, Biology, Sampling, FDA, GMP, Biology, Comprehensive Benefits Package, Health, Vision, Dental

Geo-Logic Associates (GLA) is an employee-owned, multidisciplinary, civil, geologic, geotechnical, hydrogeologic, and environmental consulting firm. The firm was established in 1991 and currently operates out of 29 US office locations and an affiliate office in Peru. GLA is currently seeking a full-time Environmental Monitoring Technician (Technician) to provide support for civil/site infrastructure, solid waste, mining, and environmental evaluation and remediation projects in GLA's Riverside, California field office.

Candidate will be expected to work away from home on a regular basis. Work will include daily travel, working at remote sites, and interaction with team members, clients, contractors, and the general public. Candidate will regularly work at municipal solid waste disposal sites, hazardous waste sites, and mine sites. The Candidate must be able to lift up to 50 pounds. Employment is subject to a pre-employment physical examination, including drug screening.

Office Location: Riverside, California

The Technician will be expected to provide sample collection, field observation, and documentation at landfills, mine sites, public works construction sites, and other similar project sites. The work shall include, but not be limited to:

• Collecting groundwater, stormwater, surface water, leachate, landfill gas condensate, septage, soil-pore gas, and soil samples
• Calibrating and decontaminating field equipment
• Preparing samples for shipment
• Coordinating with laboratory personnel for delivery of sample containers and pick-up of samples
• Preparing chain-of-custody records
• Routine inspection and documentation of groundwater treatment systems
• Other tasks to support GLA's environmental monitoring programs.

Position requirements include:

• Be eligible to work in the United States
• Maintain a driving record acceptable to our insurer

Preferred skills include:

• OSHA 40-hour HAZWOPER training and current 8-hour annual HAZWOPER training
• MSHA training
• Undergraduate studies in physical science, environmental studies, or a related field.
• Familiarity with groundwater, surface water, and soil-pore gas sampling techniques, including standard purge (dedicated and non-dedicated equipment), low flow purge, grab sampling using bailers and passive diffusion devices

GLA offers a comprehensive benefits package including health/dental/vision insurance, 401(k) retirement plan, life insurance, flexible spending accounts, vacation leave, sick leave and profit sharing.

Click "Apply" below to submit your cover letter, resume and application. Applicants who are unable to apply online may submit their resume and cover letter by mail to: Human Resources, Geo-Logic Associates, 2777 East Guasti Road, Suite 1 Ontario, CA 91761. (Resumes submitted through postal mail must indicate reference Requisition #1072 on the front of the mailing envelope).

GLA is an Equal Opportunity Employer. All qualified applicants will receive consideration for employment without regard to age, race, color, religion, sex, national origin, sexual orientation, gender identity, disability and protected veterans status or any other characteristic protected by law.

**Job Title:** Environmental Monitoring (EM) Analyst - Contract
**Location:** Winston-Salem, North Carolina
**Schedule:** Monday-Friday, 8:00 AM - 5:00 PM
**Pay Rate:** $23-$26/hour | **Employment Type:** Contract
**Position Summary:** A contract opportunity is available for an Environmental Monitoring (EM) Analyst to support a cGMP-compliant facility. This role is responsible for performing routine environmental and utility monitoring, working alongside manufacturing teams, and maintaining strict compliance with regulatory and documentation standards.
**Key Responsibilities:** Conduct routine environmental monitoring of controlled cleanroom areas; perform personnel monitoring during manufacturing operations; operate EM equipment in accordance with established procedures; follow all SOPs, Work Instructions, and regulatory protocols; participate in training, revisions, and reviews of controlled documents; assist with sample receipt from manufacturing for QC Microbiology; track and trend EM, Bioburden, Sterility, and Endotoxin data; manage inventory in QC labs and coordinate with warehouse for material requests; perform streaking and isolation of recovered organisms; complete all documentation accurately and on time; support additional lab and monitoring duties as needed.
**Minimum Qualifications:**
**Education:** AS or BS in Life Sciences preferred
**Experience:** 1-3 years of relevant industry experience, with a minimum of 1 year in microbiological testing or environmental monitoring; prior GMP or cleanroom experience strongly preferred.
**Skills & Knowledge:** Basic understanding of GMP regulations and cleanroom behavior; familiarity with microbiology lab practices a plus; ability to follow schedules, procedures, and documentation requirements; strong organizational skills and attention to detail; ability to work independently and within a team; proficient in Microsoft Office (Excel, Word, Visio, etc.); good manual dexterity and ability to lift up to 30 pounds; effective communication skills (verbal and written); dependable with a strong work ethic.
As part of our promise to talent, Kelly supports those who work with us through a variety of benefits, perks, and work-related resources. Kelly offers eligible employees voluntary benefit plans including medical, dental, vision, telemedicine, term life, whole life, accident insurance, critical illness, a legal plan, and short-term disability. As a Kelly employee, you will have access to a retirement savings plan, service bonus and holiday pay plans (earn up to eight paid holidays per benefit year), and a transit spending account. In addition, employees are entitled to earn paid sick leave under the applicable state or local plan. Click here ( for more information on benefits and perks that may be available to you as a member of the Kelly Talent Community.
Why Kelly ® Science & Clinical?
Kelly Science & Clinical is your connection to premier scientific and clinical companies looking to hire industry experts just like you. Our team creates expert talent solutions to solve the world's most critical challenges. Every day, we match science professionals with dream jobs that fit their skills, interests, and career goals-it's the way we think job searching should be. Nearly 100 percent of our science recruiters have a professional background and education in science, so we know a thing or two about the science market and how to get your expertise noticed.
About Kelly
Work changes everything. And at Kelly, we're obsessed with where it can take you. To us, it's about more than simply accepting your next job opportunity. It's the fuel that powers every next step of your life. It's the ripple effect that changes and improves everything for your family, your community, and the world. Which is why, here at Kelly, we are dedicated to providing you with limitless opportunities to enrich your life-just ask the 300,000 people we employ each year.
Kelly is committed to providing equal employment opportunities to all qualified employees and applicants regardless of race, color, sex, sexual orientation, gender identity, religion, national origin, disability, veteran status, age, marital status, pregnancy, genetic information, or any other legally protected status, and we take affirmative action to recruit, employ, and advance qualified individuals with disabilities and protected veterans in the workforce. Requests for accommodation related to our application process can be directed to the Kelly Human Resource Knowledge Center. Kelly complies with the requirements of California's state and local Fair Chance laws. A conviction does not automatically bar individuals from employment. Kelly participates in E-Verify and will provide the federal government with your Form I-9 information to confirm that you are authorized to work in the U.S.
Kelly Services is proud to be an Equal Employment Opportunity and Affirmative Action employer. We welcome, value, and embrace diversity at all levels and are committed to building a team that is inclusive of a variety of backgrounds, communities, perspectives, and abilities. At Kelly, we believe that the more inclusive we are, the better services we can provide. Requests for accommodation related to our application process can be directed to Kelly's Human Resource Knowledge Center. Kelly complies with the requirements of California's state and local Fair Chance laws. A conviction does not automatically bar individuals from employment.

Job Title: Environmental Monitoring Analyst
Job Description
The Environmental Monitoring Analyst will conduct routine environmental monitoring of GMP areas and perform personnel monitoring for manufacturing operations. The role involves setting up and operating environmental monitoring equipment, following and executing standard operating procedures, work instructions, and protocols. Additionally, the analyst will perform reading, revising, and training on SOPs, work instructions, forms, and protocols, and support QC Micro Analyst in sample receipt from manufacturing.
Responsibilities
+ Conduct routine environmental monitoring of GMP areas.
+ Perform personnel monitoring for manufacturing operations.
+ Set up and operate environmental monitoring equipment.
+ Follow and execute standard operating procedures, work instructions, and protocols.
+ Perform reading, revising, and training on SOPs, work instructions, forms, and protocols.
+ Support QC Micro Analyst in sample receipt from manufacturing.
+ Track and trend environmental monitoring, bioburden, sterility, and endotoxin data collected.
+ Perform inventory stocking in the QC labs and request new materials from the warehouse.
+ Streak and isolate recovered organisms.
Essential Skills
+ Aseptic techniques
+ Environmental monitoring
+ Microbiology
+ GMP knowledge
+ Laboratory skills
+ Biology
+ Cell culture
+ Sterile and cleanroom experience
+ Quality control
+ Pipetting
+ Bench chemistry
+ Audit and quality assurance
Additional Skills & Qualifications
+ AS/BS in a science field (life sciences preferred)
+ 1-3 years of prior environmental monitoring experience in the biotech or pharma industry
+ BioWorks certification with 0-2 years of GMP experience considered
+ Cleanroom experience required
+ Knowledge in cell culture and aseptic techniques preferred
+ Experience following SOPs and executing batch records
Work Environment
The role involves working in both a lab and office setting. The lab is a cleanroom, classified as level 10k and 100k, requiring the analyst to perform sterile gowning and maintain certification for sterile gowning. The company is at the forefront of cellular therapy development, focusing on preserving kidney function and potentially delaying or eliminating the need for dialysis. The work environment is dynamic and innovative, contributing to transformative therapeutic solutions.
Pay and Benefits
The pay range for this position is $25.00 - $28.00/hr.
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 WINSTON SALEM,NC.
Application Deadline
This position is anticipated to close on Oct 1, 2025.
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 30,000 consultants and more than 4,500 clients across the U.S., Canada, Asia and Europe, Actalent serves many of the Fortune 500.
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 due to a disability, please email (% ) for other accommodation options.

Job Title: Quality Environmental Monitoring Specialist

Job Description

We are seeking a motivated Quality Environmental Monitoring Specialist to join our team. This role offers an exciting opportunity to be at the forefront of environmental monitoring within our main Readycare division. You will play a crucial part in ensuring the quality and safety of our medical device and pharmaceutical products. Room for growth within organization.

Responsibilities

• Perform environmental monitoring of cleanrooms and controlled areas, including viable air, non-viable particles, critical surface monitoring, and personnel monitoring.

• Collect routine environmental samples from surfaces, air, and water.

• Maintain accurate documentation of sampling information and results in compliance with Good Documentation Practices (GDP).

• Label environmental samples and submit them to the laboratory via LIMS.

• Submit finished good products for additional testing.

• Review and perform trending on environmental monitoring results.

• Assist with investigations related to out-of-specification (OOS) results, excursions, or contamination events.

• Adhere to internal quality procedures, including proper gowning, hygiene, and microbial control, to maintain cleanliness within cleanrooms.

• Assist in the development and implementation of processes, reports, data analysis, and procedures within the defined area of specialization.

• Perform audits to review all related documentation for completeness, accuracy, and ensure the product and reports meet all specifications.

Additional Skills & Qualifications

• High school graduate or GED required; Associate or Bachelor's degree in biology, microbiology, or a related field preferred.

• 0 to 2 years of work experience within a manufacturing environment, with GMP experience preferred.

• Attention to detail in sampling techniques, with experience in environmental monitoring and aseptic technique.

Pay and Benefits

The pay range for this position is $24.00 - $30.00/hr.

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 North Chicago,IL.

Application Deadline

This position is anticipated to close on Oct 22, 2025.

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 30,000 consultants and more than 4,500 clients across the U.S., Canada, Asia and Europe, Actalent serves many of the Fortune 500.

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 due to a disability, please email (% ) for other accommodation options.

Overview

We are seeking a dedicated and detail-oriented Quality Environmental Monitoring Specialist to join our team. This role is critical in ensuring the cleanliness and regulatory compliance of cleanrooms and controlled environments through rigorous environmental monitoring and documentation practices.

Responsibilities

• Conduct environmental monitoring of cleanrooms and controlled areas, including:
  • Viable air sampling
  • Non-viable particle counting
  • Critical surface monitoring
  • Personnel monitoring
• Collect routine environmental samples from surfaces, air, and water.
• Accurately document sampling data and results in accordance with Good Documentation Practices (GDP).
• Properly label and submit environmental samples to the laboratory using LIMS.
• Submit finished goods for additional testing as required.
• Review and analyze environmental monitoring data for trends.
• Support investigations related to:
  • Out-of-specification (OOS) results
  • Excursions
  • Contamination events
• Follow internal quality procedures for gowning, hygiene, and microbial control to maintain cleanroom integrity.
• Assist in developing and implementing processes, reports, data analysis, and procedures within the area of specialization.
• Perform audits to ensure documentation accuracy and product/report compliance with specifications.

Qualifications

• Required: High school diploma or GED
• Preferred: Associate or Bachelors degree in Biology, Microbiology, or a related scientific field
• Preferred: 02 years of experience in a manufacturing environment
• Preferred: Familiarity with Good Manufacturing Practices (GMP)

Pay and Benefits

The pay range for this position is $24.00 - $30.00/hr.

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.

• 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 Gurnee, IL.

Application Deadline

This position is anticipated to close on Sep 17, 2025.

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 30,000 consultants and more than 4,500 clients across the U.S., Canada, Asia and Europe, Actalent serves many of the Fortune 500. 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 due to a disability, please email actalentaccommodation@ for other accommodation options.

Seniority level

• Entry level

Employment type

• Full-time

Job function

• Quality Assurance

Industries

• Business Consulting and Services

#J-18808-Ljbffr

Environmental Monitoring (EM) Specialist

We are seeking a motivated and detail-oriented Environmental Monitoring (EM) Specialist to perform routine environmental sampling and support contamination control within our sterile pharmaceutical compounding cleanroom facilities. This role is essential in ensuring a controlled environment for aseptic operations and maintaining compliance with USP , USP , and 503A/503B regulatory standards.

Working under the supervision of the Microbiologist, the EM Specialist will be responsible for executing all aspects of the environmental monitoring program, including sample collection, incubation, documentation, reporting, and assisting in microbial investigations and laboratory submissions.

You Will:

• Perform routine non-viable and viable air sampling, surface sampling, and personnel monitoring sampling within ISO-classified cleanroom environments.
• Ensure proper handling and labeling of sampling media to maintain integrity throughout the sampling and incubation process.
• Accurately document sampling events, locations, results, and observations in compliance with internal SOPs and regulatory expectations.
• Adhere to defined sampling schedules and respond to unscheduled or investigative sampling needs.
• Manage the proper incubation of solid and liquid microbiological media at appropriate temperature conditions (e.g., 2025C and 3035C).
• Perform interim and final readings of incubated media plates to identify and enumerate Colony Forming Units (CFUs).
• Report and investigate results at alert and/or action levels.
• Support the Microbiologist in responding to microbial growth events, including sample handling, documentation of excursions, and generation of preliminary reports.
• Coordinate submission of microbial-positive samples to third-party laboratories and assist in investigation data gathering.
• Maintain investigation logs and contribute to root cause analysis and corrective action activities.

You Have:

• Minimum 1 year of experience in one or more of the following:
• Non-viable particulate air sampling
• Viable air sampling using impaction or settling plates
• Surface sampling using contact plates or swabs
• Personnel aseptic technique and gown sampling
• Knowledge in gram staining and microbial growth identification.
• Ability to work in sterile garb for extended periods within an ISO Class 5 or cleaner environment.
• Successful completion or ability to pass initial and ongoing garbing and aseptic competency evaluations.
• Working knowledge of USP , USP , USP , and sterile compounding requirements.

Preferred Qualifications:

• Licensed Pharmacy Technician with active state licensure and PTCB certification.
• Prior experience in a 503A or 503B compounding pharmacy or aseptic pharmaceutical manufacturing environment.
• Familiarity with microbial growth morphology and plate reading.
• Understanding of incubation practices, environmental excursion documentation, and laboratory sample chain-of-custody procedures.
• Strong attention to detail and commitment to aseptic technique and contamination control.

Our Benefits (there are more but here are some highlights):

• Competitive salary & equity compensation for full-time roles
• Unlimited PTO, company holidays, and quarterly mental health days
• Comprehensive health benefits including medical, dental & vision, and parental leave
• Employee Stock Purchase Program (ESPP)
• 401k benefits with employer matching contribution

Conditions of Employment:

• This position will require working with Hazardous Drugs (HD) and would require that Personal Protective Equipment (PPE) be worn for the length of working with these drugs. These items would include gloves, respiratory protection, gown and other items as required.
• This position requires medical approval to wear respiratory protection in the form of negative or positive pressure respirators, including N95, full face respirator, SCBA, or Powered Air Purifying Respirator (PAPR).
• Physical exertion required. Including, but not limited to, walking up to 50% of the time, standing up to 100% of the time, squatting and bending up to 20% of the time and lifting up to 80% of the time for up to a twelve hour shift. Must be able to lift up to 50lbs.
• Due to the risk of reproductive capability in handling or compounding certain Hazardous Drugs (HD) associates must be willing to confirm that they understand the potential risks (teratogenicity, carcinogenicity and reproductive effects) of handling hazardous drugs.

We are committed to building a workforce that reflects diverse perspectives and prioritizes ethics, wellness, and a strong sense of belonging. If you're excited about this role, we encourage you to applyeven if you're not sure if your background or experience is a perfect match.

Hims considers all qualified applicants for employment, including applicants with arrest or conviction records, in accordance with the San Francisco Fair Chance Ordinance, the Los Angeles County Fair Chance Ordinance, the California Fair Chance Act, and any similar state or local fair chance laws.

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.

Hims & Hers is committed to providing reasonable accommodations for qualified individuals with disabilities and disabled veterans in our job application procedures. If you need assistance or an accommodation due to a disability, please contact us at accommodations@ and describe the needed accommodation. Your privacy is important to us, and any information you share will only be used for the legitimate purpose of considering your request for accommodation. Hims & Hers gives consideration to all qualified applicants without regard to any protected status, including disability.

To learn more about how we collect, use, retain, and disclose Personal Information, please visit our Global Candidate Privacy Statement.