282 Environmental Monitoring jobs in the United States

Our client, a world-renowned research institution, is seeking an Environmental Monitoring Technician to join their team on a contract basis.

Type: Contract

Location: Los Angeles County, CA

Rate: $25 - $33/hr

• Operate various equipment within GMP-regulated environments to support production and quality operations.
• Accurately document all activities, procedures, and outcomes in accordance with established protocols.
• Follow and enforce proper documentation standards throughout all job functions.
• Read, understand, and execute Standard Operating Procedures (SOPs) as required.
• Maintain detailed and accurate records, including laboratory notebooks, quality logs, and sample tracking.
• Complete all mandatory training programs to ensure compliance and proficiency.
• Assist and guide team members on SOPs, control documents, and other relevant work instructions.
• Coordinate with support teams to ensure smooth operational workflow.
• Conduct routine audits of SOPs and work instructions to maintain adherence to regulatory standards.
• Perform scheduled environmental or process sampling and input associated data accurately.
• Adhere to gowning protocols by wearing sterile garments and personal protective equipment (PPE) as dictated by specific tasks.
• Interpret technical diagrams, drawings, and schematics relevant to the work environment.
• Identify and recommend corrective actions to ensure equipment and work areas remain compliant with regulatory requirements.

Bachelors Degree in Life Sciences. One to two years of experience in a pharmaceutical production environment. Knowledge of cGMPs and FDA policies / procedures.

This job description is a complete list of all desired skills, but not all are required. We strongly encourage candidates who have some of the skills to apply. We look forward to a conversation to learn more about you!

We are an equal opportunity employer and all qualified applicants will receive consideration for employment without regard to race, color, religion, sex, national origin, disability status, protected veteran status, or any other characteristic protected by law.

Environmental Monitoring and Sampling Perform sampling of air for viable and non-viable particle counts along with contact surface testing Perform sampling and testing of facility gasses and facility water Manage the incubation of samples, plate reading and reporting of resultsDocumentation and Safety Ensure required testing documentation is complete and generated with adherence with GMP and to company policies and procedures Escalate to management any failures and concerns related to environment of controlled spaces Assist in sustaining of the laboratory safety and cleanliness by maintaining inventory, disposal of waste and routine cleaning of laboratory rooms and equipment Assist in receipt and log in of in-process samplesOverall Microbiology support Attend support meetings (as required)Perform additional duties as required and assigned by managementWe are a company committed to creating diverse and inclusive environments where people can bring their full, authentic selves to work every day. We are an equal opportunity/affirmative action employer that believes everyone matters. Qualified candidates will receive consideration for employment regardless of their race, color, ethnicity, religion, sex (including pregnancy), sexual orientation, gender identity and expression, marital status, national origin, ancestry, genetic factors, age, disability, protected veteran status, military or uniformed service member status, or any other status or characteristic protected by applicable laws, regulations, and ordinances. If you need assistance and/or a reasonable accommodation due to a disability during the application or recruiting process, please send a request to com. To learn more about how we collect, keep, and process your private information, please review Insight Global's Workforce Privacy Policy: . some environmental monitoring experience would be a plus! -GMP experience with strong GDP understanding -some experience gowning into clean rooms (grade C/D)

• Perform routine and investigational environmental monitoring of classified
• manufacturing, filling, and support areas, as well as operations personnel monitoring.
• Support daily EM laboratory operations.
• Key Objectives/Deliverables:
• Support production operations by means of EM sampling of classified manufacturing, filling, and support areas and operations personnel.
• Support daily EM laboratory operations and process/equipment qualification activities as necessary
• Ensures compliance with current Good Manufacturing Practices (cGMPs) and maintain constant inspection readiness.
• Ensures that data integrity is maintained
• Participate in process streamlining and continuous performance improvement.
• Responsible for maintaining a safe work environment, working safely and accountable for supporting all HSE Corporate and Site Goals.

• High School Diploma or equivalent.

• Strong understanding of cGMPs.
• Understanding of regulatory standards / requirements for EM.
• Knowledge of / familiarity with Parenteral production environments and operations.
• Strong computer skills, documentation skills and attention to detail.
• Responsible for maintaining a safe work environment, working safely and accountable for supporting all HSE Corporate and Site Goals.
• Environmental Monitoring experience preferred.
• Manufacturing or production experience preferred.
• Experience in Aseptic manufacturing or production, QC, QA, Technical Services, or Regulatory is desirable.
• Technical writing and written communication skills are a plus.

• Known allergens in area.
• Work in a dynamic and fast paced environment with potential to work shifts and weekends.
• Must be able to lift 30 pounds and be able to pass, push, and pull to execute specific aspects of job duty.
• Post Offer testing exam may be required.
• Overtime may be required.
• EM Technician tasks involve repetitive motions.
• EM Technician requires gowning certification, and repeatedly aseptically gown on a daily basis.
• Must be able to stand / walk for extended periods of time.
• Weekend overtime routinely occurs based on a rotating schedule.

Job DescriptionJob DescriptionCompany Description

Eurofins Scientific is an international life sciences company, providing a unique range of analytical testing services to clients across multiple industries, to make life and our environment safer, healthier and more sustainable. From the food you eat, to the water you drink, to the medicines you rely on, Eurofins laboratories work with the biggest companies in the world to ensure the products they supply are safe, their ingredients are authentic and labelling is accurate.

The Eurofins network of companies is the global leader in food, environment, pharmaceutical and cosmetic product testing and in agroscience Contract Research Organization services. It is one of the market leaders in certain testing and laboratory services for genomics, discovery pharmacology, forensics, advanced material sciences and in the support of clinical studies, as well as having an emerging global presence in Contract Development and Manufacturing Organizations. It also has a rapidly developing presence in highly specialized and molecular clinical diagnostic testing and in-vitro diagnostic products.

In over 30 years, Eurofins has grown from one laboratory in Nantes, France to 58,000 staff across a decentralized and entrepreneurial network of 900 laboratories in over 54 countries. Eurofins companies offer a portfolio of over 200,000 analytical methods to evaluate the safety, , composition, authenticity, , traceability and purity of biological substances and products.

Job Description

The Environmental Monitoring Technician performs environmental monitoring and routine microbiological testing within a GMP biopharmaceutical manufacturing organization.

•    Performs routine and non-routine Environmental Monitoring (EM) such as water sampling, non-viable particulates, viable air, viable surfaces, and gas testing in cleanroom environments within the Manufacturing area at Client’s site, as per applicable standard operating procedures (SOP).
•    Perform environmental monitoring for aseptic filling processes according to SOP.
•    Operate monitoring equipment that includes but is not limited to Laser Particle Counter, Viable Air Sampler, Microscope, MilliFlex OasisTest System, Conductivity meter, pH meter and TOC analyzer.
•    Read EM (Environmental Monitoring) data and document results on relevant forms.
•    Perform trending and generate trending charts for EM data.
•    Participate in validation/verification of controlled environments such as cleanroom, and gowning qualification.
•    Perform Quality Control testing such as media and organism qualification as per applicable procedures.
•    Assist in USP standard testing including but not limited to water sampling, incubation of samples, and enumeration.
•    In cooperation with the Laboratory Manager, responsible for the preventative maintenance of critical EM equipment.
•    Monitor test status and conditions as described in Work Instructions and SOPs.
•    Record test results accurately and legibly on all documents.
•    Technical report writing including text, tables, graphs, and diagrams.
•    Report any deviations and/or nonconformities to Management as well as provide possible preventive and corrective measures to prevent future deviations and non-conformities.
•    Assist with OOS, NI, CAPA, and Change Control processes in response to Laboratory issues.
•    Follow and perform process qualifications and validations for procedures and/or equipment.
•    Update procedures for improvement to methods.
•    Able to lift at least 50 lbs.
•    Assist in the training of new EM Laboratory Technicians.
•    Perform bioburden testing of samples per USP, EP requirements.
•    Perform Area Release per protocol for campaigned manufacturing areas.
•    Comply with all safety policies, practices, and procedures.
•    Participate in proactive team efforts to achieve departmental and company goals.
•    Driving a company car for offsite work
•    Perform other duties as assigned.

Qualifications

Minimum Qualifications:

• 2+ years of biotech industry experience within a GMP biopharmaceutical manufacturing organization.
• Licensed driver with good driving record
• Ability to apply knowledge of good manufacturing practices and good laboratory practices daily.
• The understanding and ability to perform aseptic and relevant microbiological techniques such as microbial isolation, streak plate and gram staining.
• Ability to follow gowning practices for cleanroom environments.
• Ability to exercise judgment within defined procedures and practices to determine appropriate action.
   

Qualifications:

• Bachelor’s degree (B.A.) or equivalent from four-year college or university, preferably in Microbiology or a relevant life sciences discipline.
• 2+ years of related experience and/or training; or equivalent combination of education and experience.
• 2+ years of industry experience working with mammalian cell culture.

Additional Information

Position is full-time, working Monday-Friday 8am-5pm, overtime as needed.  Candidates currently living within commutable distance to San Diego, CA  are encouraged to apply.

Compensation Range: $25.48/hr - $30.00/hr 

Excellent full-time benefits including comprehensive medical coverage, dental, and vision options.

• Life and insurance
• 401(k) with company match
• Paid vacation and holidays

Eurofins USA BioPharma Services is a Disabled and Veteran Equal Employment Opportunity employer.

• Conduct viable and nonviable environmental monitoring throughout facility, including aseptic processing areas and classified manufacturing areas (Compounding, Component Preparation, Vial Wash, and Dispensary)
• Collect facility waters and submit for testing and accurately record results of above testing and promptly report any discrepancies or out of limit conditions to supervisor
• Perform Aseptic Gowning Training and certification sampling
• Requisition of materials, maintaining inventory and receive and store prepared media
• Prepare environmental monitoring plates and EM test reports for aseptic processing area
• Perform disinfection of incubator rooms weekly
• Follow safety requirements and maintains good housekeeping of laboratory area
• Incubate and inspect media fill units and incubate and examine samples for microbial growth
• Enumerate bacteria and report excursions
• Temperature charts for incubators and refrigerators in the Microbiology Laboratory
• Ensure processes and products are in compliance with all local, state, and federal rules and regulations. Oversee that processes are in cGMP compliance and establish systems that identifies opportunities for improvement and makes constructive suggestions for change to improve process effectiveness to heighten quality. Develop knowledge of and understand regulatory requirements such as 21CFR Parts 210 and 211, cGMP's, FDA, OSHA and other regulatory agencies.
• Assume additional duties and responsibilities as assigned

• Bachelor's degree in Chemistry, Microbiology, Biology or other related Science from an accredited university
• May consider an Associate's degree from an accredited university with minimum 3 (three) years of experience in the pharmaceutical industry (cGMP environment) and aseptic technique
• May consider a High School Diploma with minimum 5 (five) years of experience in the pharmaceutical industry (cGMP environment) and aseptic technique
• Minimum 1 (one) year's experience in the pharmaceutical industry (cGMP environment) and aseptic technique
• Ability to get gowning certified within 30 days
• Physical Requirements include - standing and walking up to 8 hours (4 hours at a time for aseptic processing area), lifting or moving up to 35 pounds and reaching with hands and arms up to 6 hours. Must be able to climb or balance, stoop, kneel, crouch, or crawl up to 1 hour.
• Must be flexible for working across shifts (nights and/or weekends) as needed

• A 'See it, Own it, Make it Happen' attitude.
• Excellent problem solving and critical thinking skills.
• Strong attention to detail and ability to follow standard procedures.
• Team collaboration and professional behaviors to align with Indivior guiding principles and core values.
• Good interpersonal and communication skills

• 3 weeks' vacation plus floating holidays and sick leave

• 401(k) and Profit Sharing Plan- Company match of 75% on your first 6% of contributions and profit sharing contribution equal to 4% of your eligible pay

• U.S. Employee Stock Purchase Plan- 15% Discount

• Comprehensive Medical, Dental, Vision, Life and Disability coverage

• Health, Dependent Care and Limited Purpose Flex Spending and HSA options

• Adoption assistance

• Tuition reimbursement

• Concierge/personal assistance services

• Voluntary benefits including Legal, Pet Insurance and Critical Illness coverage

• Gym, fitness facility and cell phone discounts

• Have unquestionable ethics and integrity with the willingness to stand firm on these principles even under significant pressure

• Risk IQ: Know what policies apply to your role and function and adhere to them.

• Speak Up: If you see something, say something.

• Have unquestionable ethics and integrity with the willingness to stand firm on these principles even under significant pressure

• Reinforce risk awareness with your team, with accountability and oversight for ongoing review and mitigation.

• Model and reinforce a Speak Up culture on your team.