Environmental Monitoring Technician

Eurofins USA; North Brunswick Township (NJ); On-site; USD 50,000 - 70,000; Full time

Job summary

A leading company in life sciences is seeking an Environmental Monitoring Technician to perform testing and monitoring in GMP biopharmaceutical manufacturing. This role involves routine microbiological testing, operating specialized equipment, and ensuring compliance with safety standards. The ideal candidate will have 2+ years of experience in the biotech industry and a relevant degree. Excellent benefits and full-time hours offered.

Benefits

Comprehensive medical coverage

Dental and vision options

Life and disability insurance

401(k) with company match

Paid vacation and holidays

Qualifications

• 2+ years of biotech industry experience in GMP biopharmaceutical manufacturing.
• Ability to perform aseptic and microbiological techniques.

Responsibilities

• Perform environmental monitoring and routine microbiological testing.
• Operate monitoring equipment and document results.
• Assist in training new EM Laboratory Technicians.

Skills

Aseptic Techniques

Microbial Isolation

Judgment

Education

Bachelor's degree in Microbiology

Tools

Laser Particle Counter

Viable Air Sampler

Microscope

pH Meter

Job 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, identity, composition, authenticity, origin, traceability and purity of biological substances and products.

Job Description

About the job

This role is for an Environmental Monitoring Technician that will perform testing work at Client sites, including air travel (10-20%).

Your Role:

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, and pH meter.
• 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 won 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.
  

Preferred 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

Positions are full-time, workingTuesday-Saturday 8am-5pm,overtime as needed. Candidates currentlyliving within commutable distance to North Brunswick Township, NJare encouraged to apply.

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

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

What Happens Next

Our people are the backbone of what we do, so it's incredibly important we find the right individuals to join us. As a potential new recruit you'll be invited to meet the team in the form of an assessment centre or a staged interview process dependent on the role and it's requirements, this will give you the opportunity to see what working for Eurofins is really like and enable us to get you know your key skills and strengths.

Your data

As part of any recruitment process, the company collects and processes personal data relating to job applicants. The company is committed to being transparent about how it collects and uses that data and to meeting its data protection obligations.

Closing Date

We reserve the right to close or extend this position depending on application numbers. Therefore we would urge candidates to submit an application as early as possible.

Due to the high volume of applications we receive please be aware that if you do not receive a response within 4 weeks of the vacancy expiry date unfortunately, on this occasion your application has been unsuccessful.

Eurofins is aM/F, Disabled, and Veteran Equal Employment Opportunity and Affirmative Action employer.

Eurofins USA BioPharma Services is a M/F, Disabled, and Veteran Equal Employment Opportunity and Affirmative Action employer.