Job Title: Environmental Monitoring Analyst II Job Description Our client, a global bio-pharmaceutical company specializing in generic sterile injectable manufacturing, is seeking motivated individuals to join their Environmental Monitoring Team. The Environmental Monitoring Analyst II will be responsible for viable and non-viable monitoring of the manufacturing areas, including air, water, and surface sampling. Samples will be logged in a proprietary LIMS, and cGMP documentation practices will be adhered to. Analysts will also be responsible for processing water, product, and commodity samples and performing bioburden testing. This role also involves training new hires, integrating them into the pharmaceutical industry, and participating in process improvement initiatives.
Responsibilities - Conduct viable and non-viable monitoring of manufacturing areas, including air, water, and surface sampling.
- Log samples in a proprietary LIMS and adhere to cGMP documentation practices.
- Process water, product, and commodity samples and perform bioburden testing.
- Assist supervisors in training new hires and integrating them into the team.
- Act as an interim lead for supervisors as needed.
- Participate in process improvement initiatives.
- Perform bioburden testing on water and pharmaceutical product samples.
- Test commodities for non-viable or viable particulates.
Essential Skills - Bachelor's degree in Microbiology, Biology, or related life science field with 1+ years of pharmaceutical industry experience in environmental monitoring.
- Associates degree or HS diploma with 3-4 years of environmental monitoring experience in the pharmaceutical industry.
- Experience with aseptic gowning and sampling in an aseptic manufacturing environment.
- Proficiency in LIMS and MODA systems.
Additional Skills & Qualifications - Experience with pharmaceutical lab setup, cGMP manufacturing, clean room practices, aseptic lab processing, and bioburden testing.
- Strong leadership and training skills.
- Flexibility with schedule changes and ability to work in a fast-paced environment.
Work Environment This position involves working in a pharmaceutical manufacturing environment, with approximately 80% of the time spent in manufacturing areas and 20% in the lab. The work schedule includes a 2,2,3 rotating shift, with options for day (7am-7pm) or night (7pm-7am) shifts. The EM team comprises 45-50 people split across day and night shifts, working in Grade A, B, C, D areas. Gowning is required, and individuals must be comfortable with tight spaces and adhere to strict dress codes (no makeup, fake nails, or jewelry). Training involves a few months of working with specific team trainers to become certified in routine job tasks.
Pay and Benefits The pay range for this position is $27.00 - $32.00/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 Raleigh,NC.
Application Deadline This position is anticipated to close on Feb 24, 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.
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