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Environmental Specialist

ZipRecruiter, Durham

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Job Descriptionn

Client: Large Pharmaceutical Manufacturing Partner

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Where: RTP, Durham

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Title: Environmental Monitoring Technician

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Type: 6-12 month contract w/ extensions

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Schedule: 12 hour shift, 2-2-3 (2 days on, 2 days off, 3 days on, etc.). Contractors will work 36 hours one week, 48 the next, etc.

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Shift: Day and Night available

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Years Experience: 1+

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Benefits: Health, Dental, Vision, PTO, Sick days

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Expected Compensation: $27- 30/hr

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Summary:

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The QC Environmental Monitoring Technician will perform routine and investigational environmentalmonitoring of classified manufacturing, filling, and support areas. Support daily EM laboratory operations.

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Responsibilities:

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  • Support production operations by means of EM sampling of classified manufacturing, filling, and support areas and operations personnel.
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  • Support daily EM laboratory operations and process/equipment qualification activities, as necessary.
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  • Ensures compliance with current Good Manufacturing Practice (cGMP) and maintain constant inspection-readiness.
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  • Ensures that data-integrity is maintained
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  • Participate in process streamlining and continuous performance improvement.
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  • Responsible for maintaining a safe work environment, working safely and accountable for supporting all HSE Corporate and Site Goals.
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  • EM Technician requires gowning certification, and repeatedly aseptically gown daily.
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Requirements:

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  • High School Diploma or equivalent, Associates degree .
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  • Understanding of cGMP
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  • Excellent written and oral communication skills and ability to collaborate and interact with a team.
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  • Work in a dynamic and fast paced environment with potential to work shifts and weekends.
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  • Must be able to lift 30 pounds and be able to pass, push, and pull to execute specific aspects of job duty.
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  • Must be able to stand / walk for extended periods of time.
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Qualifications:

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  • Environmental Monitoring experience .
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  • Manufacturing or production experience .
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  • Experience in Aseptic manufacturing or production, QC, QA, Technical Services, or Regulatory is desirable.
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  • Technical writing and written communication skills are a plus.
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  • Understanding of regulatory standards / requirements for EM.
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  • Knowledge of / familiarity with Parenteral production environments and operations.
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  • Strong computer skills, documentation skills, and attention to detail.
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  • Responsible for maintaining a safe work environment, working safely, and accountable for supporting all HSE Corporate and Site Goals.
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  • Ability to focus on continuous improvement.
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  • Previous experience with laboratory IT systems including LIMS, LES, and standalone COTS systems.
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  • Understanding of compliance requirements and regulatory expectations for lab systems.
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Additional Information:

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  • Minimal travel required.
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  • Some allergens are present in the parenteral plant.
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  • 12 hour shifts on 2-2-3 schedule, days or nights
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