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Environmental Monitoring Technician I

Industry

Pharmaceuticals

Advert ID

USA_391682

Location

Durham

Job Type

Contract

Hours

Full-Time

Salary Range

No. of Openings

1

Branch Information

Raleigh - Durham NC Area - (USA) 430 Davis Drive Suite 100 NC Morrisville , NC - 27560 Phone : 855-591-7454

ContactNumber

855-591-7454

Job Description

Do you have experience in Environmental Monitoring, Aseptic Manufacturing, or Microbiological Laboratory Operations? Are you looking for your next big career opportunity? We may have exactly what you are looking for! A leading global biopharmaceutical company is looking for an Environmental Monitoring Technician in Durham, NC!



Specific to Environmental and Utility Monitoring, the Analyst will be responsible for maintaining the EM program to include the following:

*Collection and testing of qualified Utility systems including Clean Steam, WFI and compressed gases

*Execute environmental sampling of Classified Areas including active air sampling, surface sampling and non-viable air sampling

*Provide data entry, review and approval as required

*Provide summaries of test results to appropriate personnel as needed

*Compile and evaluate environmental data for adverse trends

*Directly support Performance Qualification activities

*Perform routine monitoring of Personnel

*Compile and author Annual Reviews

*Author and summarize Requalification, Performance Qualification, and Special Study protocols.

*Perform monthly and weekly sample accountability

*Submit LIMS sample rejections

*Equipment Calibration and Management

*Filing data sheets and document control of logbooks

*Other duties requested by Management



Qualifications

*At least 1-3 years of relevant post-degree work experience in Environmental Monitoring, Aseptic Manufacturing or Microbiological Laboratory Operations

*Evidence of good oral and written communication skills, i.e. effective presentation of concepts and ideas, as well as interpersonal and conflict resolution skills

*Attention to detail, flexibility and an awareness of production and attendant quality control problems

*Basic understanding of GMPs and of regulatory requirements as they apply to the vaccine, sterile pharmaceutical or related fields

*Ability to sit, stand and move within work space for extended periods, ability to perform repetitive tasks including frequent hand to finger manipulations, grasping pushing and pulling; ability to lift up to 50 pounds

* Qualifications Preferred: Quality Control, Quality Assurance and/or cGMP experience



Schedule: Tuesday-Saturday, 2:30 p.m.-1:00 a.m.

Duration: 1 year contract