Manufacturing Technician 5.0 5.0 out of 5 stars Houston, TX 77047 Manufacturing Technician SRG offers flexible staffing solutions with a national presence. We provide contract, contract-to-hire, direct hire and executive search services. SRG utilizes an innovative approach to identify and qualify talent that is unique to the Staffing industry, featuring a cutting-edge platform that allows us to rapidly and precisely match professionals to client requirements. We have a proprietary database of over one million candidates and maintain continuous contact with our qualified talent.

Title:

Manufacturing Technician -

Environmental Monitoring Location:

Houston, TX Industry:

Pharmaceutical Hours:

7am-7pm, 12 hour rotating shifts - 2 days on, 2 days off, 3 days on, 3 days off

Salary:

$26.80/ hr. Paid Weekly (Benefits are Available)

Employment Type:

Contract (long term with direct hire consideration)

Environment:

A global leader and trusted supplier in the pharma, biotech and specialty ingredients markets. The company is focused on advanced manufacturing, high-quality control systems, regulatory expertise, and research and development (R D) capabilities. The company s products and services include active pharmaceutical ingredients (API), stem cell therapies, drinking water sanitizers, vitamin B compounds, organic personal care ingredients, industrial preservatives and microbial control solution to combat viruses, bacteria and other dangerous pathogens.

Job Summary:

The Environmental Monitoring (EM) Manufacturing Technician will be responsible for conducting EM tasks in support of production and aseptic processing of clinical grade products. The core tech will also be responsible for maintaining, stocking, and set-up of clean room environment.

Job Duties:

Participates in the Environmental Monitoring process as part of GMP production of viral therapies Cell culture and product purification using aseptic technique when required Coordinates EM equipment needs with QC EM team for Manufacturing processes Drafting, completion and revision of manufacturing documents including Batch Records and EM forms Buffer and component preparation including operation of steam autoclave Operation of manual, semi-automated and automated equipment in support of routine clinical production Operating Environmental monitoring equipment such as Solairs, ApexZ50, active counters Requirements Bachelor's Degree in Life Sciences preferred. Basic Lab experience with a Bachelor's degree or Intermediate Lab experience within a cGMP clinical production environment and a High School Diploma. Experience within pharmaceutical, cell/gene, therapy, biologics is preferred

ADA/EOE IND123

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