Quality Administrator Technician

Industry

Manufacturing and Production

Advert ID

USA_454504

Location

West Chester

Job Type

Contract

Hours

Full-Time

Salary Range

Up to USD21.49/hr

No. of Openings

1

Branch Information

Cincinnati, OH - N. Kentucky - (USA) 8743 Union Centre Boulevard OH West Chester , OH - 45069 Phone : 513-772-2220

ContactNumber

513-772-2220

Job Description

Manpower is now hiring for Quality Administrator Technician needed in the West Chester, Oh area. This position is not manufacturing focused, but more so quality focused. Particularly, Microbiology. Do you enjoy working in a fast-passed environment, with a job that offers overtime? Do you have knowledge of GMPs and FDA policies/procedures? If so, look no further- we have the job for you! Our client is a global Pharmaceutical Company who is innovative and growing who offers a competitive salary.

What's in it for you?

*Shift 6p-6a, 2-2-3 rotating Shift

*Competitive wages starting at $21.49/Hr

*Temporary to hire, based on performance

What is the job?

*Performs environmental monitoring and plate reads for the West Chester site.

*Wear sterile garments and PPE (Personal Protective Equipment) as required by specific activities.

*Operate sterilized systems and equipment utilizing aseptic technique, and/or in controlled aseptic Basic comprehension of standard processing in a manufacturing environment.

*Within required parameters conduct process checks to ensure that processes are operating.

*Ensure proper documentation practices during production including batch record and log entries as required.

*Participate in spill control, handling of hazardous materials, and first aid.

*May serve as the link between the PET team and QC Microbiology for day-to-day activities, such as schedules, sample submissions, and workload planning.

*Must have the ability to effectively understand, read, write, communicate and follow instructions in the English language.

*Ensure proper documentation practices during production including batch record and log entries as required.

*Attend team meetings to discuss progress, and/or continuous improvement initiatives.

*Read, understand, and comply with GMP (Good Manufacturing Practices) and SOPs (Standard

*Operating Procedures), including general safety, lock outs, etc.

What you bring to the job?

*High school graduate, vocational school graduate or equivalent

*3 Year of experience in a pharmaceutical or GMP regulated environment

*Must have the ability to effectively understand, read, write, communicate and follow instructions in the English language.

*Good attention to detail is required. Individual must be capable of keeping accurate records, performing mathematical calculations.

*Experience on GMP and FDA Policies and procedures.

*Sampling experience/any background related to lab/micro/EM sampling.



Preferred Background:

* Aseptic production experience.

* Advance education beyond high school in science-related field

* Experience working in a LEAN manufacturing environment

* Knowledge of GMPs and FDA policies/procedures

Stop your job search and apply today. Do you need more information?

Contact our Recruiter's today at 513-772-2220. Or email natalie.curd@manpower.com.

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