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QC Associate, Microbiology

Kelly Services


Location:
Union City, GA
Date:
04/19/2018
2018-04-192018-05-19
Job Code:
US589HAC_BH1428175
Categories:
  • Healthcare
  • Monitoring
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Job Details

Job Title QC Associate, Microbiology

Jobid US589HAC_BH1428175

Location: Union City, GA, 30291, USA

Description QC Associate, Microbiology

starting In April through December

**Overview**

The TEMP Quality Control Associate is responsible for performing daily lab operations with the assigned functional area related to the release of product, and/or monitoring of the IMF environment, as well as complete other assigned duties.

**Responsibilities**


+ Performs routine environmental monitoring, including air viable, particulate, viable surface sampling, and purified water system sampling/testing.
+ Performs assays for qualifying raw materials and for release or stability testing of in-process and finished products. These test methods may include flow cytometry, ELISA, endotoxin, complete blood count, viability, gram stain, growth promotion, and sterility.
+ Receives and maintains traceability and integrity of test samples, reagents and materials used in the laboratory per approved procedures.
+ Initiates and takes ownership as needed of laboratory investigations and exception reports for out-of-limit samples, and of other projects and related assignments.
+ Performs routine laboratory equipment maintenance.
+ Revises and updates standard operating procedures.
+ Performs testing in support of method validation studies.
+ Adheres to good documentation practices to ensure data integrity and traceability
+ Ability to work 12 hours shifts.
+ Ability to be flexible and support all functions by readily responding to changing circumstances (i.e.shift changes) and business needs.
**Qualifications**


+ Associate or Bachelor’s (preferred) degree in a scientific discipline or equivalent.
+ Typically 2+ years related experience in cGMP/FDA regulated industry.
+ Knowledge of basic lab testing techniques.
+ Basic level of analysis skills required to evaluate and interpret data to arrive at logical conclusions.
+ Attention to detail, quality and compliance with strict adherence to test procedures and protocols.
+ Ability to learn new technologies and processes quickly and to understand the technical concepts behind each assay performed.
+ Knowledge of cGMP/QSR/ICH and FDA device/drug/biologics regulations preferred.
+ Proficient in MS Office applications.
**Why Kelly** **®** **?**


With Kelly, you’ll have access to some of the world’s highest-regarded scientific organizations—providing you with opportunities to work on today’s most challenging, research-intensive, and relevantprojects. Our connections can lead you to innovative scientific pursuits you’ll be proud to helpadvance. We work with 95 of the Fortune 100™ companies, and found opportunities for more than 9,000scientific professionals last year.

You pursued a career in science to fuel your quest for knowledge and your desire to make the worlda better place. Let Kelly fuel your career—connect with us today.

**AboutKelly Services** **®**

As a workforce advocate for over 70 years, we are proud to directly employ nearly 500,000 people around the world and have a role in connecting thousands more with work through our global network of talent suppliers and partners. Revenue in 2017 was $5.4 billion. Visit kellyservices.com and connectwith us on Facebook , LinkedIn and Twitter .

Kelly Services is an equal opportunity employer including, but not limited to, Minorities, Females,Individuals with Disabilities, Protected Veterans, Sexual Orientation, Gender Identity and iscommitted to employing a diverse workforce. Equal Employment Opportunityis The Law.



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