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Quality Control Analyst I

Kelly Services


Location:
Los Angeles, CA
Date:
04/19/2018
2018-04-192018-05-19
Job Code:
US41L7BS_BH1434323
Categories:
  • Healthcare
  • Monitoring
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Job Details

Job Title Quality Control Analyst I

Jobid US41L7BS_BH1434323

Location: Los Angeles, CA, 90006, USA

Description Kelly Services® has been providing outstanding employment opportunities to the most talented individuals in the marketplace. We are proud to offer a long-term temporary opportunity to work as a **Quality Associate** at a prestigious Fortune 500® company working in **Los Angeles, CA**

**Important information:** This position is recruited for by a remote Kelly office, not your local Kelly branch. To be considered for this position, you must use the “Submit Resume” button to submit your resumes. If you have questions about the position, you may contact the recruiter for this position ( Brooke.Schoen@kellyservices.com ) however your resume must be received via the “Submit Resume” button included within.

**Job Title: Quality Associate**

**Pay: $25 + depending on experience**

**Summary** :
Conduct specific biological, chemical and physical analyses on pharmaceutical products (biologics and drugs) and medical devices through all stages of the manufacturing process from incoming raw materials to finished goods, and may include environmental monitoring programs.

**Essential Duties and Responsibilities** :


+ Conduct critical biological, chemical and physical analyses such as raw materials, initial, in-process and final products, and samples collected from environmental monitoring programs at manufacturing facilities, etc.
+ Use a variety of laboratory instrumentation and computer systems to collect and record data (such as LIMS system). Perform assays requiring precise analytical skills and understanding of biology and chemistry principles.
+ Complete all testing, including special project / protocol testing in a timely and appropriate manner.
+ Maintain data integrity and ensure compliance with company SOPs and specifications, FDA, GLP, QSR and cGMP regulations.
+ Write exception documents.
+ Participate in functional efforts involving teams, which impact production, increase efficiency, solve problems, generate cost savings and improve quality.
+ Perform laboratory and manufacturing audits as required. Audit and update, as required, plant SOPs.
+ May perform equipment maintenance and calibrations as required. May perform other duties as assigned.
**Qualifications** :


+ Ability to handle multiple tasks concurrently, and in a timely fashion.
+ Computer literate. Must be detail oriented, conscientious and have high reading comprehension skills.
+ Must have basic understanding of laboratory instrumentation.
+ Must be able to communicate effectively with supervisors and peers.
+ Must be able to read, write, and converse in English.
+ Must be able to navigate, conduct searches, and fill on line forms on Personal Computer for the purposes of training, performance management, and self service applications.
+ Must have the ability to navigate electronic mail systems and intranet for communication purposes.
+ Good interpersonal skills and be able to work effectively and efficiently in a team environment.
+ Knowledge of cGMP manufacturing.
+ Knowledge of basic laboratory and pharmaceutical production equipment including but not limited to: autoclaves, process tanks, incubators, analytical equipment, and CIP/SIP systems.
+ Knowledge of basic chemical and biological safety procedures.
+ Must be able to read and follow detailed written instructions and have good verbal/written communication skills.
+ Must have the following personal attributes: integrity and trust, work ethic, sound judgment, intellectual honesty, pragmatism, courage and conviction.
+ Must have passion to innovate and drive for solutions.
+ Must display personal accountability for results and integrity.
+ Must display eagerness to learn and continuously improve.
+ Must have uncompromising dedication to quality
**Education and/or Experience** :

Bachelor’s Degree in Chemistry, or Biological Sciences with Analytical Chemistry or Laboratory coursework with 0-2 years’ experience. Appropriate additional certifications may be required pursuant to state or federal regulatory requirements

**We invite you to bookmark our Web site and encourage you to review it regularly for new opportunities worldwide:** www.kellyservices.com at http://www.kellyservices.com/ **.**

**_Kelly Services® is a U.S.-based Fortune 500 company. With our global network of branch locations, we are uniquely positioned to provide our customers with international staffing support and our employees with diverse assignments around the world._**

**Kelly Services is an Equal Opportunity Employer**

**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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