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Document Control Specialist

Kelly Services

Dallas, TX
Job Code:
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Job Details

Job Title Document Control Specialist

Jobid US589HKR_BH1420096

Location: Dallas, TX, 75219, USA

Description **_Quality Assurance /Document Control – Nutraceutical Industry!_**

Kelly Scientific Resources is currently seeking a QA/Document Control Specialist for one of our top manufacturing clients in Dallas, TX.

As a QA/Document Control Specialist placed with Kelly Scientific Resources, you will facilitate the flow of information through the company and ensures quality of information. Actively seeks to increase the value of information by making it readily available, usable, and actionable. Regulates the control, distribution, retention, and archiving of cGMP documents. Ensures documentation is compliant with internal procedures as well as regulatory and statutory standards. Works under the general supervision of the Director of Quality.

**Additional Job Responsibilities:**

+ Writes, updates, issues, and maintains QA documentation including, but not limited to, SOPs, Work Instructions, Forms, Technical Files, Master Manufacturing Records, Batch Records, Specifications, and other GMP related documents.
+ Develops new processes and improvements on existing quality processes.
+ Works to improve the quality of processes by gathering data and applying problem solving techniques.
+ Coordinates the change control process.
+ Coordinates periodic review of all SOPs.
+ Identifies areas in need of process improvement in regards to efficiency and/or quality and makes changes following approved change control procedures.
+ Works collaboratively with subject matter experts as needed for SOP development.
+ Assists Quality Management in establishing, implementing and maintaining the quality management system.
+ Creates, updates, and maintains Master Manufacturing Records (MMRs) and Master Packaging Records (MPRs)
+ Functions as document control software administrator including controlling content type, document control numbers, user rights, and user groups
+ Reviews all new and revised controlled documentation for appropriate format, content, and consistency with other documentation.
+ Assists in implementation of improved document management systems.
**Education/Job Requirements:**

+ Bachelor’s degree in related field
+ 1-3 years experience working in a manufacturing environment as a Quality Assurance or Document Control
+ Technical writing experience, including process writing and document design
+ Excellent computer skills in Microsoft Suite.
+ Familiarity with Visio a plus.
+ Familiarity with Ensur a plus
+ Presentation Skills
+ Good writing, grammar and communication skills
+ Temp-to-Hire
+ $20-25 per hour/1st Shift
**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 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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