JobWatch

16 days old

Quality Document Control Specialist - Nutraceutical, Anaheim, CA

Kelly Services
Anaheim, CA 92805
**Quality Document Control Specialist** **-** Nutraceutical, Anaheim, CA



**Job Duties and Responsibilities:**




+ Manages and process DCRs, & SOPs. Track revision history.

+ Reviews documentation to assure accuracy and completeness.

+ Maintains files and data archiving of controlled QA documents.

+ Maintains documents in accordance with department SOPs. Analyzes all documents to ensure that controls regarding format and content are incorporated.

+ Maintains database of information including all document numbers, dates and distribution requirements. Generates logs, indexes and distribution lists as required. Assures that all documents are reviewed for continuing compliance to cGMPs and company policies on a periodic basis.

+ Processes change control activities includes assigning tracking numbers, routing, tracking, and expediting change control packages, distributing new documents and retrieving obsolete ones, performing changes to text documents, and reporting on change control status to management.

+ Maintains Quality documents, including, but not limited to, Reports, COA, Batch Records, training, test methods, forms and other supporting documents.

+ Issues, but not limited to, batch records, logs, forms and other documents as requested or as scheduled.

+ Tracks the issuance of deviations, CAPAs, NCMRs, OOS, Complaints

+ Coordinates in-house training for new and revised documents as required. Maintains hard-copies and electronic database of all employee training records.

+ Recommends corrective actions for quality issues.

+ Ensures daily work flow completion.

+ Assist on timely release of finished goods.

+ Assign control number to change requests.

+ Assist in the monitoring and record keeping of pest control activities.

+ Assist in the validation and verification efforts.

+ Coordinates destruction of expired products and records.

+ Assist in preparation for customer audits and regulatory inspections.



**Job Requirements:**




+ Knowledge of 21 CFR part 111

+ Knowledge of G.F.SI. certifying bodies such as N.S.F., Organic Certifications, etc)

+ 2+ years operating in Quality in a cGMP manufacturing environment, preferably under 21 CFR 111.

+ Proficient in Microsoft Word & Excel

+ Proficient in GDPs including reviewing Batch Record Documentation for Compliance.

+ Familiarity with reviewing test results

+ Maintaining files according to SOPs and applicable agency compliance.

+ Maintaining, reviewing, and Filing cGMP documentation

+ Batch Production and Packaging records

+ Standard Operating Procedures(SOP)

+ technical reports

+ Logs

+ Calibration records

+ Experience with Standard Operation Procedures

+ Degree preferred but not required, experience is preferable



**If you meet the above qualifications, please submit your resume for immediate consideration. Questions? Call Airika at 562-206-2707**



**To schedule a time to connect, please click the link to add your availability to my calendar** . https://calendly.com/airc843/30min?month=2020-09




**Why Kelly** **** **?**



Kelly Science & Clinical is your connection to premier scientific and clinical companies looking to hire talented people just like you. Every day, we match science professionals with dream jobs that fit their skills and interestsits the way we think job searching should be. Nearly 100 percent of our science recruiters have a professional background/education in science, so we know a thing or two about the science market and how to get you noticed.




**About Kelly** ****



At Kelly, were always thinking about whats next and advising job seekers on new ways of working to reach their full potential. In fact, were a leading advocate for temporary/non-traditional workstyles, because we believe they allow flexibility and tremendous growth opportunities that enable a better way to work and live. Connecting great people with great companies is what we do best, and our employment opportunities span a wide variety of workstyles, skill levels, and industries around the world.


Kelly is an equal opportunity employer committed to employing a diverse workforce and providing accommodations for people with disabilities in all parts of the hiring process as required under its Employment Accommodation Policy. Kelly will work with applicants to meet accommodation needs that are made known to Kelly in advance.

Categories

Posted: 2020-10-14 Expires: 2020-11-14

Before you go...

Our free job seeker tools include alerts for new jobs, saving your favorites, optimized job matching, and more! Just enter your email below.

Share this job:

Quality Document Control Specialist - Nutraceutical, Anaheim, CA

Kelly Services
Anaheim, CA 92805

Join us to start saving your Favorite Jobs!

Sign In Create Account
Powered ByCareerCast