This job was posted by https://www.vermontjoblink.com : For moreinformation, please see: https://www.vermontjoblink.com/jobs/1118101Perrigo\\\

　　Batch Record Auditor - Days\

　　Location:

　　Georgia, VT, US, 05468

　　\

　　Perrigo Company is dedicated to making lives better by bringing Quality,Affordable Self-care products that consumers trust everywhere they aresold. Help us do it.

　　\External applicants please note: To apply to this position please clickthe APPLY button at the bottom of the application. (The SAVE buttonwill only save your profile information but not submit an applicationfor this open position.) Thank you.

　　Description OverviewPerrigo Company is dedicated to making lives better by bringing highquality and affordable self-care products that consumers trusteverywhere they are sold. Help us do it.

　　Perrigo Nutritionals, located in Georgia, VT, is looking for a QA BatchRecord Auditor to join their Quality team.

　　The shifts needed are as follows - Tuesday - Saturday, 8am - 4:30pm

　　Scope of the RoleThe Batch Record Auditor will be responsible for auditing batch recordsand resolving non-routine exceptions and accompanying paperwork toassure that raw material and finished product batches were produced incompliance with cGMPs and to assure that the product meets currentacceptable specifications.

　　Audits internal and 3rd party batch records to ensure that batchesare manufactured and/or packaged according to approved SOPs. Assurethat specified sampling and testing is complete, acceptable, andaccounted for prior to batch disposition, and that cGMP errors areresolved, and quality incident investigations closed out.Review raw material records to ensure specifications and testingrequirements are met.Works extensively in SAP by restricting, rejected, releasing,segregating and verifying accuracy of inventory.Work closely with internal, as well as sub-contract manufacturingProduction, Packaging, QC and QA personnel to address production andtesting concerns.Follow cGMPs, SOPs and Work Instructions.Logging finished product for testing and ensuring appropriate testsare assigned.Assist with manufacturing deviation investigations. Other duties asassigned.Experience RequiredA successful candidate will have:

　　Ability to work independently and/or with minimum supervisionagainst multiple deadlines.Excellent oral and written communication skills, and stronginterpersonal skills.Strong attention to detail.Strong analytical skills.Able to work and build relationships across functional departments.Excellent multi-tasking skills and flexibility to handle changingpriorities.Required Experience

　　High school diploma or GED, advanced education strongly preferred.Minimum of 1 year experience in quality and operations.Minimum of 3 years\' experience working in FDA regulated industry.Microsoft Office experience..Preferred Experience

　　Possess an understanding of and ability to apply cGMPs. Must be able torecognize variances from cGMPs.

　　Thorough knowledge of SOPs and be able to p\\

　　PI235403266

　　\\Perrigo is an Equal Opportunity Employer and does not discriminateagainst any applicants for employment based on their race, color,religion, sex (including pregnancy, sexual orientation, or genderidentity), national origin, age, physical or mental disability, geneticinformation, veteran status, uniformed service member status, or anyother status p rotected by law.