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Full-time QA Validation Specialist - Drug Manufacturing - Spartanburg, SC

at Jobisite in South Carolina

As key member of Drug Manufacturing Quality team, participate in qualifying facilities, utilities, manufacturing and analytical equipment in accordance to cGMP requirements.

Validate methods and equipment related to facilities, utilities, manufacturing, packaging and analytical equipment and cleaning methods.

Validate steam sterilization processes and equipment cleaning cycles.

Author cleaning protocols and standard operation procedures related to facilities, utilities, instrumentation, processing and drug manufacturing equipment, packaging materials and packaging machinery.

Fast growing organization offers an industry competitive compensation package, tuition reimbursement, full medical benefits, 401(k) retirement plan, company vehicle and cell phone, annual bonuses, short and long term disability insurance, professional development opportunities, and more!

For complete details contact Christopher Moreno at:
(609) 584-9000 ext 264

Or submit resume online at:
dmc9.com/cam/app.asp

Or email to:
1000042731_10007349 AT najbcareers303.com

Please reference #39195159 when responding.

Education Requirements: Bachelor Degree
Minimum Experience Requirements: 2-5 years
Job City Location: Spartanburg
Job State Location: SC
Job Country Location: USA
Salary Range: $80,000to $120,000

Diedre Moire Corporation, Inc.
Diedremoire_dot_com

WE ARE AN EQUAL OPPORTUNITY EMPLOYER and our employment decisions are made without regard to race, color, religion, age, sex, national origin, handicap, disability or marital status. We reasonably accommodate individuals with handicaps, disabilities and bona fide religious beliefs. Jobs Career Position Hiring. CONSIDERED EXPERIENCE INCLUDES: Cleaning Validation Engineer QA Validation Quality Assurance Pharmaceutical Manufacturing cGMP #DiedreMoire #QAjobs #CleaningValidation #JobSearch #JobHunt #JobOpening #Hiring #Job #Jobs #Careers #Employment #jobposting

DISCLAIMER: We will make every effort to consider applications for all available positions and shall use one or more of the contact methods and addresses indicated in resume or online application. Indicated location may be proximate or may be desirable point of embarkation for paid or unpaid relocation to another venue. Job descriptions may fit single or multiple presently available or anticipated positions and are NOT an offer of employment or contract implied or otherwise. Described compensation is not definite nor precise and may be estimated and approximate and is negotiable depending on market conditions and candidate availability and other factors and is solely at the discretion of employers. Linguistics used herein may use First Person Singular and First Person Plural grammatical person construction for and with the meaning of Third Person Singular and Third Person Plural references. We reserves the right to amend and change responsibilities to meet business and organizational needs as necessary. Response to a specific posting or advertisement may result in consideration for other opportunities and not necessarily the incentive or basis of the response. Nothing herein is or may be considered a promise, guarantee, offer, pledge, agreement, contract, or oath.

If you submit an application or resume which contains your email address, we will use that email address to communicate with you about this and other positions. We use an email quality control service to maintain security and a remove and dead address filter. To cancel receiving email communications, simply send an email from your address with the word "remove" in the subject line to pleaseremove_AT_candseek4.com Or, visit the website at jobbankremove_dot_com. If you have further concern regarding email received from us, call (609) 584-5499.

Reference : QA Validation Specialist - Drug Manufacturing - Spartanburg, SC jobs


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Published at 07-01-2020
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