Email Alert for
ⓘ There was an unexpected error processing your request.
Please refresh the page and try again.
If the problem persists, please contact us with your issue.
You can always manage your preferences and update your interests to ensure you receive the most relevant opportunities.
Get ready to discover your next great opportunity.
Englewood Lab, Inc
Totowa
+ Conducts Annual Drug (Product) Reviews and Device History Reviews. + Maintains Regulatory Compliance documents and documents of external origin. + Maintain Document Control (including Records Retention) + Participates in internal and external audit process. + Participates in Mock (product) recall audits. + Maintain SOPs and Quality Forms as part
Job Source: Englewood Lab, IncPSG Global Solutions Careers
East Hanover, NJ, United States
Apply now and our proprietary system will quickly have you in front of a live recruiter. The Opportunity Description We're looking for a Quality Assurance Associate , working in Pharmaceuticals and Medical Products industry in 1 Health Plaza, #Bldg 200, East Hanover, New Jersey, 07936, United States . Interaction with both Quality organizatio
Job Source: PSG Global Solutions CareersPSG Global Solutions
East Hanover, NJ, United States
Description We're looking for a Quality Assurance Associate , working in Pharmaceuticals and Medical Products industry in 1 Health Plaza, #Bldg 200, East Hanover, New Jersey, 07936, United States . Interaction with both Quality organization as well as other supporting functions such franchises and Drug Safety. Responsibilities include proj
Job Source: PSG Global SolutionsPSG Global Solutions
, NY, United States
Description We're looking for a Quality Assurance Associate , working in Pharmaceuticals and Medical Products industry in 1 Health Plaza, #Bldg 200, East Hanover, New Jersey, 07936, United States . Interaction with both Quality organization as well as other supporting functions such franchises and Drug Safety. Responsibilities include proj
Job Source: PSG Global SolutionsActalent
Fairfield, NJ, United States
Urgently hiring a Quality Assurance Specialist! Job Description: This person will be reviewing data from personal care product manufacturing and determine why products don't meet specs. This person will be responsible for CRM Clean-up and Data Migration clean-up They will review all compliance documentation for personal care products They will
Job Source: ActalentRK Pharma Inc.
Pearl River, NY, United States
Benefits: 401(k) Competitive salary Dental insurance Health insurance Opportunity for advancement Paid time off Training & development Vision insurance RK Pharma Inc, a US based company with subsidiaries in India, is seeking multiple Quality Assurance Associates to complement our existing Quality Assurance team as we scale towards commerci
Job Source: RK Pharma Inc.Sterling Life Sciences
Fort Lee, NJ, United States
Job Description Our client, a leading pharmaceutical company, is currently recruiting an Associate Director of Quality Assurance who will infuse the Quality Assurance Team with their talent, energy and leadership skills. This is an exceptional opportunity to join a corporate culture that is known for its innovative and growth-oriented vision. Resp
Job Source: Sterling Life SciencesNYC Health Hospitals
New York, NY, United States
Empower Every New Yorker - Without Exception - to Live the Healthiest Life Possible NYC Health + Hospitals is the largest public health care system in the United States. We provide essential outpatient, inpatient and home-based services to more than one million New Yorkers every year across the city's five boroughs. Our large health system consist
Job Source: NYC Health HospitalsTotowa, NJ, United States
Conducts Annual Drug (Product) Reviews and Device History Reviews.
Maintains Regulatory Compliance documents and documents of external origin.
Maintain Document Control (including Records Retention)
Participates in internal and external audit process.
Participates in Mock (product) recall audits.
Maintain SOPs and Quality Forms as part of Document Control.
Maintains records of customer-approvals documents as evidence of authenticity.
Participate in QA Audits and draft reports of such audits.
Effects changes to specification sheets as approved through change control requests.
Support Change Control program and maintain evidence of product and process changes.
Maintains SOP binders and updates such documents through approved CCs.
Supports EWL Employee training and documentation.
Maintains suppliers and vendors qualification program.
Supports and maintains approvals of formulary, specifications and manufacturing records.
Participates in Mock (product) recall audits.
Maintains Records Retention for QA Dept.
Initiates, Tracks, and authors Annual Drug Reviews (ADRs) for OTC and Annual Drug Reviews and Device History Reviews (DHRs).
Assists in collating, reviewing, filing, maintaining of OTC bulk batch records, COAs, formula documents, etc.
Tracks and Performs physical sample retain review for ADRs and DHRs.
Tracks, Maintains, Closes requests for Change Control Notices (CC), Defective Material forms (DMF), and Deviations, Return Authorizations, Investigations, etc.
Requirements
Minimum of 2 years of diploma program or 4-year college degree
2 to 3 years industry or related experience.
Previous experience in Pharma, Cosmetics, food, medical device, or allied profession
Good Technical Writing ability.
Excellent knowledge of Word, Excel, Access, and other Windows-based programs
Good record-keeping skills.
Benefits
Medical, Dental, and Vision Insurance
Life Insurance paid 100% by the company
401K after 6 months
Email Alert for Quality Assurance Associate- (Quality) jobs in Totowa, NJ, United States
ⓘ There was an unexpected error processing your request.
Please refresh the page and try again.
If the problem persists, please contact us with your issue.
You can always manage your preferences and update your interests to ensure you receive the most relevant opportunities.
Get ready to discover your next great opportunity.