
Quality Assurance Associate
Winchester, KYFull-time$7.25/hrSeen 3mo agoSeen in employer's feed today
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Job overview
Ampcus, Inc is hiring a Quality Assurance Associate. Ampcus Inc. is seeking a highly motivated Quality Assurance Associate to join their team in Winchester, KY. This role involves evaluating the compliance of analytical documentation with applicable GMP regulations and systems, requiring independent decision-making and minimal supervision. The ideal candidate will demonstrate excellent critical thinking, organizational skills, and professional communication.
Key focus areas include Review analytical release and stability data with minimal supervision and Review and approve controlled documents such as protocols, test methods, and specifications.
Successful candidates bring 3+ Years GMP Industry Experience and Bachelor's In Chemistry Or Biochemistry. Important skills include GMP Regulations, GMP Systems, Problem Solving, Organizational Skills, Professional Communication, and Effective Communication.
Skills & qualifications
Skills
Qualifications
Full job description
Experience Required
3 - 20 years
Minimum Education Required
Bachelor's Degree
Compensation
$7.25 / hourly
Hours Per Week
40
Number Of Positions
1
Work Schedule and Shift Requirements
First (Day)
Job Description
Ampcus Inc. is a certified global provider of a broad range of Technology and Business consulting services. We are in search of a highly motivated candidate to join our talented Team. Job Title: Quality Assurance Associate. Location: Winchester, KY. Description:
A QA Associate must be familiar with applicable GMP regulations and systems and have the ability to make independent decisions based on those requirements.
This individual will be responsible for evaluating the compliance of analytical documentation such as test methods, protocols, and stability and release data with minimal supervision.
This individual must demonstrate excellent critical thinking and organizational skills. Professional, effective, and proactive communication with peers, management, and interdepartmental colleagues is required.
Essential Duties and Responsibilities include the following. Other duties may be assigned.
Review of analytical release and stability data, with minimal supervision.
Review and approval of controlled documents such as protocols, test methods, and specifications.
Education and/or Experience:
Minimum of 3 years of applicable GMP industry experience. Analytical laboratory, QC laboratory, Manufacturing, QA experience may be considered applicable.
BS science degree, preferably in Chemistry or Biochemistry.
Ampcus is an Equal Opportunity Employer. All qualified applicants will receive consideration for employment without regard to r ace, color, r eligion, s ex, s exual orientation, gender identity, national origin, age, protected veterans or individuals with disabilities.
Ampcus is an Equal Opportunity Employer. All qualified applicants will receive consideration for employment without regard to r ace, color, r eligion, s ex, s exual orientation, gender identify, national origin, age, protected veterans or individuals with disabilities.
Job Type
Full time
Benefits Offered
Not specified
Veteran Preference
No
Place of Work
On-site
Requisition ID
26-03874
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