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Senior Quality Assurance Associate

Avara Pharmaceutical Technologies -
Norman, OK

Quick Apply

Job Details

Full-time
$61,000 - $66,000 a year
12 days ago

Benefits

Paid training
Paid jury duty
Health insurance
Dental insurance
401(k)
Flexible spending account
Tuition reimbursement
Paid time off
On-the-job training
Vision insurance
401(k) matching
Life insurance

Qualifications

Computer operation
Teamwork
Microsoft Excel
Interpersonal skills
Computer literacy
Drug regulation
English
GMP
Bachelor's degree
Attention to detail
Pharmaceutical company experience
Quality assurance experience within pharmaceutical industry
Regulatory/legal compliance standards in production
Data-driven problem-solving
Pharmaceutical manufacturing facility experience

Full Job Description

Company Overview
Avara Pharmaceutical Technologies, Inc. is a trusted contract manufacturing partner dedicated to delivering high-quality products with regulatory compliance and on-time, in-full supply. We prioritize our people as the foundation of our success and foster a collaborative, quality-driven environment.

Job Summary
We are seeking a motivated and detail-oriented Senior Quality Assurance Associate to join our team. In this vital role, you will lead quality audits, oversee quality control processes, and ensure the integrity of our manufacturing operations. Your expertise will help maintain the highest standards of quality systems, support continuous improvement, and ensure compliance across all facets of production.

Purpose & Scope:

Review and approve batch records, deviation investigations, and reports. Provide inter- and intradepartmental support in the preparation and review of documentation related to and including manufacturing processes, equipment, and computer systems that affect GMP-related activities.

Administers the QA deviation and CAPA system, internal audit system, supplier audit system, and all other necessary quality systems. Provides GMP guidance to other departments and project teams.

Essential Job Responsibilities:

Assist in the investigation, reporting, and resolution of major deviations
Review and approval of validation protocols and reports
Review and approval of all GMP document revisions including SOP's, MPR's, specifications, test methods, etc.
Administration of the deviation and CAPA system
Administration of the internal audit and supplier audit program
Performance of internal and external audits
Host and support for audits of APT by third parties, Avara corporate, and all regulatory bodies
Review and approval of CAPA plans and completion
Follow up on CAPA and deviation to ensure effectiveness
Representation of QA on site-wide and regional and global project teams
Provide GMP guidance to all affected departments at APT
Development and preparation of all QA metrics and reporting the results to APT and regional and global management (Q10)
Development and administration of APT OJT and GMP training program
Use of statistical analysis tools to evaluate data
Development and use of risk assessment tools

Quantitative Dimensions:

This position has direct impact on batch processing and release, disposition of materials and components, approval and disposition of minor and major level deviations, the compliance state of APT, and site wide project support. This position has direct interaction with international regulatory agencies, APT suppliers and vendors, and other Avara affiliates and departments. This position has an indirect impact on Avara-wide compliance and other company-wide projects.

Organizational Context:

Reports to the Manager of Quality Assurance
No direct reports

Qualifications:

Required

3-5 years previous experience with GMP within the pharmaceutical industry
3-5 years direct QA experience
Good verbal and written communication skills with basic computer skills.
Attention to detail and accurate record keeping.
Able to multi-task.
Basic understanding and knowledge of GMPs and the pharmaceutical industry, quality practices and standards
Experience with statistical data analysis preferred
Must be able to read, write and understand the English language (statement common to allJob Descriptions)
Must be able to work independently with some supervision.
Must be able to gather and evaluate data to make sound decisions.
Must be able to exercise judgment in the resolution of problems.
Office environment; must be able to sit at a desk for extended periods of time.
Occasionally requires ability to climb stairs and the ability to perform while wearing required personal protective equipment, such as respiratory protection, eye protection, hearing protection and safety shoes.
Knowledge of CFR parts 210 &211
Experience with Microsoft programs (Excel, Word, etc.)

Preferred

Bachelor’s degree

Pay: $61,000.00 - $66,000.00 per year

Benefits:

401(k)
401(k) matching
Dental insurance
Flexible spending account
Health insurance
Life insurance
On-the-job training
Paid jury duty
Paid time off
Tuition reimbursement
Vision insurance

Application Question(s):

Do you now, or will you in the future, require sponsorship for employment visa status (e.g., H-1B visa status, etc.) to work legally for our Company in the United States?

Education:

Bachelor's (Required)

Experience:

QA & GMP: 3 years (Required)

Ability to Commute:

Norman, OK 73072 (Required)

Ability to Relocate:

Norman, OK 73072: Relocate before starting work (Required)

Work Location: In person

Quick Apply

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