Manufacturing Quality Associate (MQA) - 2nd & 3rd shift
Quick Summary
Job Summary: The Manufacturing Quality Associate is responsible for ensuring quality and compliance during the day-to-day operations in the manufacturing environment by partnering with operations,
The Manufacturing Quality Associate is responsible for ensuring quality and compliance during the day-to-day operations in the manufacturing environment by partnering with operations, supply chain, engineering, quality control, or other functions to support product quality. This role provides GMP oversight through guidance against internal SOPs, WI, Protocols and Records as it pertains to manufacturing activities for development and commercial manufacturing.
Responsibilities
~2 min read- →BS degree required preferably in chemistry, biochemistry, or related science field.
- →5+ years of related experience in the pharmaceutical, biotechnology, or medical device industry responsibility preferred.
- →Demonstrated knowledge of quality systems, GMPs, industry standards, and regulatory requirements for the manufacture, testing, and release of pharmaceutical products.
- →Formal training in Quality disciplines (auditing, engineering, process improvement) as demonstrated through certification (ASQ, Lean Six Sigma, etc) highly preferred
- →Technical proficiency at reviewing/auditing production records, reports and/or GMP related documentation.
- →Ability to work within a team environment and willingness to contribute to the overall goals of the company.
- →Ability to lead project teams
- →Ability to handle multiple assignments and projects with competing priorities while independently managing time is critical.
- →Good organizational skills, high level of attention to detail, excellent oral and written communication skills with the ability to interact at all levels.
- →Must be willing to work off hour shifts and weekends as necessary.
The above statements are intended to describe the general nature and level of the work being performed by employees assigned to this position. This is not intended as an exhaustive list of all responsibilities, duties, and skills required. Aquestive reserves the right to make changes to the job description whenever necessary.
As part of Aquestive’s employment process, final candidate will be required to complete a drug test and background check prior to employment commencing.
Aquestive provides equal employment opportunities to all colleagues and applicants for employment and prohibits discrimination and harassment of any type without regard to race, color, religion, age, sex, national origin, disability status, genetics, protected veteran status, sexual orientation, gender identity or expression, or any other characteristic protected by federal, state or local laws.
Location & Eligibility
Listing Details
- Posted
- September 29, 2026
- First seen
- September 29, 2026
- Last seen
- October 1, 2026
Posting Health
- Days active
- 1
- Repost count
- 0
- Trust Level
- 56%
- Scored at
- October 1, 2026
Signal breakdown
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