Quality Assurance Associate

Jabil Inc.•Hunt Valley, MD

45d•$21 - $39

About The Position

At Jabil we strive to make ANYTHING POSSIBLE and EVERYTHING BETTER. We are proud to be a trusted partner for the world's top brands, offering comprehensive engineering, manufacturing, and supply chain solutions. With over 50 years of experience across industries and a vast network of over 100 sites worldwide, Jabil combines global reach with local expertise to deliver both scalable and customized solutions. Our commitment extends beyond business success as we strive to build sustainable processes that minimize environmental impact and foster vibrant and diverse communities around the globe.

Requirements

Familiarity with Microsoft programs, such as Word, Excel, PowerPoint, Access, Project, etc.
Knowledge / Experience with electronic Quality Management Systems such as MasterControl or TrackWise
Knowledge of current federal, local, and international regulations regarding the production, testing and release of drug substances and products.
Excellent oral and written communication skills
Ability to manage multiple priorities and re-prioritize tasks as required
Excellent problem-solving and organizational skills
Bachelor's degree or higher degree preferred, or equivalent experience in the pharmaceutical industry)
Prefer one (1) year of Quality Assurance experience in a GMP-regulated industry, such as pharmaceutical, biologics, medical devices, dietary supplements, food, cosmetics or in combination with relevant education.
Ability to travel between and within facilities to visit staff, operations, and projects, as needed.
Ability to sit, stand, climb stairs, and climb ladders to mezzanines (when necessary).
Ability to lift, up to, 40 (lbs.) pounds, on occasion.
Ability to use PPE (safety shoes, goggles, respirators, gloves, etc. when necessary).

Responsibilities

To complete quality related tasks as directed by the supervisor associated with the review of operations performed within the functional area. These may include to one or several of the following quality operational tasks, product release, process quality, document control, quality systems & operations, and compliance.
To support or contribute to the preparation, review, and approval of GMP-related documentation in accordance with approved SOPs and applicable regulations (i.e., GMPs, GDPs).
To perform or assist in general organizational tasks including oversight and escalation of open tasks and timelines, document management, tracking of tasks, generation of technical reports, and reporting of quality metrics.
To ensure that appropriate quality standards are applied in accordance with regulatory, pharmacopeias, and company requirements to ensure compliance.
To assist in quality-related activities that may include the preparation and review of GMP documentation, the management of paper and electronic records in adherence to document management and retention procedures.
To escalate compliance issues appropriately and timely, when discovered.
To complete assigned training in a timely fashion to ensure that both personal and department training status remains current.
QA review of data to ensure conformance to specifications or requirements to maintain quality assurance objectives to meet regulatory requirements.
Work collaboratively with various stakeholders in the review, issuance, or providing service to ensure compliance with company and regulatory requirements.
Other duties as assigned.