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Job Details

GlaxoSmithKline (GSK)

QA Associate I (12:00pm - 8:30pm) (501170-gsknch)





Lincoln, Nebraska, United States

Site Name: USA - Nebraska - Lincoln
Posted Date: Apr 18 2022

Sign-On Bonus $2,000

Are you energized by a quality assurance role that allows you to accelerate compliance in a state of the art manufacturing environment? If so, this QA Associate I role could be an ideal opportunity to explore.

As a QA Associate I, you will be responsible for supporting activities to ensure product and process compliance with regulatory agencies’ requirements and company standards.

This role will provide YOU the opportunity to lead key activities to progress YOUR career, these responsibilities include some of the following:

  • Quality review & approval of GMP documents to ensure requirements are met.

  • Support implementation and sustainment of quality systems that may include (e.g.).

  • Systems & Documentation (e.g. batch records, procedures, work instructions, protocols, reports, etc.).

  • Support the execution of deviations, CAPA, change control, complaints and other quality systems as applicable

  • Support the audit and inspection processes.

  • Maintain knowledge and understanding of cGMPs, product types, and any additional training requirements for assigned tasks.

  • Provide quality oversight and guidance as directed for operations, quality control, warehouse and all other departments at the site, ensuring compliance to local procedures and cGMPs.

  • Identify and support implementation of continuous improvement opportunities.

  • Adhere to all safety guidelines and procedures.

  • Perform additional tasks as assigned.

EHS Responsibilities:

  • Know, understand and comply with all Environmental, Health, and Safety (EHS) guidelines

  • Report unsafe conditions

  • Report all injuries, illnesses and hazardous materials releases

  • Wear personal protective equipment

  • Attend EHS training programs

  • Follow all safe work procedures

Quality Responsibilities:

  • Adhere to all Quality Compliance standards (Data Integrity, QA, and QC, etc.)

  • Adhere to QMS policy and regulatory requirements.

Why you?

Basic Qualifications:

We are looking for professionals with these required skills to achieve our goals:

  • Bachelor’s degree OR Associate's degree and 2+ years of experience in a regulated GMP environment OR High school diploma and 5+ years of experience in a regulated GMP environment.

Preferred Qualifications:

If you have the following characteristics, it would be a plus:

  • Associate's degree or higher.

Why Consumer Healthcare?

Right now, we’re on an incredible journey as we prepare to become the first independent, 100% focused consumer healthcare company. We’re doing this at a time when the work we do has never mattered more. Better everyday health is about improving the health and wellness of the consumers that we touch every year – over a billion and a half of them – and it goes beyond products. It’s about truly helping people manage their health proactively in different ways as consumer needs evolve.

With category leading brands such as Sensodyne, Voltaren and Centrum, built on trusted science and human understanding, and combined with our passion, knowledge and expertise, we’re uniquely placed to do this and to grow a strong, successful business.

This is an exciting time to join us and help shape the future. It’s an opportunity to be part of something special.

Diversity, Equity and Inclusion

In Consumer Healthcare we embrace our diverse workforce by creating an inclusive environment that celebrates our unique perspectives, generates curiosity to create unmatched understanding of each other, and promotes fair and equitable outcomes for everyone.

We’re striving to create a climate where we celebrate our diversity in all forms by treating each other with respect, listening to different viewpoints, supporting our communities, and creating a workplace where your authentic self belongs and thrives.


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