Hello. We’re Haleon. A new world-leading consumer health company. Shaped by all who join us. Together, we’re improving everyday health for billions of people. By growing and innovating our global portfolio of category-leading brands – including Sensodyne, Advil, Voltaren, Theraflu, and Centrum – through a unique combination of deep human understanding and trusted science. What’s more, we’re achieving it in a company that we’re in control of. In an environment that we’re co-creating. And a culture that’s uniquely ours. Care to join us. It isn’t a question.

QA Associate I

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.

Key Responsibilities:

• 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:

• BENEFIT ELIGIBLE DATE OF HIRE: medical, dental, vision, annual bonus, 401(k) w/company contribution, vacation, parental leave, identity theft and MORE !

• Associate's degree or higher in a science related field.

Diversity, Equity and Inclusion

At Haleon 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. We believe in an agile working culture for all our roles. If flexibility is important to you, we encourage you to explore with our hiring team what the opportunities are.