Quality Manager - Analytical Science & Technology

Hello. We’re Haleon. A world-leading consumer healthcare company with a clear purpose to deliver better everyday health with humanity. Our leading brands – including Sensodyne, Panadol, Advil, Theraflu, Otrivin, and Centrum - are built on science, innovation and human understanding and are trusted by millions of consumers globally. What’s more, we’re achieving it in a company that we’re in control of. We are achieving it in an environment where we co-create, and in a culture that’s uniquely ours.

About the Role:

We are seeking a talented and experienced Associate Quality Manager to join the Analytical Science & Technology (AS&T) QA team. This role offers the opportunity to work on a variety of projects and work cross-functionally to provide quality support for GxP activities. The areas of project support include analytical method development, validation, transfer, and testing as well as supporting AS&T laboratory operations. The role will also involve supporting the Global Documentation Group (GDG) to review and approve manufacturing documentation updates.

Key responsibilities:

• Provide quality review and approval for AS&T GxP activities, ensuring compliance to local procedures and cGMPs.

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

• Support the execution and/or approval of deviations, CAPA, change control, and other quality systems as applicable.

• Support (review, update, approve) commercial quality documentation updates (e.g., Master Formulation, Master Manufacturing Instruction, Finished Product, Intermediate/Bulk and Raw Material Specifications) within Veeva Quality docs for Haleon commercial and contract manufacture supply chain sites.

Basic Qualifications:

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

• Previous experience in an FDA regulated industry.
• Knowledge of cGMPs and FDA regulatory requirements.
• Strong working knowledge of pharmaceutical and Consumer Healthcare manufacturing processes, QC laboratory operations, and analytical method development/validation/transfer.
• Experience with QA support for GxP operations
• Electronic documentation storage system experience (e.g., Veeva or similar)
• Competency using Word, Excel and PowerPoint (Office 365)
• Ability to handle numerous tasks simultaneously and prioritize activities

Preferred Qualifications:

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

• Knowledge of document management in the drug manufacturing industry
• Experience with change controls
• Ability to perform/assess data analysis and root cause analysis to support deviation investigations, corrective and preventive actions and process improvements.
• Strong interpersonal, communication and organizational skills

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.

Care to join us. Find out what life at Haleon is really like www.haleon.com/careers/
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.
As you apply, we will ask you to share some personal information, which is entirely voluntary. We want to have an opportunity to consider a diverse pool of qualified candidates and this information will assist us in meeting that objective and in understanding how well we are doing against our inclusion and diversity ambitions. We would really appreciate it if you could take a few moments to complete it. Rest assured, Hiring Managers do not have access to this information and we will treat your information confidentially.
Haleon is an Equal Opportunity Employer. All qualified applicants will receive equal consideration for employment without regard to race, color, national origin, religion, sex, pregnancy, marital status, sexual orientation, gender identity/expression, age, disability, genetic information, military service, covered/protected veteran status or any other federal, state or local protected class.

Accommodation Requests

If you require a reasonable accommodation or other assistance to apply for a job at Haleon at any stage of the application process, please let your recruiter know by providing them with a description of specific accommodations you are requesting. We’ll provide all reasonable accommodations to support you throughout the recruitment process and treat all information you provide us in confidence.