A new world-leading consumer health company, shaped by all who join us. We're improving everyday health for billions of people by growing and innovating our global portfolio of category-leading brands.
Job Description:
We are recruiting for a Senior Quality position on site, acting as an independent advisor to the Site Director and the Senior Leadership Team (SLT) regarding Quality and Compliance. This position has management responsibility for Quality Assurance and Quality Control for the manufacturing facility producing Medicinals, Medical Devices, and intermediate bulk products with worldwide distribution.
Responsibilities:
* Provide direction and support for product quality and compliance matters
* Direct all quality related functions for the manufacturing facility, including commercial product release
* Ensure implementation of Consumer Healthcare Quality standards and current GMP requirements within the site Manufacturing plant
* Deploy Quality and Compliance systems (HQS) and ensure they are in place and in use
* Develop continuous improvement practices
* Keep the site ready for external Health Authority inspections and monitor the site inspection readiness status
* Manage inspections and audits
* Guarantee corrective and preventative actions are completed as per committed timelines and are effective
* Evaluate and follow up on the appropriateness and completeness of corrective action plans until closure
* Escalate site major quality related topics using the real time escalation system
* Proactively identify and manage the site quality and compliance risks, using the Consumer Health Risk Management System (RMS) and adequate governance
* Monitor Key Quality Performance Indicators for the site
* Identify trends and use the Site Quality council to define quality improvement plans
* Investigate quality issues using applicable root cause analysis and problem-solving methods to avoid repeat deviations
* Implement Right First-Time principles for continuous improvement across compliance systems and process operations
* Lead and provide quality expertise assessment for sourcing and business development initiatives to ensure selections adhere to current quality / compliance guidelines
* Drive the site Quality culture, and ensure all functions have the capabilities to work in a pharmaceutical environment
Requirements:
* Bachelor's/Master's degree in chemistry, pharmacy, Biology or Related science
* Ability to manager stakeholder, make independent quality decisions and stand for quality
* 5 years relevant experience in a regulated pharmaceutical industry in the area of manufacturing and quality
* Professional experience in QA, GMPs, in the pharmaceutical field, Quality Systems and Operations
* Excellent communication, planning and organization skills
* Good knowledge of analytical laboratory activities
* Knowledgeable in auditing and inspection against regulatory / quality standards
* Excellent interpersonal and leadership skills, managing people and stakeholders, driving cross functional improvement projects and executing corporate programs
About Us:
Haleon is a new world-leading consumer health company, shaping our future together with diverse perspectives and creating an inclusive environment where everyone can thrive. We believe in treating each other with respect, listening to different viewpoints, supporting our communities, and creating a workplace where your authentic self belongs and thrives. If flexibility is important to you, we encourage you to explore what opportunities are available. We are an Equal Opportunity Employer and will treat your information confidentially.