QC Finished Goods Supervisor page is loaded
QC Finished Goods Supervisor
Apply locations: Nyon Main Site | Time type: Full time | Posted on: Posted 13 Days Ago | End Date: May 5, 2025 (7 days left to apply) | Job requisition id: 530797
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, Panadol, Advil, Voltaren, Theraflu, Otrivin, and Centrum – through a unique combination of deep human understanding and trusted science. We’re achieving this in a company that we’re in control of, in an environment we’re co-creating, with a culture that’s uniquely ours. Care to join us? It isn’t a question.
This is an exciting time to join us and help shape the future. It’s an opportunity to be part of something special.
Job purpose:
The purpose of the Supervisor role is to develop and lead a department to consistently deliver outstanding safety, quality, service, and value. The supervisor manages Team Leader, Scientist, and Senior Analysts of the department. This role is crucial in ensuring that the business strategy is executed through an engaged, motivated, and capable team. The role will ensure that our site maintains the highest standards in Environment, Health, Safety, and Wellness (EHSW) and Quality while achieving objectives of the Nyon site.
Key Responsibilities:
EHS Responsibilities – All Associates
* Know, understand, and comply with all Environment, Health, and Safety (EHS) guidelines. Report unsafe conditions, all injuries, illnesses, and hazardous materials releases. Wear personal protective equipment, attend EHS training programs, and follow all safe work procedures.
Quality Responsibilities – All Associates
* Adhere to all Quality Compliance standards (Data Integrity, Deviation, Lab Investigation, etc.) including QMS policy and regulatory requirements.
Job Responsibilities
* Compliance: Ensure compliance with EHS, cGMP, and Quality standards. Conduct safety and quality investigations as needed. Lead by example in adhering to company policies and procedures. SME during audits.
* People Leadership: Full leadership of a team of scientists, Team Leaders, and Senior Analysts within a fast-moving consumer goods (FMCG) production environment, ensuring adherence to safety, quality, compliance, and output standards.
* Process Management: Establish and confirm standards (4M’s: Material, Manpower, Method, Measurement) for managing safety, quality, and output. Serve as primary contact for PCT. Approve Analytical Assessments (ICH Q3D, Q3C, sVMP…), analytical protocols, and reports. Ensure timely delivery of analytical activities related to VMP and Pharmacopeia remediations. Provide data to anticipate analytical activities (SRM program).
* Performance Management: Use problem-solving and performance management tools. Drive real-time issue identification, resolution, and continuous improvement initiatives. Lead investigations for complex lab investigations/deviations. Schedule activities related to Finished Product and QC validation (QC Smart). Provide KPIs. Support new project implementations (e.g., new software, robots). Coordinate FG activities (QC Smart) with the Team Leader.
* Talent Development: Identify and develop key talent, ensuring regular development plans. Set performance expectations and provide feedback.
* Resource Management: Oversee task assignment, staffing, and recruitment efforts.
* Project Implementation: Coach and support improvement projects, managing scope, schedule, and costs.
Knowledge/ Education/ Experience Required
* High School Diploma or equivalent with 10 years of relevant experience in a laboratory environment / Master’s Degree in Science, Engineering, or related field.
* 10 years in a leadership role within a regulated laboratory environment (e.g., pharmaceutical, FMCG).
* Preferred: Experience in an FDA-regulated environment, GMP requirements, project management, SAP.
* Computer skills: Excel, Word, PowerPoint.
* Understanding of Root Cause Analysis.
* Strong interpersonal, communication, coaching, and problem-solving skills.
* Ability to lead teams through change and drive continuous improvement.
* Ability to work in a fast-paced environment with minimal supervision.
* Proactive attitude.
Care to join us? Find out what life at Haleon is really like at www.haleon.com/careers.
At Haleon, we embrace diversity by creating an inclusive environment that celebrates unique perspectives, fosters curiosity, and promotes fair outcomes. We strive to create a workplace where your authentic self belongs and thrives. We believe in an agile working culture. If flexibility is important, explore with our hiring team the opportunities available.
As you apply, we will ask for some voluntary personal information to help us consider a diverse pool of candidates and meet our inclusion and diversity goals. This information will be kept confidential and not accessible to hiring managers.
Haleon is an Equal Opportunity Employer. All qualified applicants will receive consideration without regard to race, color, religion, sex, sexual orientation, gender identity, age, disability, or other protected classes.
Accommodation Requests
If you require accommodations during the application process, please inform your recruiter with specific details. We will provide necessary support confidentially.
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Who are we?
Hello. We’re Haleon, a leading consumer healthcare company. We’re committed to improving health globally through our trusted brands, including Sensodyne, Panadol, and others. Join us to be part of a co-created environment and culture that’s uniquely ours.
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