Are you ready to be part of an exciting journey as a key player in a hybrid Pharma/Medical Device manufacturing site entering full commercial production?
This is a rare opportunity to contribute to cutting-edge operations in a dynamic, fast-paced environment where your expertise will help shape the future of healthcare solutions. We are looking for a skilled Quality Control Supervisor to lead and optimize the activities within the QC laboratory and support ambitious goals.
What You’ll Do:
As the Laboratory Supervisor, you will play a pivotal role in ensuring that all analytical activities are efficiently coordinated and executed within the laboratory, directly contributing to the success of our products and the satisfaction of our clients. Key responsibilities include:
* Leadership in QC Operations: Schedule, coordinate, and supervise all analytical activities within the QC laboratory, ensuring timely and accurate execution of tasks.
* Cross-functional Coordination: Partner with external departments such as Operations, PD, IPQA, and Micro to ensure that samples are submitted correctly and on time for in-process and finished product testing.
* Analytical Data Review and Reporting: Oversee the review and reporting of analytical data, providing timely updates to cross-functional teams and ensuring effective communication of results.
* Change Control & CAPA Management: Lead and coordinate change controls, CAPAs, and deviations within the QC lab, ensuring adherence to regulatory requirements and industry best practices.
* Training & Development: Coordinate and lead the training of analysts within the QC team, ensuring that the team is equipped with the necessary skills to maintain high standards.
* Method Transfer Oversight: Review and manage analytical Method Transfer protocols, ensuring their timely execution and successful integration into our operations.
* Supply Chain & Resource Management: Oversee the management of lab supplies and standards, ensuring that resources are available and optimized for routine analysis.
* Compliance & Audit Readiness: Ensure laboratory compliance with all regulatory requirements and maintain audit readiness through periodic audit trial reviews and proactive management of documentation.
* Vendor Management & Qualification: Complete vendor qualification reports and collaborate with external suppliers to ensure quality materials and services.
* Acting Senior Manager Designee: Serve as a designee for the Senior Manager of Quality Control for Material, GLP, and project-related matters.
Why You’ll Love Working Here:
This is an exceptional opportunity for you to grow your career while making a significant impact in the life sciences sector. You’ll be working with a passionate team and enjoying the following benefits:
* Career Advancement: As the company enters full commercial production, you will be part of a pivotal transition, gaining invaluable experience in scaling operations and navigating the complexities of large-scale manufacturing.
* Professional Development: We believe in continuous learning. You'll have opportunities to enhance your technical skills, participate in training, and gain exposure to industry-leading methodologies.
* Dynamic & Collaborative Environment: Work closely with cross-functional teams in Operations, Product Development, and Quality Assurance to drive process improvements and ensure product quality.
* Leadership Opportunities: As you manage a high-performing team, you will have the chance to mentor and lead analysts, fostering their growth while advancing your own career.
* State-of-the-Art Facilities: Our cutting-edge lab and manufacturing facilities provide the perfect environment for you to showcase your talents and drive innovation.
* Job Stability & Competitive Compensation: Enjoy a stable career with a competitive salary, comprehensive benefits, and a rewarding career path with significant growth potential.
What We’re Looking For:
* Bachelor’s degree in Life Sciences, Chemistry, or a related field.
* Proven experience in a QC laboratory or similar role, with a strong background in analytical testing and laboratory management.
* Strong knowledge of regulatory requirements, including GMP, GLP, and industry best practices.
* Exceptional organizational and leadership skills, with the ability to manage multiple projects and prioritize effectively.
* Excellent communication and interpersonal skills, with the ability to collaborate across departments.
* Experience in Change Control, CAPA, and Deviations management is highly desirable.
* Familiarity with analytical methods and the ability to execute and manage Method Transfers.
* Experience in resource planning and vendor qualification processes is a plus.
Ready to Take the Next Step in Your Career?
If you are a results-driven professional with a passion for quality control and analytical testing, we invite you to join our team during this exciting time of growth and transition.
Apply now to be part of a transformative journey in the Pharma/Medical Device industry, where your contributions will directly impact the success of our products and the lives of those who rely on them.
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