Manager, Quality Control Lab - #253775
Merz Aesthetics
Date: 2 weeks ago
City: Racine, WI
Contract type: Full time

About The Company
Merz is a family-owned medical device and pharmaceutical company headquartered in Germany. Our Global Technical Operations based in WI manufactures, packages and ships several innovative products so that people all over the world can live better, feel better, and look better.
Supervision/Coordination
Key Responsibilities:
Come join a company that is committed to being a trusted partner focused on our customers while not forgetting about our employees!
Merz is a family-owned medical device and pharmaceutical company headquartered in Germany. Our Global Technical Operations based in WI manufactures, packages and ships several innovative products so that people all over the world can live better, feel better, and look better.
Supervision/Coordination
Key Responsibilities:
- Manage staff including interviewing, hiring, training, and developing employees; planning, assigning, and directing work; appraising performance; rewarding and disciplining employees; addressing complaints and resolving problems.
- Independently set clear direction for all direct reports consistent with departmental needs.
- Evaluate and implement new analytical technologies per Quality System Standards, Quality System Regulations, and other company procedures around which the Quality System is developed.
- Ensure completion of all testing, including raw materials, in-process, final release, stability, environmental, biological, and special project/protocol testing in a timely manner that achieves fulfillment to commitments.
- Ensure lab investigations are timely and in compliance with current regulatory standards and expectations
- Serve as a resource for manufacturing to determine best course of action and material dispositions for investigations and unexpected occurrences.
- Lead investigations associated with product deviations, product non-conformances, CAPAs, scrap and rework, and analyzing the data for the reasons of Quality Improvement.
- Identify and implement new quality improvement initiatives / projects in accordance with cGMP / cGLP expectations to improve compliance, quality levels (reducing defects), and improve operational efficiencies.
- Work with manufacturing and other functional groups on manufacturing regulatory compliance issues.
- Lead training program by developing, coordinating, and delivering assigned training tasks.
- Serve as a liaison with the Quality, Operations, Commercial, and Project Team members.
- Update and communicate all needed issues as appropriate to facilitate understanding and rapid decision-making.
- Participate in product development and technical transfer teams as a subject matter expert on testing and quality matters.
- Participate in external audits as a subject matter expert on test method, test method validation, and test method development.
- Perform internal and vendor quality system audits.
- Perform routine walk-throughs and compliance checks to verify adherence to quality guidelines. Interact with inspectors in regulatory audits to represent area of responsibility.
- Adhere to established expenditure controls to support management of laboratory budget.
- BS in Physical Science or related field. Required
- Advanced degree (MS, PhD, etc.) in a physical science field. Preferred
- GLP/GMP experience. Required
- At least 5 years’ experience Pharmaceutical or Medical Device Laboratory. Required
- Supervision/leadership experience. Preferred
- Familiarity with cGMP regulations and FDA/USP/EP/BP/ICH guidelines. Required
- Quality experience may include quality testing (analytical chemistry/microbiology), QA/Regulatory, or Validation. Required
- Experience with FDA, European agency regulations, cGMP regulations, Laboratory Information. Required
- Knowledge of quality systems, quality techniques, current regulatory requirements and technical issues resolution. Required
- 20/20 Near Acuity Vision
- Comprehensive Medical, Dental, and Vision plans
- 20 days of Paid Time Off
- 15 paid holidays
- Paid Sick Leave
- 401(k)
- And more!
Come join a company that is committed to being a trusted partner focused on our customers while not forgetting about our employees!
How to apply
To apply for this job you need to authorize on our website. If you don't have an account yet, please register.
Post a resumeSimilar jobs
Racine Plant Controller
CNH,
Racine, WI
4 hours ago
CNH Industrial is a world-class equipment and services company dedicated to advancing the noble work of agriculture and construction workers. Driven by our shared purpose of Breaking New Ground, we are passionate about bringing Innovation, Sustainability, and Productivity to all that we do. As a truly global company, CNH Industrial’s 37,000+ employees form part of a diverse and inclusive workplace,...

Mergers & Acquisition Lead
CNH,
Racine, WI
1 week ago
CNH Industrial is a world-class equipment and services company. Driven by its purpose of Breaking New Ground, which centers on Innovation, Sustainability and Productivity, the Company provides the strategic direction, R&D capabilities, and investments that enable the success of its five core Brands: Case IH, New Holland Agriculture and STEYR, supplying 360° agriculture applications from machines to implements and the...

Digital Performance Analyst- Marketing
Johnson Outdoors,
Racine, WI
3 weeks ago
Digital Performance Analyst At Johnson Outdoors, home to some of the world’s most innovative and best-known outdoor recreation brands, we create amazing outdoor experiences - for adventurers, by adventurers. Come help shape the growth of Johnson Outdoors by supporting the digital performance strategies for our iconic outdoor brands in Fishing, Watercraft, Camping and Diving! The Digital Performance Analyst will drive optimizations...
