Manager, QC
at Thermo Fisher Scientific
Millersburg, PA 17061, USA -
Start Date | Expiry Date | Salary | Posted On | Experience | Skills | Telecommute | Sponsor Visa |
---|---|---|---|---|---|---|---|
Immediate | 24 Jan, 2025 | Not Specified | 24 Oct, 2024 | 5 year(s) or above | Manufacturing Processes,Customer Requirements,Excel,Working Experience,Teams | No | No |
Required Visa Status:
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US Citizen | Student Visa |
H1B | CPT |
OPT | H4 Spouse of H1B |
GC Green Card |
Employment Type:
Full Time | Part Time |
Permanent | Independent - 1099 |
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Contract to Hire – Corp 2 Corp |
Description:
JOB DESCRIPTION
About Thermo Fisher Scientific Inc.
When you join us at Thermo Fisher Scientific, you’ll be part of a team that values curiosity, drive, and a passion for exploration and discovery. With revenues of $22 billion and the largest investment in R&D in the industry, we provide our people with the resources and opportunities to make meaningful contributions to the world. Our mission is to enable our customers to create a healthier, cleaner, and safer world. As a united team of over 100,000 colleagues, we share a common set of values - Integrity, Intensity, Innovation, and Involvement - collaborating to accelerate research, solve intricate scientific challenges, drive technological innovation, and support patients in need.
QUALIFICATIONS/REQUIREMENTS:
- Bachelor’s degree (or higher) in an engineering or related science, or equivalent experience
- Minimum of 5 years of professional experience in a Science, Engineering, Quality, or Regulatory related role
- Proven experience as a people manager (direct and indirect management)
- Continuous improvement/lean processes and principles
- Ability to manage & implement changes with minimal supervision, onsite and remotely at global locations.
- Must be able to influence & negotiate with people & resolve issues.
- Ability to make rational, objective and appropriate decisions relating to company & department requirements.
- Ability to identify customer requirements and issues.
- Develop realistic solutions to meet customer needs and solve problems.
- Communicate recommendations and decisions across the organization.
- Proven knowledge of Quality Management System tools, continuous improvement methodologies, and in-depth product understanding.
- Demonstrated ability to effectively communicate non-conformances, risks, production, process controls, Corrective and Preventive Action (CAPA), and improvements
- Ability to lead in a fast-paced technical environment, absorb technical information, review technical information, and make technical decisions.
- ISO 13485 experience
- Understanding of plastics- materials, properties, manufacturing processes, and product assembly.
- Strong communication, presentation, and writing skills.
- Proficient with Windows-based systems like Microsoft tools; Word, Excel, Power Point.
Responsibilities:
- Lead multiple teams of Quality Control inspectors and technicians who complete in-process, environmental, and finished product inspections (teams across multiple shifts)
- Monitor product quality improvement to ensure execution of actions including any resulting customer communications/interactions.
- Establish & maintain quality metrics to measure progress against goals related to product inspections, environmental monitoring, and other quality programs
- Conduct and manage risk assessments associated with quality control procedures
- Provide effective oversight of the execution of the Quality Plan, Risk Management activities, and all design-related activities during the product/system lifecycles
- Interface directly with customers and internal groups
- Apply continuous improvement skills and tools to prioritize and drive projects and improvements/standardization across the network, with a focus on enhancing Quality service levels and aligning with strategic objectives.
- Mentor and support team members through their career development
- Communicate effectively both within immediate quality teams and across network and division leadership
- Help sites prepare for, and actively support, external audits (customer & regulatory) ensuring corrective/preventative actions are put in place to address identified non-conformances.
- Provide leadership to the quality function vital to ensure that strategic and annual quality planning is integrated into strategic and operating plans with broad-based interpersonal involvement.
- Ensures participation in New Product Development Process
REQUIREMENT SUMMARY
Min:5.0Max:10.0 year(s)
Pharmaceuticals
Production / Maintenance / Quality
Clinical Pharmacy
Graduate
An engineering or related science or equivalent experience
Proficient
1
Millersburg, PA 17061, USA