Manager, QC

at  Thermo Fisher Scientific

Millersburg, PA 17061, USA -

Start DateExpiry DateSalaryPosted OnExperienceSkillsTelecommuteSponsor Visa
Immediate24 Jan, 2025Not Specified24 Oct, 20245 year(s) or aboveManufacturing Processes,Customer Requirements,Excel,Working Experience,TeamsNoNo
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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