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Manufacturing Team Lead, Service - Night Shift
bioMérieux Durham, NC
$114k-145k (estimate)
Full Time | Scientific Services 5 Months Ago
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bioMérieux is Hiring a Manufacturing Team Lead, Service - Night Shift Near Durham, NC

Benefits at bioMerieux:Low-cost medical, dental, and vision benefits starting day one
11 paid holidays
160 hours of paid time off
Annual bonus
9.5% 401k company contribution with no vesting period
Tuition reimbursement up to $10,000 per calendar year
Onsite cafeteria with daily food stipend

Position Summary:Normal working hours: 7:00pm - 7:30am working a 2-2-3

The Team Lead position is responsible for front-line leadership of a team engaged in the operation of high speed manufacturing/packaging equipment and/or process-driven Reagent formulation.

Primary Responsibilities:

  • Leadership
    • Serve a back up to the Supervisor (or higher) when needed
    • Develop manufacturing team
      • Inspire and motivate manufacturing team to achieve top performance as a team
      • Inspire and promote self-growth and internal development within the team
    • Assist in management of daily activities i.e; scheduling production activities & Daily shift tie-in meetings
      • Generate reports, charts and KPI's and interpret the data to identify problems, and proceed with proper decision making
      • Conduct staff meetings daily or as needed, keeping records/documentation of what is discussed
  • Production
    • Operate and maintain highly automated bottle handling, filling, vision inspection, conveying, robotic palletizing, autoclaving, and / or labeling equipment in a cGMP compliant manner, using HMI/SCADA interfaces
    • Setup high speed manufacturing equipment, within defined tolerances, to ensure product runs are started on time and within established guidelines
    • Provide feedback on design and operation of equipment to optimize manufacturing
    • Check equipment during production runs for proper performance and assures the equipment is maintaining standard speeds and process times
    • Troubleshoot simple to moderate equipment related issues
  • Quality
    • Right First Time (RFT): minimal deviations and error free performance
      • Ensure that all batch paperwork is completed in an accurate, thorough, and timely manner
      • Execute production activities per approved Manufacturing Directions while maintaining compliance with all job related SOPs
    • Assist with manufacturing deviation analysis, CAPA actions and other process equipment related quality concerns
    • Perform self-audit of rooms and processes
    • Train and certify teammates on production processes and procedures
  • Documentation / Training
    • Utilize SOP and documentation to record data manually or through identified software applications
    • Assist in the development, revision of manufacturing procedures and training programs for manufacturing employees.
    • Ensure overall team training is maintained current for processes and procedures relevant to all area activities
    • Coordinate cross-training among roles to create staffing flexibility and increased depth.
  • Safety
    • Comply with all safety policies and procedures at all times
    • Appropriately use PPE (Personal Protection Equipment) as required to perform routine and non-routine duties.
    • Monitor workers on site during production activities to ensure adherences to ethics and safety procedures
  • Continuous Improvement
    • Lead and promote continuous improvement through team and individual initiatives
      • Identify areas of deficiency and implement practices to improve employee safety and to reduce the cost incurred through excessive scrap, poor workflow/process design and others
      • Serve as a project team member to reduce scrap, increase product quality, decrease operational costs, and improve departmental efficiency/productivity
      • Serve as change agent by driving the required cultural transformation and the adoption of successful process improvement practices. Diagnoses barriers to project success and facilitates resolution
      • 5S: Maintain all work areas in a well-organized, clean and tidy manner at all times in compliance with cGMP requirements
  • Other Duties
    • Contribute to team goal development, status tracking and communication by providing feedback to the direct manager for the PMP (Performance Management Program) process
    • Work with other departments and assist with executing validation protocols associated with manufacturing/packaging equipment and procedures including revalidation as scheduled or required to maintain systems in a validated state
    • Partner with maintenance staff to perform routine and preventative maintenance activities to include inspecting, lubricating, adjusting of manufacturing equipment in a timely basis to ensure reliability and minimize the incidence of unplanned downtime to production equipment
    • Communicate with Materials Management, Production Operations, and Quality Control on a daily basis to ensure the timely and efficient production of all of our customer requirements

Education, Skills, Experience:

  • High school diploma or GED with 3 years in a regulated production/operations environment
    • Associates Degree in an applicable or Technical field or Vocational / Technical School preferred
  • Demonstrated proficiency in the operation of high speed, highly automated, production equipment preferred.
  • Knowledge of and experience in following OSHA regulations (LOTO, electrical safety, etc.) preferred.
  • Knowledge of FDA and/or GMP regulations preferred.
  • Mechanical background preferred. 

Job Summary

JOB TYPE

Full Time

INDUSTRY

Scientific Services

SALARY

$114k-145k (estimate)

POST DATE

11/23/2023

EXPIRATION DATE

05/12/2024

WEBSITE

www.biomerieux.com

HEADQUARTERS

Rio de Janeiro - RJ

SIZE

7,500 - 15,000

CEO

Kaitlyn Larrabee

INDUSTRY

Scientific Services

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About bioMérieux

bioMrieux conceives, develops, produces and markets diagnostics solutions (systems, reagents, software and services) intended for clinical and industrial applications, which determine the origin of a disease or a contamination to improve the health of patients and insure consumer safety. The company headquarters is located in Marcy-l'toile, Auvergne-Rhne-Alpes.

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