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  • ID
    #28711461
  • Job type
    Per Hour
  • Salary
    TBD
  • Source
    StarrTrax
  • Date
    2021-12-31
  • Deadline
    2022-03-01

Vacancy expired!

Continuous Improvement Lead (Sterile Production)


LOCATION: SCHOTT Pharmaceutical Packaging (Lebanon, PA)


COMPENSATION: 75,000 to 90,000


SUMMARY / OBJECTIVE:The Continuous Improvement Lead (Sterile Production), together with the Process and Reliability Lead, owns the key systems and leading indicators across all production shifts as well as the overall results of the production line, includingsafety, quality, engagement and productivity. The CI Lead (Sterile Production) is responsible to ensure standard work is applied on a 24h basis and implemented systems are implemented to detect and correct deviations can be easily identified and corrected.
The CI Lead (Sterile Production) is expected to:

  • Leadership and Skill Development:

    • Motivate and inspire the operating teams to complete all operating objectives by also meeting Quality and Safety requirements.
    • Lead and coordinate resource requirements based on production demands, quality, material, and cost.
    • Communicate effectively within the organization and builds rapport across all shifts and all levels / supporting functions (Quality, Maintenance, SCM).
    • Provide on-the-floor coaching of equipment owners across all shifts and attends the planned stop daily.
    • Collaborate with the Process and Reliability leads in data-driven decision making, direction setting and plan for the day, week, month and quarter.
    • Increase the effectiveness of the Area Lead Team by coaching and challenging the Process and Reliability Lead with regards to results as well as daily goals.
    • Provide Skill Development/Technical Mastery/Coaching and Training.
    • Provide input into performance reviews for operational team members.

  • Shop Floor Management and Skill Development:

    • Define clear outcomes for the shop floor mgmt. meetings and ensure adherence
    • Facilitate and improve the effectiveness of the daily Process Control Meetings (PCS 1-2-3) and the weekly shop floor mgmt. meetings.
    • Develop the area 90-Day Plans to address losses and build capability.
    • Champion TPM activities, Teams, Safety, and Quality objectives for their respective area.

  • Standard Work, Problem Identification and Solving:

    • Accountable for following all Quality, Safety and Company policies, systems and standards
    • Actively look for best-practice examples within the site or externally and implement in Sterile Production
    • Own and continuously improve the CIL management system (Cleaning, Inspection, Lubrication) and enable operators to find and record deviations in the TAG system.
    • Understand and support the continuous improvement of the following systems:

      Centerlines (CL), Out of Control Action Plan (OCAP), TAG, Breakdown Analysis (BDA)

    • Perform systematic problem identification and solving by applying Six Sigma / Lean methods (e.g. DMAIC, A3, Fishbone, Kaizen workshops)
    • Act as an active part within the Problem Escalation Matrix to help resolve problems in production within the expected time.
    • Address deviations through the CAPA process in CPro.

  • Technical- and Process-Knowledge:

    • Advanced understanding of the area’s technical as well as process capabilities
    • Carry out the necessary actions/steps to ensure new products conform to the internal, and customer specifications, and that new products fall within the site’s manufacturing process capabilities.
    • Implement technical and process improvements through the Change Request process in CPro.
    • Monitor the quality in the production process to prevent quality failures and ensure compliance with company policies, GMP’s, and government regulations and policies.

ATTRACTIVE SKILLS/EXPERIENCES:

  • BS/BA Degree in relevant field (engineering preferred)
  • Lean / Six Sigma Certification (highly preferred)
  • Relevant experience (2+ years) in manufacturing setting (cleanroom setting preferred)
  • Exposure to ISO 9001, ISO 14001 an cGMP (highly preferred)
  • Demonstrated experience in leading change and situation leadership.
  • Demonstrated proficiency with MS Office, SAP and MES
  • Ability and willingness to work on a Production Floor setting in an ISO5 Cleanroom environment with full gowning and moderate noise
  • Ability and willingness to work normal business hours with w/ flexibility (e.g., OT, Weekends, On-Call) to support 24/7 operations

Vacancy expired!

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