Inteldot
Inteldot22h ago
New

Specialist Manufacturing 35529

PRPR·Juncosmid
OtherManufacturing
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Quick Summary

Requirements Summary

Deviations management Deviation assessments Track wise Biotech and manufacturing experience Responsibilities: Initiate, revise, and approve manufacturing procedures.

Technical Tools
OtherManufacturing

With minimal supervision, support the execution of manufacturing/quality systems such as non-conformances, process validation, procedures, training, and new product introductions. Apply process, operational, scientific expertise, basic compliance knowledge, and analytical and troubleshooting skills to support manufacturing operations. May serve as primary production process owner for process support systems and assist with process ownership responsibilities on more complex process systems.

Requirements

~1 min read
  • Deviations management
  • Deviation assessments
  • Track wise
  • Biotech and manufacturing experience

    Responsibilities

    ~1 min read
    • Initiate, revise, and approve manufacturing procedures. Ensure all procedures reflect current operations. Serve as a document owner.
    • Assess process performance by observation of floor operations and review of performance data. Evaluate, plan, and implement solutions for process improvement opportunities.
    • Provide troubleshooting support.
    • Assist in generation of training materials and may assist in providing training on scientific or technical aspects of the process.
    • Support establishment of process monitoring parameters and control limits. Collect process-monitoring data and support the assessment of deviations.
    • Provide support of timely execution of the process monitoring quarterly reports.Non-Conformance and CAPA
    • Ensure that all Non-conformances are triaged within the established goal.
    • Responsible for authoring investigation reports, execution of corrective actions and managing NC/CAPA closure within established goal.
    • Monitor and communicate incidents trends.
    • Review equipment/system Root Cause Analysis investigations and support trend evaluations.
    • Assist with generation of process validation protocols and reports and with the execution of the process validation.
    • Support collection and analysis of process validation data.
    • Participate in regulatory inspections, New Product Introductions, and Process or Equipment Modifications:
    • Participate in the NPI process to assess requirements for documentation, materials, training, and equipment modifications.
    • Assess, prioritize, justify, and provide implementation and project management support for process or equipment modification projects.
    • Assist manufacturing change owner on CCRB packages impacting the process.
    • Doctorate OR Master’s + 2 years of Manufacturing Operations experience OR Bachelors + 4 years of Manufacturing Operations experience OR Associates + 8 years of Manufacturing Operations experience OR High school/GED + 10 years of Manufacturing Operations experience

      Location & Eligibility

      Where is the job
      Juncos, PR
      On-site at the office

      Listing Details

      Posted
      July 23, 2026
      First seen
      July 23, 2026
      Last seen
      July 23, 2026

      Posting Health

      Days active
      0
      Repost count
      0
      Trust Level
      58%
      Scored at
      July 23, 2026

      Signal breakdown

      freshnesssource trustcontent trustemployer trust
      Inteldot
      Inteldot
      breezy
      Employees
      30
      Founded
      2004
      View company profile
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      InteldotSpecialist Manufacturing 35529