Sr. Engineer 35409

Inteldot

$80K — $110K *
Pharmaceuticals & Biotech
Less than 5 years of experience
Job Overview by Ladders

Qualifications

  • Working knowledge of pharmaceutical/biotech processes
  • Familiarity with validation processes
  • Experience in documentation within highly regulated environments
  • Proficient in operating specialized laboratory equipment and computers
  • Understanding of GLPs and GMPs
  • Ability to apply engineering principles to production
  • Experience in developing solutions to routine technical problems

Responsibilities

  • Manage manufacturing equipment via the CMMS system including work orders and maintenance strategies
  • Collaborate with engineering staff to optimize maintenance strategies for manufacturing equipment
  • Enhance system reliability by focusing on equipment availability and reducing downtime
  • Develop metrics for equipment performance to identify improvement opportunities
  • Lead projects aimed at implementing equipment improvements
  • Act as the Subject Matter Expert for design, maintenance, and compliance operations
  • Support equipment troubleshooting and CAPAs in technical domains
  • Promote Environmental, Health and Safety compliance throughout the organization

Benefits

  • Opportunity to work on significant process and capital projects
  • Engagement in a highly regulated and dynamic environment
  • Collaboration with engineering staff and cross-functional teams
  • Leadership role in equipment improvement initiatives
  • Development of performance metrics and troubleshooting expertise
Full Job Description
Administrative Shift

Job Description:

Independently provides and/or directs the characterization of process optimization strategies and/or troubleshooting of operational issues in the operations, manufacturing, pilot plant or capital projects environment. Applies advanced and diverse engineering principles to the design and implementation of major system modifications, experiments, process and/or capital projects. Develops, organizes, analyzes and presents interpretation of results for operational issues or engineering projects of significant scope and complexity.

Requirements & Qualifications:
  • Working knowledge of pharmaceutical/biotech processes
  • Familiarity with validation processes
  • Familiarity with documentation in a highly regulated environment
  • Ability to operate specialized laboratory equipment and computers as appropriate.
  • Ability to interpret and apply GLPs and GMPs.
  • Ability to apply engineering science to production.
  • Able to develop solutions to routine technical problems of limited scope

Responsibilities:
  • Manufacturing Equipment ownership at CMMS system (Work orders approval, closing, PM strategy, spare parts' definition/accuracy/updates), reliability and change control assessments and requirements.
  • Collaborate with Engineering Staff to ensure the best maintenance strategy on manufacturing equipment operations.
  • Responsible for enhancing system reliability focusing on equipment availability, downtime reduction and maintenance optimization
  • Develop equipment performance metrics (availability, downtime, etc.) with emphasis on identifying equipment performance improvement opportunities.
  • Lead the implementation of equipment improvements project
  • SME (Subject Matter Expert) for systems regarding design, maintenance and point of contact during compliance operations
  • Support equipment troubleshooting within the functional area or in the scope of technical expertise.
  • Support deviation process and define, Implement and own CAPAs associated to equipment within area of expertise Drives Environmental, Health and Safety compliance within the organization

Education:
  • Doctorate degree or Master degree and 3 years of Engineering experience or Bachelor degree in Engineering and 5 years of Engineering experience

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