Sr. Engineer 35611

Inteldot

$88K — $105K *
Pharmaceuticals & Biotech
Less than 5 years of experience
Job Overview by Ladders

Qualifications

  • Working knowledge of pharmaceutical/biotech processes
  • Familiarity with validation processes
  • Familiarity with documentation in a highly regulated environment
  • Experience operating specialized laboratory equipment and computers
  • Ability to interpret and apply GLPs and GMPs
  • Ability to apply engineering principles to production
  • Skilled in developing solutions for routine technical problems.

Responsibilities

  • Oversee manufacturing equipment management via CMMS, including work orders and preventive maintenance strategy.
  • Collaborate with engineering teams to devise optimal maintenance strategies for equipment.
  • Enhance system reliability focusing on equipment availability and maintenance optimization.
  • Develop performance metrics for equipment, identifying improvement opportunities.
  • Lead projects aimed at equipment improvements and system modifications.
  • Act as Subject Matter Expert (SME) for systems in design and maintenance compliance.
  • Support troubleshooting efforts and manage deviations, implementing corrective actions as needed.

Benefits

  • Opportunities for professional development and continuing education
  • Collaborative work environment
  • Access to advanced engineering projects
  • Engagement in compliance and regulatory affairs
  • Support for achieving work-life balance.
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 projects
  • 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 OR Masters + 2 years of Engineering experience OR Bachelor's in engineering + 4 years of Engineering experience.

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