Sr Engineer - 35333

Mirus Consulting Group

$75K — $95K *
Pharmaceuticals & Biotech
Less than 5 years of experience
Job Overview by Ladders

Qualifications

  • Doctorate in Engineering, OR
  • Master's degree in Engineering with 2+ years of relevant experience, OR
  • Bachelor's degree in Engineering with 4+ years of relevant experience
  • Experience in packaging processes within regulated environments (pharmaceutical, biotech, or medical devices)
  • Strong knowledge of GMP, FDA, EMA regulations, and industry standards

Responsibilities

  • Develop and implement C&Q strategy aligned with project and regulatory requirements.
  • Lead risk assessments to determine qualification scope.
  • Execute commissioning activities, including FAT, SAT, and field commissioning.
  • Ensure systems operate according to design specifications.
  • Author and approve qualification protocols (IQ/OQ/PQ).
  • Ensure C&Q documentation complies with GMP, FDA, EMA, and internal standards.
  • Collaborate with Engineering, Validation, QA, Manufacturing, and Supply Chain teams.

Benefits

  • Technical coaching and mentorship opportunities for junior engineers
  • Comprehensive exposure to cross-functional collaboration
  • Involvement in critical risk management and change control processes
  • Hands-on experience with packaging system qualification in a regulated environment
  • Potential for career growth within the C&Q field
Full Job Description
Position Summary
The Senior Engineer is responsible for leading Commissioning & Qualification (C&Q) activities for packaging systems, ensuring compliance with regulatory requirements and alignment with project objectives. This role provides technical leadership in developing strategies, executing qualification protocols, and supporting cross-functional teams throughout the project lifecycle.

Key Responsibilities
  1. C&Q Strategy & Planning
    1. Develop and implement the overall Commissioning & Qualification strategy aligned with project and regulatory requirements.
    2. Define system boundaries and classify direct and indirect impact systems.
    3. Lead risk assessments (e.g., ISPE Baseline, ASTM E2500) to determine qualification scope.
    4. Develop C&Q plans, timelines, and resource forecasts.
  2. Commissioning Activities
    1. Lead and/or execute commissioning activities, including FAT, SAT, and field commissioning.
    2. Ensure systems are installed and operate according to design specifications.
    3. Coordinate with vendors, contractors, and project teams during system startup.
    4. Review and approve commissioning documentation and testing results.
  3. Qualification Execution (IQ/OQ/PQ)
    1. Author, review, and approve qualification protocols (Installation, Operational, and Performance Qualification).
    2. Maintain traceability from User Requirements Specifications (URS) through testing execution.
    3. Oversee protocol execution and ensure accurate documentation of results.
  4. Documentation & Compliance
    1. Ensure all C&Q documentation complies with GMP, FDA, EMA, and internal standards.
    2. Manage documentation lifecycle within electronic systems.
    3. Apply and enforce data integrity principles (ALCOA+).
    4. Prepare and support validation summary reports.
  5. Risk Management & Change Control
    1. Lead and document risk assessments related to system qualification.
    2. Evaluate and manage change controls impacting validated systems.
    3. Assess deviations and implement corrective and preventive actions (CAPA).
  6. Cross-functional Collaboration
    1. Collaborate with Engineering, Validation, Quality Assurance (QA), Manufacturing, and Supply Chain teams.
    2. Interface with system owners and technical authorities.
    3. Provide technical coaching and mentorship to junior engineers.
    4. Support project meetings, status updates, and stakeholder communications.
  7. Process Characterization
    1. Develop characterization protocols.
    2. Execute characterization studies for packaging processes.
    3. Prepare and review characterization reports.
Qualifications
  • Doctorate in Engineering, OR
  • Master's degree in Engineering with 2+ years of relevant experience, OR
  • Bachelor's degree in Engineering with 4+ years of relevant experience
Preferred Qualifications
  • Experience in packaging processes within regulated environments (pharmaceutical, biotech, or medical devices).
  • Strong knowledge of GMP, FDA, EMA regulations, and industry standards.
  • Familiarity with risk-based validation approaches (ASTM E2500, ISPE).
  • Excellent technical writing, problem-solving, and communication skills.

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