Production Engineer II

Padagis LLC

$85K — $110K *
Pharmaceuticals & Biotech
5 - 7 years of experience
Job Overview by Ladders

Qualifications

  • Bachelor's degree in engineering or related field.
  • 5+ years of experience in production or manufacturing.
  • Subject Matter Expert (SME) on manufacturing equipment.
  • Proven leadership in leading complex projects.
  • Strong problem-solving and decision-making skills.
  • Excellent communication and interpersonal skills.
  • Proficiency in productivity and statistical analysis tools.

Responsibilities

  • Identify and analyze process inefficiencies in production.
  • Develop SOPs, MBRs, and OMs to standardize best practices.
  • Lead large-scale continuous improvement initiatives aligned with KPIs.
  • Utilize tools like SPC and DOE to solve manufacturing challenges.
  • Mentor and coach junior engineers for skill development.
  • Evaluate and integrate emerging technologies to enhance efficiency.
  • Monitor operational performance and report metrics to leadership.

Benefits

  • Opportunities for professional growth and development.
  • Collaborative culture fostering team success.
  • Access to training in continuous improvement methodologies.
  • Engagement with advanced technologies and methodologies.
  • Active involvement in strategic organizational goals.
Full Job Description
We are seeking an experienced Production Engineer with a strong focus on Continuous Improvement to join our team in New Hope, MN. In this role, you will be focused on driving large-scale, strategic process improvement initiatives across the manufacturing network. This role encompasses leading cross-functional teams, advising on advanced engineering problems, and influencing broader organizational goals. Level 2 engineers are responsible for designing and executing high-impact projects, mentoring lower-level engineering staff, and contributing to long-term operational strategies.

Job duties:

Strategic Process Improvement Leadership

  • Identify and analyze process inefficiencies in the production of bottled liquids, tablets, suppositories, and tubed products.
  • Develop standard operating procedures (SOPs), Master Batch Records (MBR's), and Operations Manuals (Oms) to drive best practices across manufacturing lines.
  • Actively participate in structured training programs focused on pharmaceutical production, lean tools, and continuous improvement methodologies.
  • Lead large and complex continuous improvement initiatives, ensuring alignment with business goals and Key Performance Indicators (KPIs).
  • Drive long-term operational improvements by identifying systemic inefficiencies and applying cutting-edge engineering and lean techniques.
  • Collaborate with senior leadership to develop and implement overarching strategies for operational excellence.


Advancing Continuous Improvement Practices

  • Utilize advanced tools such as Statistical Process Control (SPC), Design of Experiments (DOE), and Failure Mode and Effects Analysis (FMEA) to solve complex manufacturing challenges.

  • Identify and execute cost-saving initiatives to improve efficiency and reduce waste, documenting measurable outcomes.

  • Serve as a subject matter expert in lean manufacturing and Six Sigma tools, introducing new methodologies and fostering a culture of continuous improvement.


Cross-Functional Leadership and Mentorship

  • Mentor and coach junior engineers, ensuring skill development and long-term professional growth.

  • Act as a key resource for problem-solving and decision-making, working alongside managers and department heads.


Innovation and Technology Integration

  • Evaluate and integrate emerging technologies, automation solutions, and best practices to enhance production efficiency.

  • Collaborate with R&D and engineering departments to implement process innovations and scalable solutions for existing and new product lines.


KPI Tracking and Reporting

  • Monitor, analyze, and report operational performance metrics to senior leadership.

  • Develop dashboards and tools to track progress against organizational goals, including cost savings, quality improvements, and production efficiency milestones.


Project Management

  • Work with multidisciplinary teams to execute high-complexity medium to large scale improvement projects.

  • Track the progress and ensure timely delivery of assigned workstreams.

  • Measure results and provide cost-benefit analysis of improvement initiatives.


Compliance and Documentation

  • Maintain compliance with Good Manufacturing Practices (GMP), FDA standards, and other applicable regulations.

  • Ensure accurate documentation of process adjustments, deviations, and corrective actions as required.

  • Lead efforts to improve documentation and standard operating procedure (SOP) adherence.

  • Support audits and regulatory inspections by presenting and explaining findings and implemented improvements.

  • Ensure all collected and reported data complies with Good Manufacturing Practices (GMP) and FDA regulatory standards.

  • Complete assigned documentation tasks related to corrective actions, process changes, and improvement logs.


Production Support

  • Collaborate with production teams to troubleshoot and resolve process-related issues in manufacturing.


  • Assist in ensuring that all production lines meet quality, regulatory, and safety standards.


  • Play an active role in reducing downtime, waste, and variation in processes while maintaining product quality.


  • Engage with on-floor production teams to understand day-to-day challenges and provide input to improve efficiencies on a basic level.


  • Provide Subject Matter Expert (SME) guidance to set-up technicians and assist with training and troubleshooting activities in manufacturing.


Minimum qualifications:

  • Bachelor's degree in an engineering discipline (mechanical, chemical, industrial, electrical) or a related field.
  • Five or more (5+) years of experience in a production or manufacturing environment.
  • Subject Matter Expert (SME) on manufacturing equipment.
  • Strong track record of leading complex, high-impact projects.
  • Demonstrated strong problem-solving, decision-making, and leadership skills.
  • Excellent communication, collaboration, and interpersonal skills.
  • Proficiency in productivity tools (Excel, SAP, statistical analysis tools, etc.)


Preferred qualifications:

  • Production or manufacturing experience in pharmaceutical industry.
  • Certification in lean manufacturing, Six Sigma (Green Belt or equivalent).


Core competencies:

Since its beginning, Padagis has been undergoing the process of identifying what we believe will lead to the success of our organization in a competitive landscape. To that end, we have developed a set of five "core" competencies. We strive to bring employees on board the journey with us who exemplify these key competencies:

  • Service delivery - Understand who your internal and external customers are, identify their needs, and deliver value above their expectations...
  • Active collaboration - Seek opportunities to work together across teams, function, business units, and geographies to seek success...
  • Demonstrate agility - Proactively identify changes in our environment and act quickly, leading or embracing change...
  • Think differently - Create, develop, and implement new ideas, products, services, or processes that involve introducing something new or significantly improving something that already exists...
  • Excellent execution - Achieve outstanding results in all aspects of our organization, including our culture, leadership, strategy, and processes...


What's Next:

At Padagis a real recruiter AND the hiring manager will review your application, not just a bot. This means we pay special attention to each application submitted for the position. While it could take a couple of days for us to get back with you, please know that we appreciate you applying for the open position and ask that you monitor your email for updates.

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