Process Engineer

Keystone Industries

$80K — $96K *
Manufacturing & Automotive
Less than 5 years of experience
Job Overview by Ladders

Qualifications

  • 3-5 years of experience as a process engineer in FDA-regulated manufacturing
  • Knowledge of cGMP requirements and ISO standards
  • Experience with process improvements and validation in regulated environments
  • Proficiency in developing and executing validation plans
  • Strong troubleshooting and problem-solving skills
  • Effective communication and cross-functional collaboration abilities
  • Bachelor's degree in Chemical Engineering or related field

Responsibilities

  • Develop understanding of manufacturing processes and troubleshoot using technical tools
  • Support process validation, including development of IQ, OQ & PQ protocols
  • Collaborate to create quality documentation such as CAPAs and NCRs
  • Manage projects providing technical support throughout product lifecycle
  • Identify and implement process and equipment improvements
  • Review and approve technical documentation related to processes and equipment
  • Lead root cause analysis for quality issues and performance improvements

Benefits

  • Health, Dental, and Vision Insurance
  • 401(k) Retirement Plan
  • Paid Time Off and Holidays
  • Professional Development Opportunities
  • Health and Wellness Programs
  • Flexible Work Environment
Full Job Description
Position Details:
  • Title: Process Engineer
  • Schedule: 8:00 am - 4:30 pm M-F
  • Location: Gibbstown, NJ (08027)
  • Ideal Candidate: The ideal candidate will have a minimum of 3-5 years related experience in a manufacturing.
  • Salary/Pay Range (based on experience and qualifications): $80,000+

Essential Job Functions:
  • Develops a fundamental understanding of the processes and equipment. Utilizes technical and engineering tools to troubleshoot and understand the process.
  • Support validation efforts for manufacturing processes, equipment, and systems, including commissioning and qualification activities and the development/execution of IQ, OQ & PQ protocols, compliant with existing SOPs.
  • In collaboration with other personnel, develop and write CAPAs, NCRs, process deviations, and other quality documentation to ensure quality and efficient production of regulated products.
  • Manage projects and participate in applicable project core teams and extended teams, providing technical engineering support from concept through implementation and start-up.
    • Interface regularly with quality control, quality assurance, production, engineering, analytical and R&D personnel
    • Provide cross-functional support by sound and timely decision making utilizing statistical and problem-solving tools
  • Contribute to the process and equipment design of new and existing manufacturing processes, including scale-up, technology transfer, process optimization, and commercialization activities.
  • Identifies, recommends, and implements process improvements
    • Identify and specify the purchase of new equipment for process improvements
    • Utilizes quality systems for validation of new equipment
  • Review and approve process- and equipment-related technical documentation, including specifications, drawings, protocols, reports, and change controls.
  • Lead root cause analysis and corrective actions to establish plans to reduce cost of poor quality.
  • Act as the point of contact for troubleshooting/problem solving of quality upsets.
  • Assists in prioritizing maintenance and operational activities to maintain production schedules.
  • Identifies scope of capital projects to improve safety, quality, reliability, and production.
  • Identify and support opportunities for manufacturing cost reductions.
  • Improves process throughput. Utilizes modeling tools to identify bottlenecks and proposes operational or equipment modifications to improve throughput.
  • Scale-up and first production of new products and processes. Key member of project teams to introduce new products into production and provide first samples to customers.
  • Routinely assesses process using measurements and data interpretation. Utilizes statistical tools to analyze process data to ensure process is in control and capable.
  • Support future Engineering and Quality initiatives.
  • Perform research as needed.
  • Perform additional duties/tasks as needed or requested by management.

Qualifications:
  • 3-5 years' experience in a process engineering role involved in the manufacture of FDA-regulated products.
  • Knowledge of cGMP requirements and ISO standards.
  • Experience supporting process improvements, equipment implementation, validation activities, and manufacturing start-up initiatives in a regulated environment.
  • Experience developing and executing validation plans and procedures.
  • Knowledge of IQ/OQ/PQ protocols.
  • Knowledge of process-related standards.
  • Familiarity with engineering drawings, process flow diagrams (PFDs), and related technical documentation.
  • Strong mechanical aptitude.
  • Strong problem-solving and troubleshooting skills.
  • Ability to navigate ambiguous situations; flexible and adaptable.
  • Collaborative attitude and strong interpersonal skills with the ability to communicate effectively and work cross-functionally at all levels, both internally and externally.
  • Strong organizational and decision-making skills.
  • Demonstrated project management skills with the ability to successfully manage multiple priorities simultaneously.
  • Proven ability to perform under deadlines and adjust plans to meet changing business needs.
  • Computer proficiency including Microsoft Office Suite, ERP systems, and related software.
  • Self-starter with strong initiative, dependability, and the ability to work with minimal supervision.

Desired Skills:
  • Experience in a cGMP manufacturing environment.
  • Lean Manufacturing and/or Six Sigma methodologies.
  • Experience with batch manufacturing, process scale-up, and product commercialization.
  • Familiarity with AutoCAD, SolidWorks, or similar engineering software.
  • Microsoft D365.

Education/Certifications:
  • Bachelor of Science in Chemical Engineering or related discipline.

Safety:
  • Comply with all safety regulations; maintains a safe work environment at all times.
  • Adhere to always wearing the proper PPE/Safety equipment.
  • Understand and comply with all written safety, health, and environmental procedures.
  • Attend all required scheduled Health, Safety and Environmental training sessions.
  • Participate in required Health, Safety and Environmental initiatives and programs.
  • Perform required administrative functions related to Health, Safety and Environmental functions such as completing forms, checklists, and log sheets.

Physical Demands and Work Environment:

The physical demands and work environment characteristics described here are representative of those that must be met by an employee to successfully perform the essential functions of this job.
  • Physical Demands: Employee is required to walk; stand; sit; use hands and fingers to manipulate objects, tools, or controls; reach with hands and arms; balance; stoop; bend; kneel and climb; and occasionally lift/move up to 50 lbs. In addition, may seldomly be required to maneuver and move 30 to 55-gallon drums and up to 450 pounds utilizing proper ergonomic handling equipment and/or the proper techniques.
  • Work Environment: This position is located in a manufacturing facility. Employees frequently work near moving mechanical equipment. Noise intensity level: moderate to loud. Employees may work with hazardous contaminants. This role requires one to work both in an office and manufacturing environment; certain job functions may need to be performed in a cleanroom environment. Employees must adhere to all Personal Protective Equipment (PPE) and gowning requirements.


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