Process Engineering Manager

3 weeks ago

College Station, Texas, United States Mentor Technical Group Full time

Job Summary

Mentor Technical Group is seeking a highly skilled Process Engineering Manager to join our team. As a Process Engineering Manager, you will be responsible for providing technical support and solutions for the FDA-regulated industry.

Key Responsibilities

  • Provide engineering, troubleshooting support and technical expertise for process equipment and site utilities as needed.
  • Proactively identify engineering problems or opportunities and apply technical expertise to develop and present feasible solutions.
  • Lead and manage new equipment/systems installation including infrastructure, connectivity and capacity assessments.
  • Lead and manage process improvements, corrective and preventive actions (CAPAs) and change controls implementation for process equipment and site utilities.
  • Work with process sciences in developing new equipment/systems/process design, controls, requirements, specifications and drawings.
  • Liaison with CAPEX team for the implementation of capital projects.
  • Coordinate execution of projects, improvements and other engineering activities.
  • Oversee contractors when implementation and/or corrections are required.
  • Works with QA/QC to ensure proper testing, inspection and release after completion of engineering activities.
  • Support equipment IQ/OQ/PQ or any other validation/commissioning startup activity as required.
  • Ensure new equipment operates in compliance with required EHS, regulations and codes.
  • Develop, write, edit and/or review in collaboration with Facilities SOPs, P&IDs and maintenance procedures for new equipment and/or systems.
  • Communicate efficiently with Contractors, Suppliers, OEM providers as well as internal equipment owners and operators for a successful operation of the FDBT facility.
  • Able to work with other contractors, manufacturing, validations and quality control personnel regarding changes or improvements to the systems.
  • Ensure compliance, as set forth in internal quality protocols and SOPs including cGMP and FDA regulatory guidelines, within the areas of responsibility, and document out of specification conditions with deviations, CAPAs and Change Controls as appropriate.
  • Continuously stay current with assigned SOPs and keep up to date training file ensuring compliance with all applicable Standard Operating Procedures.
  • Ensure a safe work environment is maintained through adherence and compliance with safety guidelines, policies, site procedures and job performance qualifications.
  • Able to identify potential problem areas of equipment that is malfunctioning, using technical manuals or mechanical, electrical or controls knowledge.

Requirements

  • Must be flexible and able to manage multiple priorities and tasks.
  • Must be results driven and goal oriented with the ability to manage risks.
  • Knowledge and understanding using P&IDs, equipment manuals, specifications, SOPs, and be able to use proper judgment when implementing projects or taking corrective actions during equipment malfunctioning.
  • Possess or have the ability to apply these skills to resolve technical problems and to gain knowledge with respect to the operation and maintenance of various utility/process systems.
  • Must be able to develop, and draft operational procedures and maintenance procedures for technical (utilities/process) equipment using the OEM manual and system knowledge.
  • Must be able to use project management software such as Microsoft Project. Proficient with MS Office products (Word, Excel, Outlook, PowerPoint).
  • Knowledge of regulatory requirements for manufacturing of pharmaceutical products.
  • Ability to organize and present technical overviews to engineering staff, cross functional departments, and upper management.
  • Ability to learn quickly and work effectively with little supervision when needed.
  • Desire to work in a fast paced, state of the art, alternately research and customized manufacturing facility.
  • Knowledge of bio-medical, bio-technical equipment, both upstream and downstream highly desirable.
  • Bachelor's Degree preferably in Electrical, Chemical, Mechanical or Biomedical Engineering
  • Six (6) years of qualified experience in an engineering role in an FDA regulated research or manufacturing facility

Working Conditions

While performing the duties of this job, the employee is regularly required to use hands to finger, handle, feel, or operate equipments, tools, or controls.

He / she may frequently work inside weather conditions, near moving mechanical parts, exposed to wet and or humid conditions, and an odorous atmosphere, may be exposed to fumes and the risk of electrical shock, and occasionally work on ladders in high places, in small spaces, such as lift/metering stations, manholes, tanks and wet wells.

Mentor Technical Group is an equal opportunity employer, and all qualified applicants will receive consideration for employment without regard to race, color, religion, sex, sexual orientation, gender identity, genetic information, national origin, protected veteran status, disability status, or any other characteristic protected by law.

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