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Process Equipment Engineer

Location : Morris Plains NJ US 07950
Job Type : Direct
Reference Code : 20565-JF1
Compensation : 120000.00 - 125000.00 USD/YEAR
Start Date : 05/11/2021
Hours : Full Time
Required Years of Experience : 8
Required Education : BS Engineering or Science
Travel : No
Relocation : No
Job Industry : Pharmaceutical

Job Description :


  • Permanent position for a Process Equipment Engineer responsible for understanding the manufacturing processes and equipment to meet the needs of existing and new products.

  • Interface with end users to ensure scope, deliverables and expectations are clearly defined.

  • Involve all stake holders for proper collaborative results.

  • Review FS, URS and other support documentation for correctness.

  • Plan, schedule, coordinate and perform activities for engineering functions and partners.

  • Coordinate production equipment projects within budget and in accordance with assigned timelines.

  • Responsible for the continuous improvements of production equipment utilizing Good Engineering Practices (GEP) and change management procedures.

  • Provide redline drawings for updating and issuance within change management process following applicable drawing management procedures.

  • Maintain schedule integrity for projects related to production equipment and their support.

  • Clean utilities following Good Engineering Practices (GEP) and design.

  • Plan, prioritize and coordinate execution of work with affected departments and vendors.

  • Ensures all safety requirements are reviewed and in place before work is executed.

  • Provide frontline engineering support to all phases of production, from the time the issue is recognized until solved and communicate properly to end users.

  • Perform Root Cause Analysis for incidents and investigations, then perform execution of steps to prevent them (CAPA).

  • Provide safety work permit and verify staff and contractor training on Safety Health & Environmental procedures.

  • Ensure adherence to safety SOPs when executing maintenance activities.

  • Review/approve documentation to ensure accurate, concise documentation is submitted and meets all cGMP requirements and internal SOP's.

  • Implement CAPAs and Deviation / Investigation Planning and complete records on time.

  • Implement reliability based engineering strategies carried out up to standards (internal and external standards).

  • Ensure high level of performance for production equipment and ancillary support subsystems.

  • Organize engineering work to reduce unexpected emergencies by managing optimization and expansion project plans.


Required Qualifications :


  • BS Engineering or Science related discipline.

  • Current experience in leading problem solving and resolution within production line environments.

  • Must be familiar and able to utilize applicable industry standard and guidelines as well as answering any challenges to the standards (GxP, PDA, ISPE, EU Annex 1, electrical code, etc.).

  • Minimum 8 years of pharmaceutical industry or related engineering experience.

  • Experience with troubleshooting and root cause analysis coupled with CAPA implementation.

  • Proven experience in coordination of complicated engineering tasks.

  • Knowledge and hands on experience production systems.



Contact: John Forsatz


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