| Hiring- C2C contract- Equipment Engineer - Warren NJ at Warren, Texas, USA |
| Email: [email protected] |
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Processing description: http://bit.ly/4ey8w48 https://jobs.nvoids.com/job_details.jsp?id=2340940&uid= Hi Hope you are doing well! My name is Javid, and I am a Senior Technical Recruiter with MindPro Solutions Inc. Please review the job description below and share your updated resume and employer details if you find the position suitable. Role: Equipment Engineer Type: Contract Location: Warren NJ Duration: Long term contract Job description: Role: Equipment Engineer Location:100% Onsite at Warren NJ Job Type: 12 Months Contract Rate: USD 48 - 53 Hourly Must-Haves : Executes equipment calibration, preventative maintenance, performance verification, troubleshooting and repair activities in laboratory and manufacturing areas, as required per current scheduling (CMMS) System. Escorts and supervises vendors for calibration, preventative maintenance, performance verification and repair functions as required per current scheduling (CMMS) System. Reviews and approves vendor executed calibration, maintenance, repair, and performance verification records for accuracy, and completeness. Owns and supports deviations and investigations that result from calibration or performance verification activities, along with developing and supporting the implementation of corrective and preventive actions. Documents and populates calibration/maintenance information in WPT (Work Plan Template) or MDT (Measurement Data Template) using CMMS system. Executes requalification on Controlled Temperature Units (ex. Refrigerators, Freezers (which includes -20C / -80C Freezers), Incubators, Cryotanks, Cryopods, and Storage Rooms/Areas). REQUIRED COMPETENCIES: Knowledge of cGMP, GXP, GAMP, including 21CFR part 11, computer systems validation requirements and good documentation practices. Knowledge of pharmaceutical, manufacturing and laboratory systems and equipment. Knowledge of calibration management and environmental monitoring systems. Strong critical thinking skills and the ability to work independently. Excellent interpersonal and communication skills with experience dealing with a diverse workforce where individual initiative, accountability to the team, and professional maturity are required. Strong multitasking and organizational ability. Ability to effectively manage multiple tasks and activities simultaneously. Proficiency in Microsoft Office Suite Word, Excel, PowerPoint, and Outlook; innate ability to learn new software, such as corporate intranet and enterprise applications. Working knowledge of scheduling software and systems, and inventory management systems, e.g., Blue Mountain RAM and/or Maximo Computerized Maintenance Management System (CMMS) preferred. Ability to interact effectively with QC, Manufacturing, QA, and Engineering & Facilities groups. DUTIES AND RESPONSIBILITIES Operational Activities Executes equipment calibration, preventative maintenance, performance verification, troubleshooting and repair activities in laboratory and manufacturing areas, as required per current scheduling (CMMS) System. Escorts and supervises vendors for calibration, preventative maintenance, performance verification and repair functions as required per current scheduling (CMMS) System. Reviews and approves vendor executed calibration, maintenance, repair, and performance verification records for accuracy, and completeness. Documents and populates calibration/maintenance information in WPT (Work Plan Template) or MDT (Measurement Data Template) using CMMS system. Modifies or update CMMS documentation as required. Prepares reports and keeps records on calibration inspection, testing, and repairs. Executes requalification on Controlled Temperature Units (ex. Refrigerators, Freezers (which includes -20C / -80C Freezers), Incubators, Cryotanks, Cryopods, and Storage Rooms/Areas). Supports multiple sites within Warren and Summit. Supports clinical manufacturing on-call equipment troubleshooting activities during weekends as required. Ensures all calibration, PM, and performance verification records are filed appropriately after approval. Contacts supplier for quotation on external calibration/PM of the equipment and calibration standards Initiates, participates, and assists in resolution of quality investigations. Authors and supports the development, revision, and review of written Standard Operating Procedures (SOP) for calibration, preventive maintenance, and performance verification of instruments/equipment. Supports the development, review and approval of calibration and maintenance plans in site CMMS system. Supports the execution of process improvement studies, as required. Adheres to written policies and procedures governing the LSM department activities and the equipment they manage to ensure compliance with approved standards. Performs inventory of the equipment and/or standards in the labs as required. Maintains a positive relationship with the site customers and outside vendors while promoting a positive team environment. Participates actively in special projects as required. Ensure low cost of the Laboratory Systems Management (LSM) department (Reducing overtime, implementing innovative ideas) Plans, justify and implement cost reduction small projects. Usage of several test equipment and tools (e.g., pressure gauges, temperature, humidity meters, flow meters, particle counters and temperature mapping equipment etc.) Owns and supports deviations and investigations that result from calibration or performance verification activities, along with developing and supporting the implementation of corrective and preventive actions. Support the development, review and approval of calibration and maintenance plans in site CMMS system. Follows cGMP (current Good Manufacturing Practices) and ALCOA principles ('ALCOA' defines that data should be Attributable, Legible, Contemporaneous, Original, and Accurate) In addition, 'ALCOA+' guidance recommends that data is also Complete, Consistent, Enduring, and Available. EDUCATION AND EXPERIENCE BS in Engineering or Science related discipline preferred. Minimum 3 years of experience in FDA-regulated industry. Minimum 3 years of experience working directly with laboratory equipment (ex. centrifuges, temperature/humidity meters, balances, freezers, refrigerators etc.) Maintenance coordination / planning experience preferred. Experience working in a clinical environment preferred. Thanks & Regards Javid Ahmad Sr Technical Recruiter MindPro Solutions Inc E: [email protected] L: linkedin.com/in/javid-ahmad-598111158 W: www.mindprosolutions.com -- Keywords: cprogramm quality analyst access management information technology New Jersey Hiring- C2C contract- Equipment Engineer - Warren NJ [email protected] http://bit.ly/4ey8w48 https://jobs.nvoids.com/job_details.jsp?id=2340940&uid= |
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| 09:57 PM 14-Apr-25 |