Net2Source (N2S)
Overview
Job Title: Equipment Engineer Duration: 12+ Months (Extendable) Ray Rate Range: $42.00 - $45.45/hr on W2 Base pay range: $43.00/hr - $45.00/hr Company: Net2Source Inc. is an award-winning total workforce solutions company recognized by Staffing Industry Analysts for our accelerated growth; client: One of Our Clients. Job Description
Job Title:
Equipment Engineer Duration:
12+ Months (Extendable) Ray Rate Range:
$42.00 - 45.45/hr on W2 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. Executes requalification on Controlled Temperature Units (e.g., refrigerators, freezers (-20°C / -80°C), incubators, cryotanks, cryopods, and storage rooms/areas). 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. Authors and supports the development, revision, and review of written Standard Operating Procedures (SOP) for calibration, preventive maintenance, and performance verification of instruments/equipment. Escorts and supervises vendors for calibration, preventative maintenance, performance verification and repair functions as required per current scheduling (CMMS) System. The duties/responsibilities shall include but not limited to the following: 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 updates CMMS documentation as required. Prepares reports and keeps records on calibration inspection, testing, and repairs. Executes requalification on Controlled Temperature Units (e.g., refrigerators, freezers (-20°C / -80°C), incubators, cryotanks, cryopods, and storage rooms/areas). Manages and trains the calibration technicians. Directs and assists technicians during equipment issues and repairs. Supports multiple sites within Warren. 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 SOPs 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 site customers and outside vendors while promoting a positive team environment. Participates actively in special projects as required. Ensures low cost of the Laboratory Systems Management (LSM) department by reducing overtime and implementing innovative ideas. Plans, justify and implement cost reduction small projects. Uses several test equipment and tools (e.g., pressure gauges, temperature/humidity meters, flow meters, particle counters, temperature mapping equipment). 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. Supports the development, review and approval of calibration and maintenance plans in site CMMS system. Follows cGMP (current Good Manufacturing Practices) and ALCOA principles (Attributable, Legible, Contemporaneous, Original, and Accurate); ALCOA+ adds Complete, Consistent, Enduring, and Available data. Inventory Management
Work with Planning group to ensure system is updated as calibration, maintenance and performance verification activities are performed. Approves Change Request, Asset Inductions, and Work Requests. Approving Calibration and Maintenance forms. Perform NCR investigations. Review and approve calibration and maintenance work. Regulatory Responsibilities
Maintains all required Corporate, Facilities and EHS training as required. Adheres to all safety procedures and hazard communication. May be called upon to act as SME in both internal and regulatory audits. Qualifications
Knowledge of cGMP and good documentation practices. Knowledge of pharmaceutical, manufacturing and laboratory systems and equipment. Strong problem-solving 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 multi-tasking 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. Required 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 (e.g., centrifuges, temperature/humidity meters, balances, freezers, refrigerators etc.) Maintenance coordination / planning experience preferred. Experience working in a clinical environment preferred. Working Conditions
Physical / Mental Demands
Occasional stooping, bending, stretching, pushing, pulling, reaching, and/or lifting up to 25 lbs. Ability to sit, stand, walk, and move within workspace for extended periods. Ability to perform repetitive tasks including hand to finger manipulations, grasping, pushing, and pulling. Environmental Conditions
Environment may include working in office, laboratory, or manufacturing area. Donning proper gowning and/or PPE such as safety glasses and shoes in an environment with hazardous materials and waste will be required. Working safely and effectively when working alone or working with others will be required. Travel Requirements
Local travel is required for this position to support multiple sites. Awards and Accolades
America's Most Honored Businesses (Top 10%) Awarded by USPAAC for the Fastest Growing Business in the US 12th Fastest Growing Staffing Company in USA by Staffing industry Analysts in the US (2020, 2019, 2020) Fastest 50 by NJ Biz (2020, 2019, 2020) INC 5000 Fastest growing for 8 consecutive years in a row (only 1.26% companies make it to this list) Top 100 by Dallas Business Journal (2020 and 2019) Proven Supplier of the Year by Workforce Logiq (2020 and 2019) 2019 Spirit of Alliance Award by Agile1 2018 Best of the Best Platinum Award by Agile1 2018 TechServe Alliance Excellence Awards Winner 2017 Best of the Best Gold Award by Agile1(Act1 Group) Seniority level
Mid-Senior level Employment type
Contract Job function
Engineering, Manufacturing, and Science Industries: Biotechnology Research and Pharmaceutical Manufacturing Referrals increase your chances of interviewing at Net2Source (N2S) by 2x Get notified about new Equipment Engineer jobs in
Warren, NJ .
#J-18808-Ljbffr
Job Title: Equipment Engineer Duration: 12+ Months (Extendable) Ray Rate Range: $42.00 - $45.45/hr on W2 Base pay range: $43.00/hr - $45.00/hr Company: Net2Source Inc. is an award-winning total workforce solutions company recognized by Staffing Industry Analysts for our accelerated growth; client: One of Our Clients. Job Description
Job Title:
Equipment Engineer Duration:
12+ Months (Extendable) Ray Rate Range:
$42.00 - 45.45/hr on W2 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. Executes requalification on Controlled Temperature Units (e.g., refrigerators, freezers (-20°C / -80°C), incubators, cryotanks, cryopods, and storage rooms/areas). 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. Authors and supports the development, revision, and review of written Standard Operating Procedures (SOP) for calibration, preventive maintenance, and performance verification of instruments/equipment. Escorts and supervises vendors for calibration, preventative maintenance, performance verification and repair functions as required per current scheduling (CMMS) System. The duties/responsibilities shall include but not limited to the following: 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 updates CMMS documentation as required. Prepares reports and keeps records on calibration inspection, testing, and repairs. Executes requalification on Controlled Temperature Units (e.g., refrigerators, freezers (-20°C / -80°C), incubators, cryotanks, cryopods, and storage rooms/areas). Manages and trains the calibration technicians. Directs and assists technicians during equipment issues and repairs. Supports multiple sites within Warren. 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 SOPs 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 site customers and outside vendors while promoting a positive team environment. Participates actively in special projects as required. Ensures low cost of the Laboratory Systems Management (LSM) department by reducing overtime and implementing innovative ideas. Plans, justify and implement cost reduction small projects. Uses several test equipment and tools (e.g., pressure gauges, temperature/humidity meters, flow meters, particle counters, temperature mapping equipment). 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. Supports the development, review and approval of calibration and maintenance plans in site CMMS system. Follows cGMP (current Good Manufacturing Practices) and ALCOA principles (Attributable, Legible, Contemporaneous, Original, and Accurate); ALCOA+ adds Complete, Consistent, Enduring, and Available data. Inventory Management
Work with Planning group to ensure system is updated as calibration, maintenance and performance verification activities are performed. Approves Change Request, Asset Inductions, and Work Requests. Approving Calibration and Maintenance forms. Perform NCR investigations. Review and approve calibration and maintenance work. Regulatory Responsibilities
Maintains all required Corporate, Facilities and EHS training as required. Adheres to all safety procedures and hazard communication. May be called upon to act as SME in both internal and regulatory audits. Qualifications
Knowledge of cGMP and good documentation practices. Knowledge of pharmaceutical, manufacturing and laboratory systems and equipment. Strong problem-solving 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 multi-tasking 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. Required 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 (e.g., centrifuges, temperature/humidity meters, balances, freezers, refrigerators etc.) Maintenance coordination / planning experience preferred. Experience working in a clinical environment preferred. Working Conditions
Physical / Mental Demands
Occasional stooping, bending, stretching, pushing, pulling, reaching, and/or lifting up to 25 lbs. Ability to sit, stand, walk, and move within workspace for extended periods. Ability to perform repetitive tasks including hand to finger manipulations, grasping, pushing, and pulling. Environmental Conditions
Environment may include working in office, laboratory, or manufacturing area. Donning proper gowning and/or PPE such as safety glasses and shoes in an environment with hazardous materials and waste will be required. Working safely and effectively when working alone or working with others will be required. Travel Requirements
Local travel is required for this position to support multiple sites. Awards and Accolades
America's Most Honored Businesses (Top 10%) Awarded by USPAAC for the Fastest Growing Business in the US 12th Fastest Growing Staffing Company in USA by Staffing industry Analysts in the US (2020, 2019, 2020) Fastest 50 by NJ Biz (2020, 2019, 2020) INC 5000 Fastest growing for 8 consecutive years in a row (only 1.26% companies make it to this list) Top 100 by Dallas Business Journal (2020 and 2019) Proven Supplier of the Year by Workforce Logiq (2020 and 2019) 2019 Spirit of Alliance Award by Agile1 2018 Best of the Best Platinum Award by Agile1 2018 TechServe Alliance Excellence Awards Winner 2017 Best of the Best Gold Award by Agile1(Act1 Group) Seniority level
Mid-Senior level Employment type
Contract Job function
Engineering, Manufacturing, and Science Industries: Biotechnology Research and Pharmaceutical Manufacturing Referrals increase your chances of interviewing at Net2Source (N2S) by 2x Get notified about new Equipment Engineer jobs in
Warren, NJ .
#J-18808-Ljbffr