Equipment Engineer

Job Title : Equipment Engineer

Duration : 12 months Contract (Possible extension based on work performance)

Location : Warren, NJ 07059

Onsite / Hybrid : Onsite

Job Description :

1. PURPOSE AND SCOPE OF POSITION :

The LSM Equipment Engineer supports the successful operation of laboratory and clinical manufacturing operations at their home sites through interaction with internal team members and internal customers, and external service providers. The incumbent conducts tasks assigned by the management independently or with minimum supervision. The LSM Equipment Engineer is responsible for initiating and owning deviations, CAPAs, and change controls, and authoring calibration and maintenance SOPs as well as performing calibrations, maintenance, and qualifications / validations.

2. 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 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.

3. 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 -20 C / -80 C 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.

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 Request.

Approving Calibration and Maintenance forms.

Perform Client s 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.

4. 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.

5. 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.

This job description is intended to describe the general nature and level of work being performed by the person assigned to this position. The primary duties and responsibilities are intended to describe those functions that are essential to the performance of this job.

This job description does not state or imply that the above are the only duties and responsibilities assigned to this position. There are other duties and responsibilities that are considered incidental or secondary to the overall purpose of this job. Employees holding this position will be required to perform any other job-related duties as requested by management.

Additional Job Requirements :

Position Handles Hazardous Materials