IPS – Integrated Project Services, Inc.

  • Job Locations US-DE-Greater Wilmington
    ID
    2019-4263
    Department
    Staffing
    # of Openings Remaining
    1
    Position Type
    W2 Temporary or Fixed Term
    Location : Location
    US-DE-Greater Wilmington
  • Position Responsibilities

    We are looking to add a Lab Equipment Validation Engineer/Specialist who will work onsite at our client in the Wilmington, DE area This project speficially deals with lab equipments and systems. The selected candidate will be apart of a team for a large project across multiple sites.

    Qualifications & Requirements

    ROLE RESPONSIBILITIES

    • Serving as validation representative for laboratory instruments and partnering with the laboratories, Quality System Administrators, Business Technology, Instrumentation and Quality Engineering on implementing new instruments at the site.
    • Initiates and leads risk assessment, gap analysis and deviation management for commissioning of, changes to or decommissioning of laboratory instruments and associated instrument control software where applicable within the Quality Control laboratories.
    • Authors cGMP risk assessments, user requirements & functional specifications, validation plans, protocols (i.e. IQ, OQ, PQ), traceability matrices, reports, addendums, decommissioning plans and other validation deliverables as required by the site validation SOPs.
    • Ensures lab instrument’s adherence to national and international regulatory guidelines on Electronic Records and Electronic Signatures and Data Integrity, cGMP, FDA 21 CFR Part 11/210/211, EU Annex 11, MHRA guidelines.  Authors protocol to challenge the main aspects of these requirements during validation to demonstrate adherence.  For systems found unable to fully comply, formulate workarounds/strategies with core stake holders to mitigate the gaps.
    • Assists the system owner with evaluating and recommending the appropriate user roles and privileges for data integrity (where applicable), writing instrument operation instructions and setting up preventive maintenance plans.
    • Completes periodic reviews of laboratory instruments and associated instrument control software with focus on change control, deviation investigations and CAPA to ensure compliance and validated state of the instrument.  Previous experience with Trackwise PR/CAPA systems preferred.
    • Reviews validation deliverables created by others for adherence to site validation SOPs and acts as validation approver as needed.
    • May supervise and/or mentor junior level engineers.
    • All other duties as assigned.

    REQUIREMENTS

    1. 5-7 years of experience in the validation of laboratory instruments including those with computerized systems attached in a biotechnology or pharmaceutical cGMP manufacturing environment
    2. Validation of laboratory instruments including those with computer system attached for instrument control (i.e. AA, FT-IR, ICP-MS, TOC, UV_Vis)
    3. Experience to configure, test and validate the system to demonstrate compliance with 21 CFR Part 11/Annex 11 as well as proposing procedural controls if the system is unable to fully meet the requirements
    4. The essence of the Part 11 regulations  is to ensure that electronic records and signatures are trustworthy, reliable, and generally equivalent to paper records and handwritten signatures.  As such the electronic records should not be susceptible to unauthorized access, alteration/modification, deletion, or other methods of falsification.  These records need to be accurate and be accessible/available for the duration of data retention period in case it is needed for regulatory or other audits.  In addition, the audit trail must capture change Data Integrity exp a must
    5. Must be able to multi-task - new projects will thrown at the worker constantly, must be able to handle all of them.

     

    Company Overview

    About Us

     

    IPS-Integrated Project Services is a global leader in developing innovative and cost effective solutions for the engineering, construction, commissioning and qualification of complex pharmaceutical and biotech research and manufacturing facilities. With technical expertise spanning R&D to pilot-scale to large-scale production, our team specializes in the technology, trends and regulatory environment to successfully deliver capital projects and improve operations. For over thirty years, we have applied unique LEAN methodologies throughout the project life cycle, continually finding ways to do things better and more efficiently, delivering higher quality and controlling costs. Headquartered in Blue Bell, PA, IPS is a multi-national company with over 1,100 professionals worldwide and offices in California, Indiana, Kansas, Massachusetts, New Jersey, North Carolina, Pennsylvania, Brazil, Canada, China, Ireland, Singapore, Switzerland, UK and four locations in India. Visit our website at www.ipsdb.com.

     

    Specialties

     

    Process Architecture, Process Design, Engineering, Construction, Commissioning, Qualification, LEAN Project Delivery, Strategic Master Planning, Energy Conservation Management, Project Controls, Program/Project Management, Operations/Logistics Strategy and Planning, EPCMV and Staffing Services.

     

    IPS is an equal opportunity, affirmative action employer of protected veterans (M/F/D/V).

     

    Attention Search Firms / Third Party Recruiters:  IPS is not seeking assistance or accepting unsolicited resumes from search firms for employment opportunities with IPS. Regardless of past practice, all resumes submitted by search firms to any employee at IPS via-email, the Internet or directly to hiring managers at IPS in any form without a valid written search agreement in place for a specific position will be deemed the sole property of IPS, and no fee will be paid in the event a candidate is hired by IPS as a result of the referral or through other means.

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