Computerized Systems Validation Analyst

5 days ago


New Delhi, India Innovaderm Research Full time

The role of the CSV is to establish quality validation packages for the GxP computerized systems used at Innovaderm with the goal of ensuring data integrity and compliance with the regulatory and industry requirements.


More specifically, CSV Analyst:

  • Establishes computerized system validation schedule for key deliverables with the system owners and functional departments.
  • Determines the extent of system validation based on the policy, standard operating procedures (SOPs), system type and risk-assessment.
  • Leads the development and/or review of the validation packages including but not limited to Validation Plan, user requirement specification (URS), ERES Assessment, System risk assessment, functional and configuration specifications, test scripts (IQ/OQ/PQ), data migration verification, traceability matrix, validation summary report.
  • Assesses the completeness of vendor validation packages to determine if it can be leveraged to support validation of computerized systems at Innovaderm.
  • Leads post-implementation validation activities for the lifecycle of GxP Computerized systems (including but not limited to Change Control Management, CAPA, Periodic Review, Internal and External Audit Support, Verification of Data Migration/Data Back up/Archival, System Retirement)
  • Provide support and guidance to the system owners/system administrators for their responsibilities for the management of computerized systems (e.g., periodic review).
  • Can participate to the establishment/review of SOPs and process improvement initiatives.
  • Contribute to training content related to the computerized systems aspects.
  • Provides solutions to a wide range of problems through individual efforts in a creative, thorough, practical, and consistent fashion in line with applicable regulations
  • Provides support, if required, to QA team during vendor qualification, internal and external audit processes.


Our company:

OUR COMPANY

 

The work environment

At Innovaderm, you will work with brilliant and driven colleagues. Our values are collaboration, innovation, reliability, and responsiveness. We offer a stimulating work environment and attractive advancement opportunities. 

 

In this position, you will be eligible for the following perks: 

  • Flexible schedule
  • Vacation
  • Home-based position
  • Ongoing learning and development


Work location

Note that this opening is for a home-based position in India. 


About Innovaderm

Innovaderm is a contract research organization (CRO) specialized in dermatology. Since its beginnings in 2000, our organization has benefited from a solid reputation for the quality of its research and services exceeding the expectations of its clients. Based in Montreal, Innovaderm continues to grow and expand in North America and Europe.

 

Innovaderm is committed to providing equitable treatment and equal opportunity to all individuals. As such, Innovaderm will provide accommodations throughout the recruitment and selection process to applicants with disabilities, upon request.

Innovaderm only accepts applicants who can legally work in India. 


IDEAL PROFILE


Education 

  • Bachelor’s degree in computer science, engineering life science or related field.
  • Equivalent experience and/or will be also considered.


Experience

  • Minimum of 5 years of experience in Computerized Systems validation in the GxP industry; prior experience with clinical platforms is an asset (e.g., IWRS, EDC, ePRO/eCOA, eConsent).


Knowledge and skills

  • Excellent knowledge of regulations and guidelines related to computerized systems validation (US FDA 21 CFR part11, EU annexe 11, Health Canada, GDPR, ICH.
  • Strong technical knowledge to provide concise and clear documentation, verbal communication, interpersonal and problem-solving skills.
  • Ability to work independently.
  • Good knowledge of the Microsoft Office Suite (Word, Excel, PowerPoint) and other tools used in CSV (e.g., JIRA, HPALM, DMS).
  • Good organization skills and ability to adapt to a rapidly growing environment.
  • English, written and spoken.
  • Experience in writing & reviewing SOPs for accuracy and GxP compliance.
  • Organizational abilities to meet accelerated timelines, manage multiple shifting priorities and maximize efficiencies in a dynamic customer-focused environment.
  • Superior attention to details.
  • Critical-thinking and problem-solving skills; ability to recognize and resolve discrepancies and issues.


  • new delhi, India Innovaderm Research Full time

    The role of the CSV is to establish quality validation packages for the GxP computerized systems used at Innovaderm with the goal of ensuring data integrity and compliance with the regulatory and industry requirements. More specifically, CSV Analyst: Establishes computerized system validation schedule for key deliverables with the system owners and...


  • New Delhi, India Innovaderm Research Full time

    The role of the CSV is to establish quality validation packages for the GxP computerized systems used at Innovaderm with the goal of ensuring data integrity and compliance with the regulatory and industry requirements.More specifically, CSV Analyst:Establishes computerized system validation schedule for key deliverables with the system owners and functional...


  • Delhi, India PSC Biotech Full time

    Job DescriptionPSC Biotech provides the life sciences with essential services to ensure that health care products are developed, manufactured, and distributed to the highest standards, in compliance with all applicable regulatory requirements.Our goal is to skyrocket our clients’ success, and you can be a part of our team’s achievements. Employing a...

  • Validation Engineer

    4 weeks ago


    Delhi, India PQE Group Full time

    We are looking to hire aCSV Consultantfor a full-time role forChennai locationto join our growing team.Scope of Work (Computer Software Validation)Execute qualification and validation activities of all pharmaceutical laboratory equipment’s.Execute System audit trail and user management periodic review.Responsible to co-ordinate with vendors for...

  • Validation Engineer

    4 weeks ago


    delhi, India PQE Group Full time

    We are looking to hire a CSV Consultant for a full-time role for Chennai location to join our growing team.Scope of Work (Computer Software Validation)Execute qualification and validation activities of all pharmaceutical laboratory equipment’s.Execute System audit trail and user management periodic review.Responsible to co-ordinate with vendors for...

  • Validation Engineer

    2 weeks ago


    Delhi, Delhi, India PQE Group Full time

    We are looking to hire aCSV Consultantfor a full-time role forChennai locationto join our growing team.Scope of Work (Computer Software Validation)Execute qualification and validation activities of all pharmaceutical laboratory equipment's.Execute System audit trail and user management periodic review.Responsible to co-ordinate with vendors for...

  • Validation Engineer

    2 weeks ago


    Delhi, Delhi, India PQE Group Full time

    We are looking to hire a CSV Consultant for a full-time role for Chennai location to join our growing team.Scope of Work (Computer Software Validation)Execute qualification and validation activities of all pharmaceutical laboratory equipment's.Execute System audit trail and user management periodic review.Responsible to co-ordinate with vendors for...


  • delhi, India SUN PHARMA Full time

    Job Responsibilities:Perform review of Computerized System Validation of IT systems of Manufacturing SitesSupport various phases of Computer System including Planning, Implementation, Maintenance and retirement activities by ensuring compliance with internal / external regulatory requirementsPerform GxP computerized systems assessment referring requirement...

  • Validation Engineer

    3 weeks ago


    Delhi, India PSC Biotech Full time

    Job DescriptionPSC Biotech provides the life sciences with essential services to ensure that health care products are developed, manufactured, and distributed to the highest standards, in compliance with all applicable regulatory requirements.Our goal is to skyrocket our clients’ success, and you can be a part of our team’s achievements. Employing a...

  • HW System Validation

    3 weeks ago


    Delhi, India Global Pharma Tek Full time

    Job Description:DSP Verification & Validation within Bangalore Design Center is responsible for verifying and validating hardware solutions and to integrate new hardware (IP cores and SoCs) to maximize software productivity and enable faster time to market. This organization is central to minimizing the number of chip turns in products, to the efficient...

  • CSV Specialist

    2 days ago


    Delhi, India Entiovi Technologies Full time

    COMPUTERIZED SYSTEM VALIDATION (CSV) SPECIALIST JDLocation:Onsite/Offshore (Relocation assistance available for candidates willing to move to Germany)Company Overview:We atEntiovi Technologies , provide digital transformation using new-age intelligent technologies formore than 7 years . We have clients located primarily in the US and Europe thatare served by...

  • HW System Validation

    2 weeks ago


    Delhi, Delhi, India Global Pharma Tek Full time

    Job Description:DSP Verification & Validation within Bangalore Design Center is responsible for verifying and validating hardware solutions and to integrate new hardware (IP cores and SoCs) to maximize software productivity and enable faster time to market. This organization is central to minimizing the number of chip turns in products, to the efficient...

  • Validation Engineer

    2 weeks ago


    Delhi, Delhi, India PSC Biotech Full time

    Job DescriptionPSC Biotech provides the life sciences with essential services to ensure that health care products are developed, manufactured, and distributed to the highest standards, in compliance with all applicable regulatory requirements.Our goal is to skyrocket our clients' success, and you can be a part of our team's achievements. Employing a global...


  • Delhi, Delhi, India Chara Technologies Full time

    At Chara Technologies ) we are building revolutionary cloud-connectedelectric motors for scalable deployment in various applications ranging from Electric Vehicles toUnmanned Aerial Vehicles. We design and develop the hardware and software that drives thesemotors. The founders are veteran serial entrepreneurs, product experts, and motor technologists...


  • Delhi, India Vaisesika Full time

    Vaisesikais looking for Computer System Validation profiles.Experience : 6+ yearsNotice : ImmediateLocation : RemoteKey Responsibilities:Should have 4+ years of experience in computer system validation in the life sciences domain.Strong understanding of regulatory requirements, including FDA 21 CFR Part 11, EU Annex 11 and GAMP5.Proficiency in validation...


  • delhi, India Vaisesika Full time

    Vaisesika is looking for Computer System Validation profiles.Experience : 6+ yearsNotice : ImmediateLocation : RemoteKey Responsibilities:Should have 4+ years of experience in computer system validation in the life sciences domain.Strong understanding of regulatory requirements, including FDA 21 CFR Part 11, EU Annex 11 and GAMP5.Proficiency in validation...


  • Delhi, Delhi, India PSC Biotech Full time

    Job DescriptionThe Computer Systems Validation Engineer (CSV) will be responsible for assisting in planning, writing, implementing, and reviewing validation protocols for computer-based systems. The person is responsible for making sure computer-based systems are operating as intended and meet regulatory requirements. The incumbent is also responsible and...


  • Delhi, Delhi, India Instrumentation & Control Solutions Full time

    A CSV consultant will use his/her knowledge of FDA cGMP and related regulations and guidelines, and specific knowledge of computer validation methodologies and principles to perform CSV on a variety of systems and programs. Experience of QA in a FDA regulated environment is preferred.At least 2 years of Computer System Validation or any validation experience...

  • Validation Engineer

    1 month ago


    New Delhi, India IPS-Integrated Project Services Full time

    Looking for a candidate with Good Knowledge in Bio-Pharmaceutical manufacturing Processes and the Process equipment for OSD/Sterile/Creams/Ointment manufacturing, API manufacturing/High Potent compound manufacturing (Product/Personnel/facility Containment requirement) and facility design requirement.Should be able to conduct Quality Audits, Gap Analysis of...


  • New Delhi, India Kimbal Technologies (formerly Crystal) Full time

    As a Validation engineer, you will be the key person to conduct FAT, SAT, POCs and other tests in line with RFP/SBD requirements under smart metering projects in front of the customer, utilities and consultants. This position is customer facing and, in this position, you will be fully accountable for the success of the FATs, SATs and POCs. Following are the...