Artech LLC
Engineering - Validation Engineer Validation Engineer
Artech LLC, Summit, New Jersey, us, 07902
Title:
Engineering - Validation EngineerJob Duration:
12+ Months (possible extensions)Job Location:
Summit, NJJob Description:
50% onsite requiredWork schedule:
M-F (Should be flexible on timings based on business needs)Purpose and Scope of Position:
The CSV Engineer supports the successful implementation of manufacturing and laboratory equipment, and computerized systems at multi-use sites through interaction with internal customers and external service providers. The incumbent in this role contributes to the completion of milestones associated with equipment qualification and systems validation. With minimum supervision and given general instructions, this individual carries out routine tasks and functions, and uses basic analytical skills to recognize and solve common problems of limited scope. As a developing team player, the incumbent interacts with their immediate supervisor and personnel within their own work group to achieve team goals while building trust and collaborative relationships outside the immediate organization.Required Competencies:
Knowledge, Skills, and Abilities:
Strong working knowledge of MS Windows client and server technologies.Working knowledge of standard networking principles and technologies.Excellent understanding of cGXP requirements and good documentation practices relating to systems, equipment, and instrumentation within the pharmaceutical industry.Strong working knowledge of ISPE guidance and 21 CFR Part 11 compliance.Ability to work with the end user to identify and document User and Functional Requirements.Knowledge of pharmaceutical laboratory and manufacturing systems.Experience executing equipment qualification documents.Ability to interact effectively with laboratory, QA, and Facilities groups.Strong ability to organize assigned tasks in a high-paced environment and concurrently monitor tasks/assignments with others that may impact timely completion. Ability to effectively manage multiple tasks and activities simultaneously.Strong written and verbal communication skills along with solid presentation skills. Proficient at writing well-formulated emails and reports. Ability to follow oral and written instructions, read and interpret engineering manuals/drawings relevant to the assigned task. Ability to effectively communicate with employees, contractors, and vendors. Experience with technical writing and document development/generation.Strong computer skills in Client Office Suite Word, Excel, Visio, and Outlook, and the ability to learn new software as required for equipment qualification.Competencies:
Technical / Professional KnowledgeProblem Solving / TroubleshootingAction OrientedAttention to DetailMulti-taskingBuilding RelationshipsEducation and Experience:
Required BS degree in Engineering / Computer ScienceMinimum 5 years of experience in FDA-regulated industry, with min 3 years experience in CSVDuties and Responsibilities:
Essential Functions:
Maintains all qualified and validated equipment and systems in compliance with policies, guidelines, and procedures.Develops protocols, and associated reports while adhering to a change management process.Supports the execution of equipment qualifications and validation protocols.Supervises vendors for qualification functions.Supports calibration, equipment qualification, and validation activities.Configures and documents the configuration of computerized systems.Develops validation/qualification deliverables such as Validation Plans, Requirements Specifications, Traceability Matrices, Summary Reports, and Change Controls.Manages projects of varying scope and complexity.Supports laboratory and manufacturing equipment implementation projects including scheduling, procurement, site prep, installation, qualification, and turnover to business area.Independent ownership of all lifecycle deliverables in the Qualification of equipment and full CSV for single and multi-user Computerized Systems.Supports internal customer groups in the procurement, operation, calibration, and preventive maintenance of equipment to meet business needs in accordance with required schedules or dates.Completes all qualification and validation documentation with accuracy, completeness, and compliance to Company standards.Provides excellent customer service and support.Regularly reviews, prioritizes, and promptly responds to customer equipment qualification and support requests.Provides technical support and guidance on calibration and equipment qualification issues. Interfaces with customers to ensure all expectations are being met.Maintains a positive relationship with all team members and site customers while promoting a positive team environment.Please E-MAIL your resume (attachment to email) with rate and availability to Aditya.
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Engineering - Validation EngineerJob Duration:
12+ Months (possible extensions)Job Location:
Summit, NJJob Description:
50% onsite requiredWork schedule:
M-F (Should be flexible on timings based on business needs)Purpose and Scope of Position:
The CSV Engineer supports the successful implementation of manufacturing and laboratory equipment, and computerized systems at multi-use sites through interaction with internal customers and external service providers. The incumbent in this role contributes to the completion of milestones associated with equipment qualification and systems validation. With minimum supervision and given general instructions, this individual carries out routine tasks and functions, and uses basic analytical skills to recognize and solve common problems of limited scope. As a developing team player, the incumbent interacts with their immediate supervisor and personnel within their own work group to achieve team goals while building trust and collaborative relationships outside the immediate organization.Required Competencies:
Knowledge, Skills, and Abilities:
Strong working knowledge of MS Windows client and server technologies.Working knowledge of standard networking principles and technologies.Excellent understanding of cGXP requirements and good documentation practices relating to systems, equipment, and instrumentation within the pharmaceutical industry.Strong working knowledge of ISPE guidance and 21 CFR Part 11 compliance.Ability to work with the end user to identify and document User and Functional Requirements.Knowledge of pharmaceutical laboratory and manufacturing systems.Experience executing equipment qualification documents.Ability to interact effectively with laboratory, QA, and Facilities groups.Strong ability to organize assigned tasks in a high-paced environment and concurrently monitor tasks/assignments with others that may impact timely completion. Ability to effectively manage multiple tasks and activities simultaneously.Strong written and verbal communication skills along with solid presentation skills. Proficient at writing well-formulated emails and reports. Ability to follow oral and written instructions, read and interpret engineering manuals/drawings relevant to the assigned task. Ability to effectively communicate with employees, contractors, and vendors. Experience with technical writing and document development/generation.Strong computer skills in Client Office Suite Word, Excel, Visio, and Outlook, and the ability to learn new software as required for equipment qualification.Competencies:
Technical / Professional KnowledgeProblem Solving / TroubleshootingAction OrientedAttention to DetailMulti-taskingBuilding RelationshipsEducation and Experience:
Required BS degree in Engineering / Computer ScienceMinimum 5 years of experience in FDA-regulated industry, with min 3 years experience in CSVDuties and Responsibilities:
Essential Functions:
Maintains all qualified and validated equipment and systems in compliance with policies, guidelines, and procedures.Develops protocols, and associated reports while adhering to a change management process.Supports the execution of equipment qualifications and validation protocols.Supervises vendors for qualification functions.Supports calibration, equipment qualification, and validation activities.Configures and documents the configuration of computerized systems.Develops validation/qualification deliverables such as Validation Plans, Requirements Specifications, Traceability Matrices, Summary Reports, and Change Controls.Manages projects of varying scope and complexity.Supports laboratory and manufacturing equipment implementation projects including scheduling, procurement, site prep, installation, qualification, and turnover to business area.Independent ownership of all lifecycle deliverables in the Qualification of equipment and full CSV for single and multi-user Computerized Systems.Supports internal customer groups in the procurement, operation, calibration, and preventive maintenance of equipment to meet business needs in accordance with required schedules or dates.Completes all qualification and validation documentation with accuracy, completeness, and compliance to Company standards.Provides excellent customer service and support.Regularly reviews, prioritizes, and promptly responds to customer equipment qualification and support requests.Provides technical support and guidance on calibration and equipment qualification issues. Interfaces with customers to ensure all expectations are being met.Maintains a positive relationship with all team members and site customers while promoting a positive team environment.Please E-MAIL your resume (attachment to email) with rate and availability to Aditya.
#J-18808-Ljbffr