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Manufacturing Systems Validation Specialist
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Manufacturing Systems Validation Specialist
1 month ago
Summit, United States Rangam Full timeMinimum 50% onsite required every week(Candidate is supposed to align the onsite days with manager and be available onsite when manager requests)The Specialist works cross-functionally to execute validation activities and prepare validation deliverables for S12 Enterprise Manufacturing Execution System (EMES) used in cell therapy manufacturing.This role is...
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Manufacturing Systems Validation Specialist
4 weeks ago
Summit, United States Rangam Full timeMinimum 50% onsite required every week(Candidate is supposed to align the onsite days with manager and be available onsite when manager requests)The Specialist works cross-functionally to execute validation activities and prepare validation deliverables for S12 Enterprise Manufacturing Execution System (EMES) used in cell therapy manufacturing.This role is...
Validation Engineer
2 months ago
Title:
Engineering - Validation Engineer
Location:
Summit NJ 07901
Duration:
6 months (High Possibility of extension for right candidate)
Job Description:
Purpose and scope of position:
The Equipment Validation Engineer supports the successful implementation of various process/lab equipment at multi-use sites through interaction with internal customers and external service providers.
The incumbent in this position is tasked with commissioning and qualifying new equipment facilities, and utilities and maintaining equipment systems in a qualified/validated state according to established policies and procedures.
The individual participates in projects and ongoing work activities of low to moderate complexity.
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 of cGMP, GXP, GAMP, and SDLC regulations, including 21CFR part 11, computer systems validation requirements, and good documentation practices.
Experience in the qualification of cell therapy equipment a plus.
Advanced knowledge of pharmaceutical, manufacturing, and laboratory systems.
Understanding of investigations, deviations, and CAPA management in the regulated pharmaceutical industry.
Strong written and verbal communication skills.
Excellent interpersonal skills with experience dealing with a diverse workforce.
Strong multi-tasking ability in conjunction with proven organizational skills. 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.
Highly proficient computer skills in Microsoft Office Suite - Word, Excel, PowerPoint, and Outlook with an extensive background in database systems. Innate ability to learn new software, such as corporate intranet and enterprise business.
Education and Experience:
BS in Engineering or Science related discipline required.
Minimum of 5 years' experience performing/supporting activities in a GMP environment.
Minimum of 3 years' experience in equipment, facility, or utility qualification.
Duties and responsibilities:
Maintains qualified equipment systems in compliance with policies, guidelines, and procedures:
Develops qualification 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.
Develops written procedures for calibration and preventive maintenance of equipment.
Supports equipment qualification and validation activities.
Develops validation/qualification deliverables such as Validation Plans, Requirements Specifications, Traceability Matrices, Summary Reports, Change Controls.
Manages projects of limited scope and complexity within their functional area:
Supports equipment implementation projects including scheduling, procurement, site prep, installation, qualification, and turnover to business area.
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 with Client 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 equipment qualification issues. Interfaces with customers to ensure all expectations are being met.
Provides technical support and guidance on equipment and computer systems qualification and validation issues.
Maintains a positive relationship with all team members and site customers while promoting a positive team environment.
Regulatory Responsibilities:
Ensure equipment, facilities, and programs are maintained in compliance.
May be called upon as SME in both internal and regulatory audits.
Working conditions (US only):
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:
Primarily office environment but will be required to enter laboratory or GMP process areas donning proper gowning/lab coats or PPE such as safety glasses and shoes.
Ability to work safely and effectively when working alone or working with others.
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