Equipment Commissioning & Qualification (ECQ) Engineer

ECLARO; Summit (NJ); On-site; USD 84,000 - 90,000; Full time

Benefits offered by this job

401k Retirement Savings Plan

Commuter Benefits

Medical/Dental/Vision Insurance

Job summary

ECLARO is seeking an Equipment Commissioning & Qualification (ECQ) Engineer for its client in Summit, NJ. The role focuses on commissioning, qualification and maintenance of equipment, facilities, and utilities in a GMP environment.

You will develop qualification protocols, supervise vendors, and support validation activities while adhering to regulatory requirements and company policies. Strong communication and multi-tasking are essential.

Qualifications

• Knowledge of cGMP, GXP, GAMP, SDLC regulations, including 21CFR part 11, computer systems validation requirements and good documentation practices.
• Understanding of GMP manufacturing and laboratory systems and CAPA management.
• Strong written and verbal communication skills and ability to handle multiple projects.
• Experience with Electronic Data Management Systems such as Valgenesis is preferred.
• Minimum of 5 years in a GMP environment and 3 years in equipment/utility qualification.

Responsibilities

• Commissioning and Qualification activities for equipment, facilities and utilities, including development of protocols and reports.
• Supervise vendors for qualification functions and support validation deliverables.
• Manage projects of limited scope, coordinating with internal customers and external service providers.
• Provide technical support on qualification issues and ensure regulatory compliance.
• Maintain strict adherence to change management and documentation practices.

Skills

cGMP knowledge

Regulatory knowledge

Communication skills

Multitasking

Team collaboration

Computer literacy

Quality focus

Education

BS in Engineering or Science

Tools

Valgenesis

Job description

Job Number: 26-01335Be part of a company that delivers life-changing healthcare solutions. ECLARO is looking for an

Summit, NJ.ECLARO’s client is a leader in the Biopharmaceutical Industry, providing quality, innovative, and affordable medicines that make a difference in the lives of patients all over the world. If you’re up to the challenge, then take a chance at this rewarding opportunity!

Job Number: 26-01335Be part of a company that delivers life-changing healthcare solutions. ECLARO is looking for an Equipment Commissioning & Qualification (ECQ) Engineer for our client in Summit, NJ.ECLARO’s client is a leader in the Biopharmaceutical Industry, providing quality, innovative, and affordable medicines that make a difference in the lives of patients all over the world. If you’re up to the challenge, then take a chance at this rewarding opportunity!

Position Overview

• The Engineer, Equipment Commissioning & Qualification (ECQ) Delivery supports the successful implementation of equipment / instruments, facilities, and utilities, at multi-use sites through interaction with internal customers and external service providers.
• The person in this role is responsible for commissioning, qualifying and / or maintaining equipment / instruments, facilities, and utilities, in a commissioned / qualified / validated state according to established policies and procedures. 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.
• This role will require management of outside resources, and their own workload.
• As a developing team player, the person in this role 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.
• Reporting Relationship Manager or Senior Manager

Responsibilities

• Commissioning and Qualification Activities:
  • Maintain commissioned / qualified equipment, facilities, and utilities in compliance with policies, guidelines, and procedures:
  • Develop commissioning / qualification protocols, and associated reports while adhering to a change management process.
  • Supervise vendors for qualification functions.
  • Support development of equipment operational procedures.
  • Support all equipment validation activities. Execute equipment qualifications and validation protocols.
  • Develop validation / qualification deliverables such as Validation Plans, Requirements Specifications, Design Specifications, Traceability Matrices, and Summary Reports.
  • Support Change Management process.
• Project Work Support:
  • Manage projects of limited scope and complexity within their functional area:
  • Support equipment implementation projects including scheduling, site prep, installation, qualification, and turnover to business area.
  • Support internal customer groups in the operation, calibration, and preventive maintenance of equipment to meet business needs in accordance with required schedules or dates.
  • Complete all qualification and validation documentation with accuracy, completeness, and compliance to Client standards.
• Customer Service and Support:
  • Regularly review, prioritize, and promptly respond to customer equipment qualification and support requests.
  • Provide technical support and guidance on equipment qualification issues. Interfaces with customers to ensure all expectations are being met.
  • Provide technical support and guidance on equipment, utilities, facilities, and computerized systems qualification and validations issues.
  • Maintain 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 participate in deviation investigations as an SME.

Qualifications

• Knowledge of cGMP, GXP, GAMP, SDLC regulations, including 21CFR part 11, computer systems validation requirements and good documentation practices.
• Knowledge of pharmaceutical, manufacturing and laboratory systems.
• Understanding of investigations, deviations and CAPA management in a 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.
• Detail-oriented with strong commitment to quality, safety, and compliance.
• Ability to effectively manage multiple projects simultaneously and prioritize tasks effectively.
• Highly proficient computer skills in Microsoft Office Suite - Word, Excel, PowerPoint, and Outlook with extensive background in database systems. Innate ability to learn new software, such as corporate intranet and enterprise business tools.
• Experience with Electronic Data Management Systems such as Valgenesis, preferred.
• BS in Engineering or Science related discipline preferred but can be substituted with sufficient relevant experience.
• Minimum of 5 years of experience performing / supporting activities in a GMP environment.
• Minimum of 3 years of experience in equipment, facilities, or utilities qualification.

Pay Rate: $61.95 - $65.70 / Hour

If hired, you will enjoy the following ECLARO Benefits:

• 401k Retirement Savings Plan administered by Merrill Lynch
• Commuter Check Pretax Commuter Benefits
• Eligibility to purchase Medical, Dental & Vision Insurance through ECLARO

Equal Opportunity Employer: ECLARO values diversity and does not discriminate based on Race, Color, Religion, Sex, Sexual Orientation, National Origin, Age, Genetic Information, Disability, Protected Veteran Status, or any other legally protected group status, in compliance with all applicable laws.