Equipment Commissioning & Qualification; ECQ) Engineer
Job in
Summit, Union County, New Jersey, 07901, USA
Listed on 2026-09-02
Listing for:
ECLARO
Full Time
position Listed on 2026-09-02
Job specializations:
-
Engineering
Validation Engineer, Pharma Engineer, Quality Engineering, Biomedical Engineer
Job Description & How to Apply Below
Equipment Commissioning & Qualification (ECQ) Engineer
Be 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.
- Maintain commissioned / qualified equipment, facilities, and utilities in compliance with policies, guidelines, and procedures:
- 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.
- Manage projects of limited scope and complexity within their functional area:
- 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 21
CFR 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…
To View & Apply for jobs on this site that accept applications from your location or country, tap the button below to make a Search.
(If this job is in fact in your jurisdiction, then you may be using a Proxy or VPN to access this site, and to progress further, you should change your connectivity to another mobile device or PC).
(If this job is in fact in your jurisdiction, then you may be using a Proxy or VPN to access this site, and to progress further, you should change your connectivity to another mobile device or PC).
Search for further Jobs Here:
×