Engineering Technical Leads ETL

Pinnaql; Caguas (PR); On-site; USD 80,000 - 100,000; Full time

Job summary

Pinnaql is seeking an Engineering Technical Lead in Caguas, Puerto Rico. This role involves providing ETL support services, leading the design process, and ensuring compliance with engineering standards. The ideal candidate has a Bachelor's Degree in Science or Engineering, along with 5 years of experience in pharmaceutical, medical device, or biotechnology fields. Strong bilingual communication skills in English and Spanish are essential. Join a purpose-driven team to shape the future of healthcare and technology.

Qualifications

• 5+ years of experience in the pharmaceutical, medical device, or biotechnology industries.
• Strong understanding of regulatory compliance.
• Available for extended hours, weekends, and holidays.

Responsibilities

• Provide ETL support services and lead the design process.
• Review project plans for adherence to engineering standards.
• Act as a liaison to engineering authorities and equipment vendors.

Skills

Bilingual (English / Spanish)

Technical Writing

Knowledge of cGxP

Problem-solving skills

Education

Bachelor's Degree in Science or Engineering

Job description

Validation & Engineering Group, Inc. (V&EG) a Pinnaql company is a leading services supplier who provides solutions for the Pharmaceutical, Biotechnology, Chemical, Food, and Medical Devices industries in the following areas: Laboratory, Compliance, Computer, Engineering, Project Management, Validation, and other services.

Engineering Technical Leads ETLs

We are seeking a talented, dedicated individual committed to work under the highest ethics standards for the following position.

Project Scope

• Provide ETL Support Services.
• Preparation of front-end planning documents.
• Lead the design process.
• Provide value engineering / creative problem solving.
• Participation in the development of the sourcing strategy for projects.
• Evaluate the design library against the project scope and issue relevant specifications or standards.
• Review of the projects plans for adherence to Amgen engineering standards and specifications.
• Identification of possible deviations to the site specifications. Submittal and approval of variance.
• Ensure Factory Mutual loss prevention recommendations are issued and addressed in the design.
• Ensure EHSS requirements are considered in the design.
• Technical support during project execution and lead for discrepancies.
• Liaison to engineering technical authorities, subject matter experts, consultants, and engineer of record.
• RFI and submittal review process.
• Track design progress against plan and ensure alignment with overall project’s schedule.
• Engineering change management.
• Consultant to site commissioning and qualification work stream.
• Consultant to site change control evaluation process.
• Point of contact between equipment vendors and the site.
• Establish method to manage information and documents. e-Builder preferred for capital projects.
• Factory acceptance test planning.
• Ensure project plans and details are fit to introduce equipment.
• Develop, submit, and approve design qualification report (for level 1 systems), and DDR for level 2 and 3.

Delivery Criteria

• Scope of facilities
• Project requirements
• Design Plan
• Design review reports
• Design qualification report
• Conceptual design documents
• e-Builder processes
• Submittals
• RFIs
• Turnover packages
• Engineering Change Notices
• Other Activities
• Field visits to confirm existing documentation and installations.

Qualifications

• Bachelor's Degree in Science or Engineering.
• Minimum of 5 years of experience in direct pharmaceutical, medical device or biotechnology industries.
• Must be fully bilingual (English / Spanish) with excellent oral skills.
• Strong knowledge in cGxP and regulatory guidance as well as understanding of how they are applied to regulatory compliance.
• Technical Writing skills and investigations processes.
• Available to work extended hours, possibility of weekends and holidays.

At Validation & Engineering Group, people always come first. We believe that when you're empowered to do your best work, bold ideas thrive and real progress happens. This isn't just a job - it's an opportunity to make a meaningful difference by shaping the future of healthcare and technology alongside a purpose-driven, supportive team.

Validation & Engineering Group is an equal opportunity employer. All applicants will be considered for employment without regard to race, color, religion, sex, sexual orientation, gender identity, national origin, veteran status, or disability status.