Engineering Technical Leads ETL

Posted 2 Days Ago
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Juncos, PRI
In-Office
Senior level
Biotech • Consulting • Pharmaceutical • Manufacturing
The Role
Lead ETL engineering activities for pharmaceutical/biotech projects including design planning, standards compliance, vendor liaison, RFIs/submittals, change management, FAT planning, design qualification reports, and support for commissioning and site change control. Ensure cGxP, EHSS, and Factory Mutual considerations are integrated and track design progress against project schedules.
Summary Generated by Built In

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.

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

  • Engineering Technical Leads ETLs

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

Provide ETL Support Services to support the project

  • 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.

Excited to build something meaningful together? We look forward to hearing from you.

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.

#LI-ZL1

Skills Required

  • Bachelor's Degree in Science or Engineering
  • Minimum of 5 years experience in pharmaceutical, medical device, or biotechnology industries
  • Fully bilingual English/Spanish with excellent oral skills
  • Strong knowledge of cGxP and regulatory guidance and their application to compliance
  • Technical writing skills and investigation processes
  • Available to work extended hours, including possible weekends and holidays
  • Experience with e-Builder (preferred)
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The Company
154 Employees
Year Founded: 2019

What We Do

Pinnaql, Inc. is a professional services consulting firm providing quality, regulatory, and operational excellence solutions to biopharmaceutical, medical device, and CDMO companies worldwide. The company specializes in laboratory validation, engineering, and compliance, helping regulated life sciences organizations navigate manufacturing challenges, reduce execution risks, and accelerate the transition from lab innovation to commercial market readiness.

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