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LL01-251008 Engineering Technical Lead

Department: Field - LL
Location: Thousand Oaks, CA

Validation & Engineering Group, Inc. (V&EG) 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 Lead

The Engineering Technical Lead for Packaging Lines will provide technical leadership, oversight, and subject-matter expertise for the design, installation, commissioning, qualification, and lifecycle support of packaging systems at a state-of-the-art biotechnology facility.
This role bridges project engineering, automation, validation, and operations, ensuring that packaging processes meet GMP/FDA regulatory requirements, corporate engineering standards, sustainability goals (LEED v4), and business needs for quality, cost, and schedule.


Key Responsibilities:

Project Leadership & Delivery

  • Serve as the primary technical lead for all packaging line engineering activities across capital projects and site initiatives.
  • Oversee URS/BOD/Design Review development for vial, syringe, and/or combination-product packaging lines (e.g., filling, labeling, cartoning, serialization, aggregation, palletizing).
  • Coordinate vendor selection, FAT/SAT, IOQ/PQ readiness, and integration with upstream manufacturing, utilities, and warehouse systems.
  • Ensure packaging equipment design and installation comply with cGMP, GAMP 5, corporate engineering standards, and safety/ergonomic guidelines.

Commissioning & Qualification

  • Lead cross-functional teams to execute Cx/Qx protocols for equipment, utilities, and automated control systems, ensuring full 21 CFR Part 11 compliance.
  • Support resolution of punch-list items, deviations, and CAPAs during start-up and ramp-up phases.
  • Oversee the development of SOPs, maintenance plans, and spare-parts strategies for packaging assets.

Technical Support & Continuous Improvement

  • Provide technical troubleshooting for equipment reliability, product quality, and automation interfaces (e.g., SCADA/BAS/MES, serialization systems).
  • Drive OEE improvements, line balancing, and changeover optimization to support high-volume biotech packaging operations.
  • Champion sustainability and energy-efficient design of packaging areas, aligned with LEED v4 energy & atmosphere credits.
  • Ensure robust data integrity, safety, and regulatory compliance throughout the equipment lifecycle.

Team & Stakeholder Engagement

  • Act as the primary liaison among Engineering, Validation, Automation, EHS, Quality, Manufacturing, and external suppliers.
  • Mentor junior engineers and collaborate with Cx Agents/Consultants, Validation Leads, and Reliability teams to ensure knowledge transfer and operational readiness.
  • Communicate project updates, risk assessments, and mitigation plans to site and global leadership.

Qualifications:

Required:

  • Bachelor’s degree in Mechanical, Electrical, Chemical, or Industrial Engineering (Master’s preferred).
  • 8+ years of engineering experience in pharmaceutical/biotech packaging lines, including installation and startup of automated filling, labeling, and cartoning equipment.
  • Strong knowledge of GMP, FDA/EMA regulations, ISO 13485 (for combination products), serialization/aggregation, and GAMP 5 automation standards.
  • Demonstrated success leading multidisciplinary project teams through design, construction, and qualification phases.
  • Proficiency in MS Project/Primavera, technical drawing review (AutoCAD/Revit), and common plant utilities.

Preferred:

  • Familiarity with BAS/MES/serialization platforms (e.g., PAS-X, Rockwell, Siemens, Systech, Antares).
  • Excellent problem-solving, communication, and vendor-management skills.
  • Lean Six Sigma Green Belt or equivalent continuous improvement training.

Core Competencies:

  • Technical Leadership & Decision-Making
  • GMP Compliance & Documentation Rigor
  • Cross-Functional Teamwork & Vendor Coordination
  • Problem Solving under Tight Timelines
  • Commitment to Safety, Quality, and Sustainability

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