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Manufacturing & Tech Ops - Lead Engineer - Project Farma

Job in Bethesda, Montgomery County, Maryland, 20811, USA
Listing for: PerkinElmer
Full Time position
Listed on 2026-08-13
Job specializations:
  • Quality Assurance - QA/QC
    Quality Engineering
Salary/Wage Range or Industry Benchmark: 99000 - 122000 USD Yearly USD 99000.00 122000.00 YEAR
Job Description & How to Apply Below

When joining Perkin Elmer, you select an experienced and trusted leader in scientific solutions, with the support of a global service network and distribution centers, providing the right solution, at the right time, to meet critical customer needs. With over an 80+ year legacy of advancing science and a mission of innovating for a healthier world, our dedicated team collaborates closely with commercial, government, academic and healthcare customers to deliver our broad portfolio of analytical solutions, and One Source services.

Job

Title

Manufacturing & Tech Ops
- Lead Engineer
- Project Farma

Location(s)

Customer Site - MD

Job Description

This is a full‑time salaried position with Project Farma, a Perkin Elmer company. The successful candidate will reside in Maryland and be willing to travel domestically to meet client project requests. Project Farma’s purpose is to improve patient lives by accelerating the delivery of life‑changing therapies. We accomplish this through the successful execution of high‑quality life sciences projects across the full project lifecycle.

Project Farma (PF) team members collaborate with cross‑functional teams to build trusted client relationships, deliver an exceptional customer experience, and contribute to business growth by identifying opportunities and applying data‑driven insights to support project planning, cost, schedule, and performance management. This role contributes to organizational success by supporting financial performance, operational efficiency, and continuous improvement, while also investing in people through mentorship, knowledge sharing, and professional development.

All team members are expected to embody Project Farma’s values by being curious, personable, and unselfish, while maintaining a strong commitment to a Patient Focused and People First mindset. The Manufacturing & Tech Ops
- Lead Engineer is an advanced individual contributor with demonstrated depth in their technical discipline and a growing record of leading complex work streams. This role applies strong subject‑matter expertise to solve high‑impact technical and operational challenges, supports technical decision‑making, and contributes to the evolution of standards, methods, or best practices within their area. The Lead Engineer works with a high degree of independence, mentors junior and peer engineers, and partners closely with project and people leaders—while remaining focused on technical delivery rather than formal people management.

Key Responsibilities
  • Lead or Support end‑to‑end program management for complex technical operations initiatives including new product introductions, technology transfers, process validations, and facility fit assessments.
  • Develop integrated program plans, critical path analyses, risk registers, and resource plans; proactively identify and elevate risks and issues.
  • Contribute to the completion of stage‑gate processes and governance deliverables, ensuring milestones are met on time, within scope, and aligned to regulatory commitments.
  • Coordinate or work with cross‑functional work streams across Manufacturing, Process Development, Quality, Regulatory Affairs, Supply Chain, and Engineering.
  • Partner with technical subject matter experts to translate scientific and process requirements into executable operational plans, development of staff awareness of critical process parameters (CPP) and critical quality attributes (CQA).
  • Support technology transfer activities from development into GMP manufacturing, including documentation, gap assessments, and readiness reviews.
  • Facilitate resolution of technical, operational, and quality issues that arise during operations, startup or shutdown of manufacturing equipment.
  • Development of manufacturing batch records, SOPs or validation protocols As required..
  • Perform operational readiness assessments that fully evaluate equipment suitability and reliability, facility fit and finish, material workflow, supply chain planning, training materials and programs, quality and compliance, sampling plans, area risk assessments and personnel PPE/gowning requirements, cleaning procedures and frequency, tier communication plans,…
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