Process Engineer

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Val Source is currently looking to identify experienced and technically skilled leaders in Process/Process Equipment Engineering to support GMP Drug Substance and Drug Product capital projects throughout our network. This is a key part of strengthening Val Source's role in front-end Engineering and enabling end-to-end support for our clients.

Val Source is currently looking to identify experienced and technically skilled leaders in Process/Process Equipment Engineering to support exciting GMP Drug Substance and Drug Product capital projects throughout our network. This is a key part of strengthening Val Source's role in front-end Engineering and enabling end-to-end support for our clients.

• Reporting to the client’s Process Engineering or Area Manager, while demonstrating independent drive and sound judgment in day-to-day operations at the client site.
• Collaborating closely with client teams and internal staff to act in the best interest of the client.
• Lead the project through an offsite design effort (at the Design partner’s location), to onsite installation and execution at the Client site.
• Manage multidisciplinary teams with representatives from Process Engineering, Automation, Commissioning, Qualification & Validation (CQV) and others to drive projects through capital management phases from Concept Design, through Detailed Design and Execution.
• Provide clear technical leadership and expertise to lead teams through Safety assessments (PHA, HAZOP and LOPA) and Quality assessments (Development of CIP/SIP strategy, Automation development and GMP Design review). Gather internal and external stakeholder requirements and communicate clear owner’s intent, ensure stakeholders are aligned or if not, escalate issues for rapid decision making.
• Collaborate strongly with client Subject Matter Experts (SMEs) for critical design decisions.
• Demonstrate strong organization, technical writing and communication skills. Coordinate succinctly and effectively with the management and reporting team to drive clear and timely decision making.
• Manage quality, schedule and cost within prescribed project limits.

• Lead and oversee Owner’s Representatives activities for process areas and equipment.
• Lead and manage process scope across Compounding/Formulation, Component and Stopper Preparation, Syringe Filling Equipment, Automated Visual Inspection Systems, Autoinjector Assembly Equipment, and Secondary Packaging Lines.

• Lead cross-functional teams across engineering, quality, validation, and operations.
• Collaborate with project teams and internal stakeholders to ensure alignment of design, installation, and qualification with Owner’s requirements.
• Bring in internal SMEs as needed to address specialized technical issues.

• Proactively gather and clarify stakeholder requirements.
• Clearly communicate Owner’s intent to project teams.
• Facilitate alignment across disciplines; escalate unresolved issues for timely resolution.

• Ensure all assigned equipment areas meet project safety, quality, schedule, and cost targets.
• Drive results—anticipate challenges, resolve issues independently, and ensure discipline deliverables are achieved in full, on time, and on budget.
• Take ownership and accountability for area performance through all project phases.

• Bachelor’s degree in engineering or related field.
• Minimum of 6-8+ years of experience in pharmaceutical or biotech manufacturing projects.
• Strong working knowledge of GMP systems, equipment qualification, and process operations.
• Proven ability to lead teams, manage stakeholders, and drive performance across disciplines.
• Excellent communication, problem-solving, and organizational skills.
• Willingness to travel and spend time at both Conshohocken and Holly Springs locations.

This is a full-time position with Val Source. We are not considering applications from employment agencies, independent contractors, or third-party vendors. In compliance with federal…