Sr. Process Engineer

Syner-G • Middletown, VA

1d • Remote

About The Position

A career here is life-enhancing. At Syner-G, we enable our people to build careers that impact positively on their quality of life. Through our expertise, insight, consulting and management skills, we accelerate breakthrough science and delivery of life-enhancing therapies to more patients. We work across a diverse range of clients and projects, supporting many organizations from the most critical phases of the drug discovery and approval process through to commercialization. It is meaningful, varied and thought-provoking work with a strategic emphasis, a solutions-driven approach and significant, real-world outcomes, from science to delivery/success. Underpinning this mission is a culture that aligns perfectly with what we want to achieve. We enable our people to grow, we support them in their learning and we reward them in so many different ways. In return, they play an instrumental role in maintaining our reputation across the globe as a strategic biopharma product development and delivery partner. Syner-G was recently honored with BioSpace's prestigious "Best Places to Work" 2026 award, for the third consecutive year, along with many other award-winning programs to make a career here truly life-enhancing. These recognitions are a testament to our commitment to fostering a positive and engaging work environment for our employees, with a particular emphasis on culture, career growth and development opportunities, financial rewards, leadership and innovation. At Syner-G, we recognize that our team members are our most valuable asset. Join us in shaping the future, where your talents are valued, and your contributions make a meaningful impact. For more information, visit www.Synergbiopharma.com We are seeking a Sr. Process Engineer with a strong background in mechanical or manufacturing engineering and hands-on experience in automated manufacturing environments, preferably within the life sciences or biopharma industry. The ideal candidate will have demonstrated expertise in line layouts, fixture design, 3D printing, and project management, with a preference for experience in high-speed fill-finish lines and filling and capping equipment (though not essential). Familiarity with PLCs and HMIs is required, though this is not a controls engineering role. Proficiency in AutoCAD and SolidWorks is essential. Travel to client sites may be required up to 100%, based on project demands and client expectations.

Requirements

• Bachelor’s degree in Mechanical Engineering, Manufacturing Engineering, or a related technical field
• 4 to 7 years of engineering experience in automated manufacturing, preferably in life sciences or biopharma
• Proficient in AutoCAD and SolidWorks
• Familiarity with PLCs and HMIs
• Experience with cGMP manufacturing in FDA-regulated environments
• Knowledge of cGxP quality systems and applicable regulatory standards
• Proficient in MS Office, MS Project, and Visio
• Strong project management and cross-functional communication skills
• Innovative problem-solving and technical analysis capabilities
• Ability to work hands-on in a fast-paced, regulated environment
• Willingness to travel to client sites as needed

Nice To Haves

• Experience with high-speed fill-finish lines and filling/capping equipment is a plus

Responsibilities

• Lead and support process engineering activities including design, development, and optimization of automated manufacturing systems
• Develop and implement line layouts and custom fixtures to support manufacturing efficiency and scalability
• Apply 3D printing technologies for prototyping and fixture development
• Manage small to mid-sized engineering projects, ensuring cross-functional collaboration and effective communication
• Support commissioning and qualification of facilities, utilities, and equipment
• Assist with technology transfer, process development, and validation activities
• Conduct risk assessments and feasibility reviews to ensure compliance with manufacturing and regulatory requirements
• Provide technical support for lifecycle management, scale-up, and continuous improvement initiatives
• Collaborate with vendors and third-party contractors to support project execution and process optimization
• Ensure adherence to cGMP, FDA regulations, and industry standards

Benefits

• We define total rewards as compensation, benefits, remote work/flexibility, development, recognition, and our culture with programs that support each of our reward pillars.
• This includes a market competitive base salary and annual incentive plan, robust benefit offerings, and ongoing recognition and career development opportunities.
• Employees also enjoy our generous flexible paid time off program, company-paid holidays, flexible working hours, and fully remote work options for most positions and the ability to work “almost anywhere.”
• However, if a physical work location is more for you, we have office locations in Greater Boston; San Diego, CA; Boulder, CO; and India.

What This Job Offers

• Job Type: Full-time
• Career Level: Mid Level