Syner-G · Plainville, Massachusetts, United States
Process Engineer
COMPANY DESCRIPTION: A career here is life-enhancing. At Syner-G, we enable our people to build careers that impact positively on their quality of life. Thro...
COMPANY DESCRIPTION:
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. To learn more about
who we are and what drives us, watch our company video here [https://www.youtube.com/watch?v=2rUMvtncuw8].
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 [https://www.synergbiopharma.com/]
POSITION OVERVIEW:
We are seeking an experienced Sr. Process Engineer to support the development and implementation of a comprehensive terminal
sterilization program. This individual will play a critical role in establishing the technical and operational framework for
sterilization processes that ensure product safety, regulatory compliance, and manufacturing readiness. The ideal candidate brings
deep technical expertise in terminal sterilization methods, strong program development experience, and the ability to collaborate
cross-functionally with CQV, engineering, and operations teams to design, implement, and execute robust sterilization solutions.
WORK LOCATION:
Travel to client sites may be required up to 100%, based on project demands and client expectations.
KEY RESPONSIBILITIES:
- Develop and document detailed sterilization process flow diagrams and program architecture
- Define sterilization recipes, cycle parameters, and operating ranges
- Establish overall sterilization program strategy, standards, and best practices
- Partner with CQV, engineering, and manufacturing teams to support execution and implementation
- Lead troubleshooting and technical problem-solving during cycle development and start-up
- Support commissioning, qualification, and validation activities (protocol development, execution support, deviation resolution)
- Ensure compliance with GMP, FDA, and regulatory requirements
- Provide subject matter expertise and training to operations staff
- Drive readiness for manufacturing operations and sustainable long-term performance
QUALIFICATIONS & REQUIREMENTS:
Education:
- Bachelor’s degree in Engineering, Life Sciences, or related technical field 5+ years of experience in pharmaceutical/biotech or
medical device manufacturing environments
Technical Experience:
- Demonstrated hands-on expertise with terminal sterilization technologies (e.g., steam, EO, dry heat, or other validated
methods)
- Experience designing and implementing sterilization programs or systems at a site or program level
- Experience supporting new facility start-ups or program build-outs
Knowledge, Skills, and Abilities:
- Working knowledge of CQV, validation, and GMP compliance standards Strong documentation, technical writing, and
cross-functional collaboration skills
- Background in process engineering or validation leadership Familiarity with regulatory inspections and audit readiness
- Ability to influence stakeholders and lead multi-disciplinary teams
ESSENTIAL FUNCTIONS:
Physical Demands:
The physical demands described here are representative of the requirements that must be met by an employee to successfully perform
the essential functions of this job. Reasonable accommodations may be made to enable individuals with disabilities to perform the
essential functions.
While performing the duties of this job, the employee is regularly required to use a computer keyboard and mouse; reach with hands
and arms; talk and listen. The employee is frequently required to walk and sit, as well as to lift and carry objects such as books
and files weighing up to 25 pounds. The employee is occasionally required to stand, stoop, or kneel. Specific vision abilities
required by this position include close vision and the ability to adjust focus.
Work Environment:
The work environment characteristics described here are representative of those an employee encounters while performing the
essential functions of this job, including moderate noise level, an indoor temperate environment, and light levels that are bright
and conducive to minimal eye strain, typical for an office environment.
TOTAL REWARDS PROGRAM:
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.
Currently, Syner-G is unable to sponsor or take over sponsorship of an employment Visa at this time.
LEGAL STATEMENT:
Syner-G is proud to be an Equal Employment Opportunity and Affirmative Action employer. All employment decisions, including the
recruiting, hiring, placement, training availability, promotion, compensation, evaluation, disciplinary actions, and termination
of employment (if necessary) are made without regard to the employee’s race, color, creed, religion, sex, pregnancy or childbirth,
personal appearance, family responsibilities, sexual orientation or preference, gender identity, political affiliation, source of
income, place of residence, national or ethnic origin, ancestry, age, marital status, military veteran status, unfavorable
discharge from military service, physical or mental disability, or on any other basis prohibited by applicable law. Syner-G is an
E-Verify employer.
Role
Process Engineer
Category
Other
Location
Published
July 29
Deadline
August 29
Source