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Syner-G

Validation Engineer

Plainville, MA, United States

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Job details

Experience: 4–7 years of experience in the biotech, pharmaceutical, or medical device industry.
Posting language: English
Posted: Nov 3, 2026

Original job description

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.

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

POSITION OVERVIEW

We are seeking a Validation Engineer with 4-7 years of experience to support commissioning, qualification, validation (CQV), and computer system validation (CSV) activities across equipment, utilities, facilities, laboratory systems, manufacturing processes, and computerized systems. This role will be responsible for developing, executing, reviewing, and maintaining validation lifecycle documentation, with a strong emphasis on qualification records managed within the Kneat validation platform.

The Validation Engineer will collaborate with cross-functional teams to ensure validation activities are completed in compliance with GMP regulations, data integrity requirements, internal quality standards, and project timelines. This position plays a critical role in supporting operational readiness, technology transfer, change management, and continuous improvement initiatives.

KEY RESPONSIBILITIES

(This list is not exhaustive and may be supplemented or adjusted as needed.)

• Develop, review, execute, and maintain commissioning, qualification, and validation protocols and reports within the Kneat validation system.

• Generate and execute validation lifecycle documentation, including FAT, SAT, IQ, OQ, PQ, and CSV deliverables for equipment, utilities, facilities, laboratory systems, manufacturing processes, and other GMP-regulated assets.

• Author, execute, review, and close validation documents including validation plans, risk assessments, protocols, reports, discrepancy investigations, and summary reports.

• Support qualification and validation activities for analytical laboratory equipment, manufacturing systems, and computerized systems in accordance with applicable regulatory requirements.

• Support technology transfer projects through validation planning, protocol execution, documentation review, and qualification activities.

• Develop and revise validation documentation, including SOPs, Master Validation Plans, execution plans, URS, FRS, design specifications, commissioning protocols, verification protocols, and test procedures.

• Collaborate with Engineering, Manufacturing, Quality Assurance, Quality Control, and project teams to ensure successful execution of validation activities.

• Support change controls, impact assessments, deviation investigations, CAPAs, and validation assessments for GMP systems and processes.

• Perform P&ID walkdowns and system inspections to verify installation and operational readiness.

• Conduct thermal mapping studies and support qualification activities for controlled environments and temperature-controlled systems.

• Support regulatory inspections, audits, and remediation activities related to validation and qualification programs.

• Perform periodic reviews, requalification activities, and lifecycle management of validated systems and equipment.

• Ensure all validation documentation complies with current GMP requirements, data integrity expectations, Good Documentation Practices (GDP), and company procedures.

• Independently manage assigned validation projects while effectively communicating status, risks, resource needs, and project milestones.

QUALIFICATIONS AND REQUIREMENTS

To perform this job successfully, an individual must be able to perform each essential duty satisfactorily. Reasonable accommodations may be made to enable individuals with disabilities to perform the essential functions.

Education

Bachelor’s degree in a life science, engineering, or related technical field.

Technical Experience

4–7 years of experience in the biotech, pharmaceutical, or medical device industry.
Strong knowledge of FDA cGMP requirements, FMEA, and risk‑based validation principles.
Hands‑on validation experience in equipment, computerized systems (CSV), analytical methods, and process validation.
Experience generating protocols for automated production systems, with emphasis on computerized equipment and systems validation.
Demonstrated experience writing IQ, OQ, PQ, and CSV reports.

Knowledge, Skills, and Abilities

Strong verbal and written communication skills, with the ability to explain technical concepts to non‑technical stakeholders.
Detail‑oriented with strong organizational and documentation skills.
Ability to work independently and collaboratively in a fast‑paced, regulated environment.
Strong problem‑solving skills and the ability to support investigations and root‑cause analysis.

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.

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More about this job

Skills

Manufacturing processes
Documentation
Regulatory compliance
Good manufacturing practices
Change management
Process improvement
SAP IQ
Laboratory equipment
Test procedures
Quality assurance
Quality control
Inspection
Communication skills
Work independently
Problem solving
Root cause analysis
Use a computer
Carry objects

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