Validation Engineer
Company: Syner-G
Location: San Diego
Posted on: February 16, 2026
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Job Description:
Job Description 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. 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 to assist
with the development and execution of validation protocols for
various types of processes. The Validation Engineer will be
responsible for driving overall quality performance and compliance
throughout the organization by defining, implementing, and
maintaining the validation program. We are actively seeking
qualified candidates to join our talent pipeline for future client
engagements. WORK LOCATION: Travel to client sites may be required
up to 100%, based on project demands and client expectations. KEY
RESPONSIBILITIES: (This list is not exhaustive and may be
supplemented and changed as necessary.) Generate and execute life
cycle documentation (FAT, SAT, IOQ, PQ) for cleaning, shipping,
facilities, utilities, systems, equipment, and processes for
(re)qualification/(re)verification. Support validation activities
for Basecamp and client Tech Transfer projects, including
generation, execution, review, and closure of validation life cycle
documents (RA, VP, IQ, OQ, PQ, TM, VR). Write, review, and revise a
variety of Installation, Operation, and Performance
qualification/verification related documents, including any or all
of the following: SOPs, validation/verification master plans,
guidelines and execution plans, automation, engineering design,
commissioning, qualification or other technical documents, user
requirement specifications (URS), functional requirement
specifications (FRS), detailed design specifications, factory
acceptance test documents (FAT), verification protocols, and/or
commissioning test procedures. Write reports to summarize
validation/verification/commissioning and/or
revalidation/verification/commissioning activities. Write
procedures, investigations, protocols, reports, change controls,
etc., to support the Maintenance and Engineering departments.
Perform P&ID Walkdowns. Perform Thermal mapping of
temperature-controlled chambers, warehouses, and SIP processes.
Support the resolution of regulatory observations or manufacturing
site issues. Execute periodic reviews and requalification for
temperature chambers. QUALIFICATIONS AND REQUIREMENTS: To perform
this job successfully, an individual must be able to perform each
essential duty satisfactorily. The requirements listed below are
representative of the education, experience, skills, knowledge, and
abilities required. Reasonable accommodations may be made to enable
individuals with disabilities to perform the essential duties.
Education : Bachelor's degree in a related life science field.
Technical Experience : 4-7 years of experience within the biotech,
pharmaceutical, or medical device industry. Knowledge and
experience working with FDA cGMP, FMEA, and Risk Analysis required.
Validation expertise in Equipment, CSV, Method, and Process.
Protocol generation experience of automated production systems,
with a concentration on computerized equipment and systems
validation. Report writing experience for IQ, OQ, PQ, and CSV.
Knowledge, Skills, and Abilities : Strong verbal and written
communication skills and the ability to discuss technical topics
with non-technical people is strongly desired. 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.
COMPENSATION: The expected salary range for this position is
$90,000 to $120,000. Actual pay will be determined based on
experience, qualifications, geographic location, and other
job-related factors permitted by law. Applicants must have current
work authorization when accepting a position at Syner-G. 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
employers. 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.
Keywords: Syner-G, Oceanside , Validation Engineer, Engineering , San Diego, California