Sr. Manufacturing Associate/Manufacturing Associate
Company: Landmark Bio
Location: Watertown
Posted on: January 15, 2026
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Job Description:
Job Description Job Description Landmark Bio is dedicated to
translating cutting-edge research into life-changing therapies.
Headquartered in Watertown, Massachusetts, the company was founded
by leading academic institutions, research hospitals, and industry
partners to accelerate the development, manufacturing, and
commercialization of advanced therapies. Driven by the compelling
science and transformative potential of genetic medicine, Landmark
Bio offers deep drug development expertise and integrated
end-to-end solutions to support its partners. The company also
serves as a collaborative platform to advance next-generation
manufacturing technologies for novel modalities. Following its
acquisition by Artis BioSolutions in 2025, Landmark Bio continues
to operate as a distinct entity. Learn more at www.landmarkbio.com.
We are seeking a highly motivated and team-oriented professional
with entrepreneurial spirit to join our company! This is an
exciting opportunity for a well-qualified candidate to join a
rapidly growing company focused on turning today’s cutting-edge
research into tomorrow’s breakthrough therapies. We are seeking a
highly motivated, team-oriented, and entrepreneurial-minded
individual for the position of Sr. Manufacturing
Associate/Manufacturing Associate in Landmark Bio’s Manufacturing
Operations group. Manufacturing Operations is responsible for
executing cell therapy, vector manufacturing, fill finish and
production support operations following current Good Manufacturing
Practices (cGMP) in cleanroom environments to produce materials for
use in early-stage clinical trials. In addition to hands-on
operations, Sr. Manufacturing Associates work with colleagues in
Process Development, Facilities & Engineering and Quality Assurance
to support batch documentation, deviation investigations and
corrective actions, and new technology introduction. This is an
exciting opportunity for a well-qualified candidate to join a
rapidly growing company focused on turning today’s cutting-edge
research into tomorrow’s breakthrough therapies. Together with our
partners and collaborators, we are effecting broader changes in the
healthcare industry and making a positive impact on people’s lives
and our society. Scope of Responsibilities · Adheres to all safety
protocols and maintains safe work habits in compliance with
organizational and regulatory standards. · Performs aseptic
operations for cell culture, viral transfection, cell harvesting,
and purification processes, ensuring contamination control and
compliance with GMP. · Collaborates with cross-functional teams,
including Quality Assurance, Quality Control, and Process
Development, to support continuous improvement initiatives and
maintain manufacturing readiness. · Executes manufacturing
operations for cell and gene therapy products, with a focus on
viral vector production and cell processing in a cGMP-compliant
environment. · Completes and documents all required training before
performing cGMP manufacturing activities. · Handles equipment
assembly, operation, disassembly, and cleaning, ensuring readiness
and cleanliness standards are met. · Follows and accurately
documents standard operating procedures (SOPs) and batch records,
ensuring thorough and precise data entry. · Supports document
management by assisting with authoring, updating, and revising
batch production records and SOPs. · Assists in implementing new
manufacturing technologies and procedures to enhance operational
efficiency and effectiveness. · Contributes to training efforts by
supporting the onboarding and development of team members. · Serves
as a Subject Matter Expert (SME) for designated equipment,
providing technical support and guidance. · Participates in
technical transfer activities to integrate processes into the cGMP
facility effectively. · Leads or supports investigations as needed
to address process deviations and implement corrective actions. ·
Applies process knowledge to resolve manufacturing issues and
identify areas for continuous improvement. · Engages in
cross-functional teams to drive deviation investigations, conduct
root cause analysis, and support Corrective and Preventative
Actions (CAPAs). Qualifications · Bachelor’s degree with a minimum
of 2 years of experience in a cGMP manufacturing environment, or a
combination of relevant education and experience. · Experience in
cell processing, viral vector production, and single-use platforms
is preferred. · Working knowledge of cGMP and regulatory standards
with familiarity in deviation management, CAPAs, and Change Control
processes. · Ability to perform aseptic gowning and execute
manufacturing tasks while adhering to gowning and personal
protective equipment (PPE) standards. · Proficient in basic
computer skills with a willingness to learn new systems and adapt
to emerging technologies. · Strong organizational and interpersonal
skills, with excellent written and oral English language
communication abilities. Landmark Bio is an Equal Opportunity,
Affirmative Action employer. Minorities, women, veterans, and
individuals with disabilities are encouraged to apply. It is
unlawful in Massachusetts to require or administer a lie detector
test as a condition of employment or continued employment. An
employer who violates this law may be subject to criminal penalties
and civil liability. We may use artificial intelligence (AI) tools
to support parts of the hiring process, such as reviewing
applications, analyzing resumes, or assessing responses. These
tools assist our recruitment team but do not replace human
judgment. Final hiring decisions are ultimately made by humans. If
you would like more information about how your data is processed,
please contact us.
Keywords: Landmark Bio, Boston , Sr. Manufacturing Associate/Manufacturing Associate, Science, Research & Development , Watertown, Massachusetts
