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Technician I, GMP Manufacturing - Fill/Finish

About Forge  

Forge, a member of Ajinomoto Bio-Pharma Services, is a gene therapy development engine, focused on enabling access to life changing gene therapies and helping bring them from idea into reality. We partner with innovators in the gene therapy community: scientists, physicians, biotech/pharma companies, and patient groups. We bring expertise in gene therapy manufacturing and therapeutics development to the table, helping to champion teams that are navigating the long road from the lab bench to the bedside. Our goal is simple but vital to patients living with disease, and we take it seriously. With a patient-first approach, we are forging new models for working together to better accelerate these transformative medicines to reach those who need them the most.   

Forge is based in Columbus, Ohio, in a 200,000 square foot facility known affectionately by team members as, the Hearth. The Hearth, is a custom-designed cGMP facility dedicated to AAV manufacturing and hosts scalable, end-to-end manufacturing services.    

About The Role  

We are seeking a detail-oriented and highly motivated individual to join our Fill/Finish Manufacturing team. As a Technician I, GMP Manufacturing – Fill/Finish you will play a crucial role in the aseptic filling and finishing operations of AAV-based gene therapy products in compliance with current Good Manufacturing Practices (cGMP) regulations. This position presents an exciting opportunity to contribute to the manufacturing of cutting-edge therapies that have the potential to transform the lives of patients.

What You’ll Do  

  • Execute aseptic filling and finishing operations according to Standard Operating Procedures (SOPs) and batch records, ensuring compliance with cGMP guidelines and quality standards.
  • Prepare and operate filling equipment, such as semi-automated and automated fillers, stoppering machines, cappers, and labeling machines, following established procedures, and ensuring proper setup, calibration, and maintenance.
  • Perform line clearances, sanitization, and sterilization of equipment and manufacturing areas to maintain aseptic conditions.
  • Assemble, disassemble, and clean equipment components, ensuring proper sterilization procedures are followed.
  • Monitor critical process parameters, including fill volumes, stopper/cap placement, torque, and label alignment, and promptly report deviations or abnormalities.
  • Conduct in-process testing and quality control checks, such as visual inspections, particle count, and container closure integrity tests, to ensure product quality and compliance.
  • Accurately document manufacturing activities and data in compliance with cGMP regulations and company policies.
  • Collaborate with cross-functional teams, to investigate and resolve deviations, non-conformances, and quality incidents.
  • Support process improvement initiatives to enhance efficiency, productivity, and compliance.
  • Follow safety protocols and environmental health guidelines to maintain a safe workspace.
  • Participate in training programs and stay updated with current industry trends, regulatory requirements, and advancements in gene therapy manufacturing processes.

What You’ll Bring  

  • Associate’s or Bachelor’s degree in a scientific, technical, or related field preferred; or equivalent professional experience.
  • Previous experience working in a regulated manufacturing or laboratory environment.
  • Excellent organizational skills and the ability to multitask in a fast-paced environment while adhering to strict timelines.
  • Strong teamwork and communication skills to collaborate effectively across departments.
  • Commitment to following SOPs, safety protocols, and regulatory guidelines to ensure compliance and product quality.
  • Ability to adapt to changing priorities and work independently as well as part of a team.
  • Strong problem-solving skills and ability to identify and escalate issues as needed.
  • Willingness to work flexible hours, including evenings, weekends, and holidays to support manufacturing production schedules.
  • Ability to stand for extended periods, and work in a cleanroom environment while wearing appropriate gowning and PPE.

 Preferred Skills   

  • Prior experience working in a cGMP manufacturing environment.
  • Experience operating and maintaining filling and finishing equipment
  • Familiarity with aseptic filling equipment and processes, such as semi-automated and automated fillers, stoppering machines, cappers, and labeling machines

Work Environment and Physical Demands  

This position works in both a laboratory environment and typical office environment where the physical work demands will vary depending on the specific tasks and duties required of the job. The employee will be stationary (standing/sitting) for extended periods of time. Employees regularly wear personal protective equipment based on the task being performed. Must be able to work in a confined space, such as a clean room or laboratory environment. Ability to identify small details within the field of vision, distinguish between different colors, and accurately identify objects within a specific area.

This job description is not designed to cover or contain a comprehensive listing of activities, duties or responsibilities that are required of the employee. Duties, responsibilities and activities may change or new ones may be assigned.  

Forge Biologics is an equal opportunity employer dedicated to building an inclusive and diverse workforce. Forge Biologics, provides equal employment opportunities to all employees and applicants for employment and prohibits discrimination and harassment of any type without regard to race, color, religion, age, sex, national origin, disability status, genetics, protected veteran status, sexual orientation, gender identity or expression, or any other characteristic protected by federal, state or local laws. 

Life at Forge  

We are a team of diverse, driven and passionate people working together to trailblaze a new model for how we make medicines to treat patients with genetic diseases. Our team members use their creativity and talent to invent new solutions, meet new demands, and offer the most effective services in the industry. Forge’s core values lay the foundation for H.O.P.E. It provides us a common purpose that we all understand, work towards and live by.  

HARDWORKING - We work hard and smart, making a persistent and determined effort toward success. Working hard, with focus and desire is the key. 

OPEN - We strive to be approachable, actively listen and encourage others to contribute and speak up. We positively offer and receive constructive feedback. 

PURPOSE DRIVEN - We are passionate about working towards and delivering on our mission to manufacture gene therapies. 

ENGAGED - We are fully absorbed by and enthusiastic about our work and take positive action to further Forge’s vision, mission and goals. 

We’ve Got You Covered 

We take the health and happiness of our employees seriously and are consistently evaluating new ways to make our benefits truly UnFORGEttable. 

  • Health, Dental, and Vision insurance that starts on your first day at Forge, with 90% of premiums covered for team members as well as dependents 
  • Competitive PTO plan (plus 14 paid company holidays) 
  • Annual bonus for all full-time employees 
  • 401(K) company match 
  • Fully-stocked kitchen with free food/drinks 
  • 12 weeks of paid parental leave - additional discount programs include childcare support & dependent care 
  • Employee Assistance Program  
  • Onsite gym
  • Wellness benefits (financial planning services, mental health counseling, employer paid disability) 
  • Professional & Personal development resources 
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Average salary estimate

$60000 / YEARLY (est.)
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$50000K
$70000K

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Enable access to life changing gene therapies and help bring them from idea into reality.

53 jobs
MATCH
VIEW MATCH
FUNDING
DEPARTMENTS
SENIORITY LEVEL REQUIREMENT
TEAM SIZE
SALARY RANGE
$50,000/yr - $70,000/yr
EMPLOYMENT TYPE
Full-time, on-site
DATE POSTED
April 25, 2025

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