Forge Biologics is hiring: Technician II, GMP Manufacturing - Upstream in Columb

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 Team The GMP Manufacturing department is responsible for the manufacturing of AAV Gene Therapy products in accordance with the highest standards of Good Manufacturing Practices (GMPs). This department ensures that the products produced are of the highest quality and meet all applicable regulatory requirements. This team works together to ensure the production of safe and effective Gene Therapy products.About The RoleWe are seeking an experienced and detail-oriented individual to join our Upstream Manufacturing team. As a Technician II, GMP Manufacturing - Upstream you will play a critical role in the production and cultivation of AAV-based gene therapy products in compliance with current Good Manufacturing Practices (cGMP) regulations. This position offers an exciting opportunity to utilize your expertise in upstream bioprocessing and contribute to the manufacturing of cutting-edge therapies that have the potential to transform the lives of patients.What You'll DoExecute and oversee upstream manufacturing operations, including cell culture expansion, transfection, and harvest steps, according to Standard Operating Procedures (SOPs) and batch records.Independently prepare and operate bioreactors, centrifuges; filtration systems, and other equipment required for upstream processing, ensuring proper calibration, maintenance, and troubleshooting when needed.Perform complex media and buffer preparation, as well as the aseptic transfer of materials, adhering to cGMP guidelines and maintaining a clean and organized work area.Monitor critical process parameters during manufacturing operations, analyze data, and proactively identify and report deviations or abnormalities to the supervisor.Conduct sampling and in-process testing, such as cell counts, viability, and metabolite analysis, and other analytical techniques, to ensure optimal culture conditions and product quality.Lead and document all manufacturing activities, data, and results accurately and in compliance with cGMP regulations and company policies.Collaborate with cross-functional teams, including Quality Assurance (QA) and Quality Control (QC), to investigate and resolve deviations, non-conformances, and quality incidents related to upstream manufacturing processes.Contribute to process improvement initiatives, including evaluating new technologies, equipment, and methods to enhance manufacturing efficiency, productivity, and compliance.Mentor and train GMP Technicians I, providing guidance on process execution, troubleshooting, and adherence to cGMP guidelines.Ensure safety procedures and environmental health and safety guidelines are followed, maintaining a safe working environment.Stay updated with current industry trends, regulatory requirements, and advancements in gene therapy manufacturing processes and share knowledge with team.Additional responsibilities not listed may be assigned as needed by management.What You'll Bring Associate's or Bachelor's Degree (B.A. or B.S.) in Biology, Biochemistry, Biomedical Engineering or related life science field (or equivalent professional experience).3+ years of experience working in a GxP or regulated environment.Strong knowledge and hands-on experience with cell culture techniques, bioreactors (e.g., single-use bioreactors), centrifuges, filtration systems, and other upstream processing equipment.Proficiency in media and buffer preparation, aseptic techniques, and analytical methods commonly used in upstream manufacturing.Excellent attention to detail and ability to accurately document and record experimental data and manufacturing activities.Strong organizational skills and the ability to manage multiple tasks and prioritize effectively in a fast-paced environment.Excellent interpersonal and communication skills, both written and verbal, to effectively collaborate with team members and stakeholders.Commitment to following SOPs, safety protocols, and regulatory guidelines to ensure compliance and product quality.Demonstrated leadership abilities, including the ability to mentor and train junior team members.Flexibility to work in shifts, including weekends and holidays, as required by manufacturing schedules.Preferred SkillsPrior experience working in a cGMP manufacturing environment.Upstream bioprocessing or biologics manufacturing experience.Basic understanding of viral vector-based gene therapy processes, principles, and quality requirements.Work Environment & Physical DemandsThis 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 CoveredWe 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 dependentsFlexible PTO (plus 14 paid company holidays)Annual bonus for all full-time employees401(K) company matchFully-stocked kitchen with free food/drinks12 weeks of paid parental leave - additional discount programs include childcare support & dependent careEmployee Assistance ProgramWellness benefits (financial planning services, mental health counseling, employer paid disability)Professional & Personal development resources - LinkedIn Learning, a dedicate training staff in-house, mentoring opportunities & access to leadership development coaches