Forge Biologics Inc.
Technical Writer I
Forge Biologics Inc., Columbus, Ohio, United States, 43224
About Forge
Apply promptly! A high volume of applicants is expected for the role as detailed below, do not wait to send your CV.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 currently seeking a
Technical Writer I
to join the Forge Biologics team. This is an exciting opportunity to drive the startup efforts by authoring, reviewing and processing documents needed for our Columbus, Ohio operations. The candidate will collaborate with site Subject Matter Experts (SMEs) in order to transcribe process, procedure and work instructions into usable documents that will support our Quality Management System and adhere to cGMP principles.
The Technical Writer I is responsible for authoring documents in support of all current departments at the Columbus facility. These areas include Safety, Quality, Training, Development, Operations, and Facilities/Engineering efforts. The Technical Writer I will also support new documents that may be deemed necessary as business requires.
What You'll Do
Prepare and update standard operating procedures (SOPs), batch records, protocols, reports, and other technical documents.
Collaborate with scientists, engineers, and other subject matter experts to gather information and translate complex technical data into clear, concise documentation.
Edit, standardize, or suggest changes to material prepared by other writers or Forge personnel to verify accuracy, consistency, grammar, and format.
Observe production, developmental, and experimental activities to determine operating procedure and detail.
Manage document versions and revisions, ensuring that the most current and accurate documents are accessible to all relevant stakeholders.
Study drawings, specifications, mockups, and product samples to integrate and delineate technology, operating procedure, and production sequence and detail.
Review manufacturer's manuals and trade catalogs, drawings and other data relative to operation, maintenance, and service of equipment.
Confer with customer representatives, vendors, facility executives, or publishers to establish technical specifications and to determine subject material to be developed.
What You'll Bring
Bachelor’s Degree or equivalent work experience.
Demonstrated experience with Standard Operating Procedures, Protocols, and Reports.
Previous experience in technical writing, preferably in the pharmaceutical, biotechnology, or related industry, is an advantage but not required.
Intermediate computer software skills including Microsoft Office, Excel and PowerPoint for creation and maintenance of documents, filing, organization, planning skills, managing multiple projects, and time management.
Experience with Veeva Vault, BMRam or equivalent software preferred, Adobe Acrobat PDF/DC experience is strongly desired.
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.
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.
We’ve Got You Covered
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.
Flexible PTO (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.
Wellness benefits (financial planning services, mental health counseling, employer paid disability).
Professional & Personal development resources - LinkedIn Learning, a dedicated training staff in-house, mentoring opportunities & access to leadership development coaches.
#J-18808-Ljbffr
Apply promptly! A high volume of applicants is expected for the role as detailed below, do not wait to send your CV.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 currently seeking a
Technical Writer I
to join the Forge Biologics team. This is an exciting opportunity to drive the startup efforts by authoring, reviewing and processing documents needed for our Columbus, Ohio operations. The candidate will collaborate with site Subject Matter Experts (SMEs) in order to transcribe process, procedure and work instructions into usable documents that will support our Quality Management System and adhere to cGMP principles.
The Technical Writer I is responsible for authoring documents in support of all current departments at the Columbus facility. These areas include Safety, Quality, Training, Development, Operations, and Facilities/Engineering efforts. The Technical Writer I will also support new documents that may be deemed necessary as business requires.
What You'll Do
Prepare and update standard operating procedures (SOPs), batch records, protocols, reports, and other technical documents.
Collaborate with scientists, engineers, and other subject matter experts to gather information and translate complex technical data into clear, concise documentation.
Edit, standardize, or suggest changes to material prepared by other writers or Forge personnel to verify accuracy, consistency, grammar, and format.
Observe production, developmental, and experimental activities to determine operating procedure and detail.
Manage document versions and revisions, ensuring that the most current and accurate documents are accessible to all relevant stakeholders.
Study drawings, specifications, mockups, and product samples to integrate and delineate technology, operating procedure, and production sequence and detail.
Review manufacturer's manuals and trade catalogs, drawings and other data relative to operation, maintenance, and service of equipment.
Confer with customer representatives, vendors, facility executives, or publishers to establish technical specifications and to determine subject material to be developed.
What You'll Bring
Bachelor’s Degree or equivalent work experience.
Demonstrated experience with Standard Operating Procedures, Protocols, and Reports.
Previous experience in technical writing, preferably in the pharmaceutical, biotechnology, or related industry, is an advantage but not required.
Intermediate computer software skills including Microsoft Office, Excel and PowerPoint for creation and maintenance of documents, filing, organization, planning skills, managing multiple projects, and time management.
Experience with Veeva Vault, BMRam or equivalent software preferred, Adobe Acrobat PDF/DC experience is strongly desired.
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.
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.
We’ve Got You Covered
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.
Flexible PTO (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.
Wellness benefits (financial planning services, mental health counseling, employer paid disability).
Professional & Personal development resources - LinkedIn Learning, a dedicated training staff in-house, mentoring opportunities & access to leadership development coaches.
#J-18808-Ljbffr