RESPONSIBILITIES:

Kforce has a client in search of a Technical Writer in New York, New York (NY). This is a 6-month contract to permanent opportunity. The engagement will take place at our NYC location. Consultant during this engagement is expected to travel 10% within the 5 boroughs of NYC.

Summary:
The Technical Writer will be responsible for collecting, organizing, writing, and maintaining technical documentation about the ongoing project(s). The candidate will be responsible for creating presentation slides for work related activities.

Principal Duties and Responsibilities:

• Creating technical documentation and presentations
• Organizing material and complete writing assignment according to set standards regarding order, clarity, conciseness, style, and with accurate terminology
• Conferring with business users, programmers or team members, project leads and managers to establish technical specifications and to determine subject material to be developed for documentation
• Editing, standardizing, or making required changes to the material prepared by other writers or project personnel making sure that the verbiage is correct, the document sections are logically arranged and the content flow is in correct sequence
• Updating published materials and revising them for changes in scope, format, content, storage, and printing
• Maintaining records and files of work and their revisions
• Selecting appropriate photographs, drawings, sketches, diagrams, forms, and charts to use in the documents, published materials, and presentations
• Creating user documentation and manuals for a variety of material, such as How-to Guides and Instruction Manuals
• Adjust copy as necessary and proofread for grammar and spelling, create table of contents, and cite sources
• Submit copies to managers for feedback

REQUIREMENTS:

• Person with a technical editorial background with Bachelor or Master”s degree with English literature, Creative Fine arts, or English major or Journalism
• Prior experience in creating user manuals or technical documentation
• Prior Advertising Industry, journalism knowledge, and experience will be a plus
• Expert knowledge of computer word processor, drawing, flowcharting and presentation software tools and techniques
• Must have excellent grammar, good comprehension, good technical writing skills, and making presentation slides
• Able to listen, read, and understand information and ideas presented in writing, discussions and meetings
• Able to communicate information and ideas clearly, in speech and writing
• Able to write clearly and concisely
• A creative thinker for developing, designing new documents, ideas and presentation
• Able to provide samples of their work

Kforce is an Equal Opportunity/Affirmative Action Employer. All qualified applicants will receive consideration for employment without regard to race, color, religion, sex, pregnancy, sexual orientation, gender identity, national origin, age, protected veteran status, or disability status.

Chat with me now! – https://flashrecruit.com/jobs/298781

Manufacturing Support – Technical Writer

Job Summary

This role is an exciting opportunity to be a critical part of a high growth organization that is radically changing the biotech industry. Currently, the client is building a state-of-the-art, LEED certified, cGMP manufacturing facility in Norwood, MA. This 200k sq. foot campus is critical as we continue to move more of our therapies into the clinic and require in-house manufacturing. The client is seeking a cGMP Manufacturing Support team member focusing on technical writing for our new site in Norwood, MA.

The individual in this role will be part of a cohesive team responsible for producing high quality mRNA-based medicines for evaluation in human clinical trials. The Manufacturing Support Technical Writing team member uses knowledge of cGMP regulations and biopharmaceutical production processes to create and revise standard operating procedures, batch records, specifications, forms and other critical documentation. They will work directly with subject matter experts to ensure content accuracy, improve efficiency and documentation practices.

Job Responsibilities

Heavy documentation, revising and creating SOPs, writing and formatting standard operating procedures and batch records, good comms, word skills, some GMP background and process development – this is budgeted to September, but there is always a chance it can be extended. How documents fit into vision of overall scheme, might be quality control or assurance documents, communicate with groups on their needs, meeting deadlines is critical, ask the right questions when you don”t understand

• Practices and promotes safe work habits and adheres to safety procedures and guidelines
• Conducts document revisions and/or document management
• Utilizes manufacturing process knowledge and documentation skills to identify areas of improvement or gaps within documentation and resolve issues and drive continuous improvement
• Participates in cross functional teams to drive completion of document revisions or creation with a focus on prioritization and timelines for completion
• Participates in cross-functional continuous improvement teams with Engineering, Validation, Quality Assurance, Quality Control, Facilities, and Manufacturing Science and Technology
• Works independently with minimal supervision and direction
• Performs work that consistently requires independent decision making and the exercise of independent judgment and discretion
• Creates and presents trending and metrics reports

Education & Qualifications

• Years of experience range from 2-6 years, but someone more senior than that we can work with.
• Bachelor”s degree in Engineering or Life Sciences is preferred
• High school diploma/GED or Biotech Certification with 2-4 years of experience, or Bachelor”s Degree with 1-2 years of experience in biopharmaceutical operations
• Understanding of biologics drug substance operations or a similar complex specialized environment
• An understanding of regulatory requirements and their applications in a cGMP environment
• Experience with electronic documentation systems for controlled documents in a cGMP environment
• Excellent written and oral English language skills
• Strong skills in the use of Microsoft Word including formatting Demonstrated ability to lead cross functional teams and deliver results with minimal supervision
• Ability to manage multiple competing priorities in a fast-paced environment
• Understanding of lean manufacturing methodologies and operational excellence

Benefits

• Medical, Dental, and Vision Insurance
• 401K Plan with Company Match
• Life and AD&D Insurance

Chat with me now! – https://flashrecruit.com/jobs/298781