Technical Writer / Medical writer / Manufacturing Writer

TekWissen ®

East Walpole (MA)

On-site

USD 65,000 - 85,000

Full time

2 days ago
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Job summary

TekWissen LLC is seeking a Manufacturing Technical Writer II to produce, edit, and process compliant Quality System documents for manufacturing, including work instructions, forms, and procedures. You will work with Manufacturing, Quality, Engineering and Technical teams to learn products/processes and write accurate documentation.

The role emphasizes attention to detail, organization, and the ability to manage multiple documents while meeting deadlines.

Qualifications

  • 3–5 years of technical writing experience required.
  • Strong verbal and written communication skills.
  • Demonstrated attention to detail and organization.
  • Ability to work independently and manage multiple documents.
  • Proficiency with Microsoft Word, Excel and PowerPoint.

Responsibilities

  • Produce compliant, high-quality manufacturing documentation.
  • Edit and process manufacturing work instructions and forms.
  • Create flow charts, diagrams, and visual aids.
  • Collaborate with Manufacturing, Quality, Engineering and Technical teams.
  • Support documentation needs for process scale-ups.
  • Gather feedback and improve documents; maintain project timelines.
  • Provide training support for document change processes.

Skills

Technical writing
Attention to detail
Communication skills
Independent work
Microsoft Office
Data presentation
Deadline management
SAP (plus)

Tools

SAP

Job description

TekWissen is a global workforce management provider headquartered in Ann Arbor, Michigan, offering strategic talent solutions tclients worldwide. The opportunity below is with one of our clients, a leading global medical technology company. This organization provides a wide range of diagnostic imaging and laboratory diagnostics, as well as advanced therapies and digital health services. Its solutions span prevention and early detection through diagnosis, treatment, and follow-up care, empowering healthcare providers worldwide.

Position Description:
  • Writes and edits technical documentation for products, processes and/or projects (user manuals, job aids, technical instructions/bulletins etc.).
  • Researches technical and engineering information, including drawings, design and test specifications, product prototypes, and interviews with subject matter experts.
  • Completes all phases of document development cycle, including project scope and requirements, documentation design, etc.
Impacts:
  • Needs professional technological, economical or scientific know how, methods, tools and principles, and applies to differing and variable situations.
  • Needs to solve assigned, non-routine tasks, to contribute to projects or assignments, or to support development of guidelines, methods, tools or business processes.
Key Responsibilities:
  • "Experienced Professional" These positions are expected to contribute to and deliver business processes or detailed technology solutions, in a self-managed and target oriented manner, and thus contribute to team results.
  • Positions focusing on analyzing, developing, testing or implementing processes, technologies and systems in their specific field of expertise, from first principles.
  • Targets are short to medium term (best to be characterized as milestones), and achievements are monitored.
  • They may provide functional advice to and integrate services of operational staff or semi-professional colleagues.
Knowledge:
  • Good knowledge in a technical field or business method including the basic theoretical background.
  • Develops basic business understanding.
  • Contributes to team effort, awareness of expected value add.
  • May improve processes, business methods or technical components.
Job Responsibilities:
  • The primary role of this individual is to produce compliant high-quality documentation.
  • This role encompasses the support and coordination of writing, editing, and/or processing compliant documents and procedures in Manufacturing.
  • The core competencies that are essential to success are attention to detail and organization.
  • Critical thinking, with a solid understanding of quality implications, is necessary in managing document writing efficiently and compliantly.
  • Communication is needed to maintain visibility of the documents and progress of the product/project.
  • This is a role well suited to an ambitious professional, looking for the next step in their career.
  • As a Manufacturing Technical Writer II, this role will be responsible for:
  • Write, edit, and/or process compliant Quality System documents and procedures including manufacturing work instructions, manufacturing forms, guidance procedures, and risk files.
  • Create and/or edit flow charts, diagrams, and other visual aids.
  • Collaborate with Manufacturing, Quality, Engineering, and Technical organizations to learn about specific products or processes to write and/or edit documents and/or procedures.
  • Support documentation needs for manufacturing related projects e.g., process scale ups.
  • Gather and apply feedback to improve documents and/or procedures.
  • Communicate status and meet project timelines and deadlines.
  • Provide training support for the document change process.
Required Education, Skills & Experience:
  • Strong verbal and written communication skills, organization.
  • 3-5 years of technical writing experience.
  • A high level of attention to detail.
  • Strong organizational skills.
  • Ability to work independently to create, track, and report on plans/projects to complete multiple documents and/or projects in a timely manner.
  • Ability to present complex data in clear, concise text.
  • Ability to meet deadlines and work independently.
  • Proficient with Microsoft Office products, including Word, Excel, and PowerPoint.
Preferred Experience:
  • A background in SAP is a plus.

TekWissen® Group is an equal opportunity employer supporting workforce diversity.

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