What You Will Do: Our fast-growing medical device company is hiring writers with experience writing technical documents in the field of science and engineering, and we are currently seeking a professional Technical Writer to join this expanding team. The successful applicant will be responsible for creating technical documents and manuals, explain complex information in a clear and concise manner and working with engineering teammates to ensure documentation accuracy. If you have previous experience as a Technical Writer, we encourage you to submit an application.
What You Will Learn: We attract and hire the best talent on the planet! You will be working with a great team of dedicated experts in the Medical Device Industry. You will learn from our Engineers, Clinicians and Manufacturing about our state of the art products.
What You Will Become: A highly influential teammate who can greatly impact the way we support and deliver our material handling and production process.
What Success Looks Like:
Ideal candidate should be familiar with working in a GMP environment as it relates to medical device manufacturing and with writing, proofreading, submitting, and routing technical documents through the approval process.
Create and revise various types of technical documents including validation protocols, work instructions, purchase specifications, CAD drawings, engineering reports, risk assessments, statistical analysis skills, and other project documents and specifications.
The ideal candidate has experience establishing productive working relationships within a cross-functional team, including employees from various inter-facility departments (receiving inspection, manufacturing engineering, R&D, quality, purchasing, materials, etc.) and can work productively without supervision.
Work with engineers as needed to prepare/complete documents, specifications and reports; may support completion of documents/tasks for pending projects
Work with engineers to update dimensional and mechanical features as needed for protocols, reports, specifications, work instructions, etc.
Communicate and negotiate document content and approval with internal employees and external suppliers as needed
Track document review and approval routings; accurately track status of multiple documents
Provide support to various engineering-based projects within an office environment; may be required to complete tasks in production areas. Apply technical writing skills in the form of protocols, test procedures, summary reports, flow charts, specifications and other documents as required.
Create and distribute meeting minutes to document issues, resolutions and action items; follow-up on action items with responsible person(s).
Ability to analyze documents to maintain continuity of style of content
Bachelor’s degree (Preferred)
Government Regulated Environment experience such as FDA or ISO (Preferred)
In absence of medical device industry experience, familiarity with working in another strictly regulated manufacturing industry may be adequate.
Cleanroom Environment Experience (Preferred)
Familiarity with Microsoft Projects, CAD software is beneficial but not required.
Excellent written and verbal communication skills
Proficiency in MS Office
Agile Software or other Documentation Systems experience (preferred)
Strong attention to detail
Skilled at prioritization and multi-tasking
If you have the above qualification and are available to look into this opportunity please send your updated resume along with your contact# and I will call you back to discuss further.
APN Software Services, Inc .
39899 Balentine Drive, Suite 385, Newark, CA 94560 .
Direct: 510.623.5049 | Fax: 510.623.5055 | Email: email@example.com