My name is Chandrasekhar and I am a Staffing Specialist at Intellectt Inc.
In the past year, we've worked with several medical device clients and helped many candidates to get their careers started.
Hence, I am reaching out to you regarding an exciting job opportunity with one of our clients
Role: Technical Writer
Location: Scarborough, ME - 55345
Duration: 6 Months on W2(Possible Extension)
Shift Timings: 8 AM to 5 PM
Job Description
- Directly participate in a Quality Systems Remediation Program, with the primary responsibility being the creation of high-quality written content.
- Daily Interaction with technical documentation, with documentation tasks to be performed with quantitated high-throughput and attention to detail
- Required to proofread, prepare, create, review, edit, and update Quality and Technical Documents including, but not limited to: SOPs, work/testing instructions, Validation Documentation (IQ / OQ / PQ), Technical Reports, & Record Assessment Reports.
- Understands and is aware of the quality consequences which may occur from the improper performance of their specific job; has awareness of device defects that may occur in their area of responsibility, including product design, verification and validation, manufacturing and testing activities.
- Responsible for exhibiting professional behavior with both internal/external business associates that reflects positively on the company and is consistent with the company's policies and practices; build productive internal/external working relationships.
- Learn complex concepts and communicate the information in a way that is engaging and understood by users.
- Manage and update revision to technical literature.
- Maintain a comprehensive library of technical terminology and documentation.
- Carries out duties in compliance with established business policies.
- Adapt rapidly to a changing industry and be able to adjust responsibilities, time and objectives accordingly.
- Seeking candidates with 3-5 years' experience with technical writing skills and quality documentation in the Medical Device industry - Experience with quality documentations such as non-conformance and risk assessments, CAPA and related documentations.
- Other Skills - Good interpersonal and collaborative skills, ability to multi-task and be organized, exhibit a sense of urgency, and deliver in a timely manner.
If you are looking for any new opportunities feel free to reach me at
Chandrasekhar@intellectt.com
For quick response reach me out at +1732-201-4767