Technical Writer - Pioneer Data Systems
Sanford, NC 27330
About the Job
Position Details:
Our client, a world-leading Pharmaceutical Company in Sanford, NC is currently looking for a Technical Writer I to join their expanding team.
Job Title: Technical Writer I / Pharma Manufacturing
Duration: 18 months contract, extendable up to 36 months
Location: Sanford, NC
Note:
The client has the right-to-hire you as a permanent employee at any time during or after the end of the contract.
You may participate in the company group medical insurance plan
Job Description:
Technical Writer
Summary:
The Technical Writer will assist with document management system administration at the Sanford, NC site. The role manages document workflows within the Pharmaceutical global electronic document management system and provides administrative approval for document promotions.
In addition, this individual provides guidance to document authors on document workflows and provides input on document standards and requirements.
Responsibilities:
Technical Writing role revises/reformats Standard Operating Procedures (SOPs), training materials, and other related documents in accordance with current approved site templates and subject matter expert requests.
Manages documents through various workflows, ensures document properties are appropriately set, and provides administrative approval for document promotion.
Follows the necessary change management processes to maintain compliance during creation of new and revision of existing documents. Review the impact of proposed changes with regards to other support documents.
Assures new and revised site documentation/procedures are:
Current and consistent with related/similar documents.
Meet internal control policies and regulations.
Qualifications:
Minimum High School Diploma with a minimum of 3+ years experience documentation-related or supporting function is required, preferably in a Biopharmaceutical or other regulated environment OR Bachelor's degree with 1 - 2+ years' of experience in documentation-related or supporting function is required, preferably in a Biopharmaceutical or other regulated environment.
Able to quickly learn and navigate electronic systems to facilitate routine operation and maintenance of the site documentation system and related processes.
Able to write clearly and concisely with excellent grammar, good writing skills and communication.
Skilled in word processing and document formatting; experienced in Microsoft Office applications (Word, Excel, PowerPoint, Visio).
Able to effectively proofread documents prepared by self and others for content and others to ensure content and formatting accuracy.
Demonstrates an ability to adapt to shifting priorities, change, stress and to find appropriate balance between needs of the organization, others and self. Incorporates insights of other people into ongoing work.
Understanding of cGMP and Safety regulations.
Strong organizational and communication skills.
Team based collaborative problem solving.
This role will be onsite in Sanford, NC
Our client, a world-leading Pharmaceutical Company in Sanford, NC is currently looking for a Technical Writer I to join their expanding team.
Job Title: Technical Writer I / Pharma Manufacturing
Duration: 18 months contract, extendable up to 36 months
Location: Sanford, NC
Note:
The client has the right-to-hire you as a permanent employee at any time during or after the end of the contract.
You may participate in the company group medical insurance plan
Job Description:
Technical Writer
Summary:
The Technical Writer will assist with document management system administration at the Sanford, NC site. The role manages document workflows within the Pharmaceutical global electronic document management system and provides administrative approval for document promotions.
In addition, this individual provides guidance to document authors on document workflows and provides input on document standards and requirements.
Responsibilities:
Technical Writing role revises/reformats Standard Operating Procedures (SOPs), training materials, and other related documents in accordance with current approved site templates and subject matter expert requests.
Manages documents through various workflows, ensures document properties are appropriately set, and provides administrative approval for document promotion.
Follows the necessary change management processes to maintain compliance during creation of new and revision of existing documents. Review the impact of proposed changes with regards to other support documents.
Assures new and revised site documentation/procedures are:
Current and consistent with related/similar documents.
Meet internal control policies and regulations.
Qualifications:
Minimum High School Diploma with a minimum of 3+ years experience documentation-related or supporting function is required, preferably in a Biopharmaceutical or other regulated environment OR Bachelor's degree with 1 - 2+ years' of experience in documentation-related or supporting function is required, preferably in a Biopharmaceutical or other regulated environment.
Able to quickly learn and navigate electronic systems to facilitate routine operation and maintenance of the site documentation system and related processes.
Able to write clearly and concisely with excellent grammar, good writing skills and communication.
Skilled in word processing and document formatting; experienced in Microsoft Office applications (Word, Excel, PowerPoint, Visio).
Able to effectively proofread documents prepared by self and others for content and others to ensure content and formatting accuracy.
Demonstrates an ability to adapt to shifting priorities, change, stress and to find appropriate balance between needs of the organization, others and self. Incorporates insights of other people into ongoing work.
Understanding of cGMP and Safety regulations.
Strong organizational and communication skills.
Team based collaborative problem solving.
This role will be onsite in Sanford, NC
Source : Pioneer Data Systems