Technical Writer I (Manufacturing/Quality) 1st Shift

Immediate need for a talented Technical Writer I (Manufacturing/Quality) 1st Shift. This is a 07+months contract opportunity with long-term potential and is located in Swiftwater, PA (Onsite). Please review the job description below and contact me ASAP if you are interested.

Job ID: 25-71122

Pay Range: $30 - $40/hour.  Employee benefits include, but are not limited to, health insurance (medical, dental, vision), 401(k) plan, and paid sick leave (depending on work location).

Key Responsibilities:

• Technical Writer needed to support ERP deployment to Manufacturing and Supply organization.
• 1st Shift: Responsible for designing, developing, and updating required technical documentation.
• Responsible for technical writing/editing for all types of documentation produced within a modern software development environment.
• Utilize knowledge of word processing software, strong writing and analytical skills to document software capabilities and functionality.
• Document programming standards and procedures.
• Track and review change control documentation.
• Assist with the editing of quality documents (SOP's, guidelines, validation master plans, etc.) to ensure compliance with regulatory requirements.
• Must be able to work quickly with a high degree of accuracy.
• Must possess sound interpersonal and information gathering skills, be able to relate well to others at all levels throughout the organization and have the ability to work in a team environment, effectively interacting with others.
• Review current documents- incorporate comments from Manager.
• Navigate through Client EDoc (Documentum) system utilizing current templates.
• Notify manager of workflow status and issues.
• Incorporate comments from team members and provide status to manager on review and approval workflow.
• Follow up with team members on comments

Key Requirements and Technology Experience: 

• Key skills; Document management system/EDoc (Documentum)
• Quality document
• Technical writing/editing
• SOP's
• GMP experience/working in a validated environment
• Manager In-take notes: Fully onsite, M-F 8/9am - 4/5pm, Possibility to extend after December depending on workload.
• Day in the life: Team based: updating docs, work with key users to review and make changes, routing for review in doc management systems, following up on comments, tracking approvals...
• 0-3 years exp, Bach degree preferred.
• Must Haves: 1. Need exp working in doc management system 2. Strong MS Word 3. Strong communication skills 4. GMP experience/working in a validated environment
• Technical writing abilities and good time management.
• Strong root cause analysis skills with experience regarding quality standards.
• Be able to establish working relationships with other support and production areas in order to gather all the necessary information required.
• Must be proficient in EDoc with a working knowledge of templates, workflows and approval process.
• Proficient in MS Word, Excel, Powerpoint and Outlook. Interact well with a diverse group of individuals.
• Self-motivated and willing to be proactive in resolving issues.
• Excellent Verbal and written communication skills.
• Ability to work in a team environment.
• Education: University graduate preferred.
• Secondary Education diploma a requirement..
• Years of Experience: 0 - 3 Years

Our client is a leading pharmaceutical Industry and we are currently interviewing to fill this and other similar contract positions. If you are interested in this position, please apply online for immediate consideration.

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