Medical Writer/Technical Writer

Artech is the 10th Largest IT Staffing Company in the US, according to Staffing Industry Analysts' 2012 annual report. Artech provides technical expertise to fill gaps in clients' immediate skill-sets availability, deliver emerging technology skill-sets, refresh existing skill base, allow for flexibility in project planning and execution phases, and provide budgeting/financial flexibility by offering contingent labor as a variable cost.

Summarize the primary purpose & key accountabilities of the position, including scope of responsibility in 5-7 concise sentences. (i.e. Global vs. Country/Region) It may be helpful to complete this section after you have finished the other sections of the document.

Incumbent will assist in the creation, review and revision of documents (SOPs, forms, jobs aids, training material, etc.) and other manufacturing department documents. Incumbent will work with co-workers and supervisors to understand the objective of each document to ensure that all documents contain the required content. Incumbent will interpret information and organize it properly for accuracy, readability and format, while ensuring the proper grammar and spelling is used in all documents. Perform all duties in a manner consistent with site and corporate cGMP, safety, environmental and human resources policies and procedures.

POSITION RESPONSIBILITIES 

• In order of importance, list the primary responsibilities critical to the performance of the position. It is recommended not to list actual tasks but focus on essential responsibilities that highlight accountability and level of judgment required.

• Edit and format incoming requests for new or revised documents (SOPs, forms, jobs aids, training material, etc.) and assist in tracking each revision through the approval workflow.

• Provide assistance with development of new and revised documents including suggestions for suitable terminology, content, and format while ensuring that site policies comply with Corporate guidelines.

• Participate in the bi-annual review of Standard Operating Procedures, forms and other related documents. Complete commitments as assigned to facilitate Corrective Actions/Preventative Actions.

• Participate in the bi-annual review of Standard Operating Procedures, forms and other related documents. Complete commitments as assigned to facilitate Corrective Actions/Preventative Actions.

• Assist in maintaining control of documentation to include accurate document history and change revision documentation.

EDUCATION AND EXPERIENCE 

• Indicate the formal education, certification or license required and/or preferred. Include the minimum number of years of relevant experience required for the position (where legally permissible).

• Bachelor s degree in Science, Communications, or English, with at least 2 years related experience in technical writing, preferably in a pharmaceutical or related environment

• AS in Communications or related field with minimum of 5 years related experience in technical writing, preferably in a Biopharmaceutical or other regulated environment.

TECHNICAL SKILLS REQUIREMENTS 

• Indicate the technical skills required and/or preferred, as applicable.

• Able to edit documents quickly and efficiently to incorporate required revisions

• Develops and applies standardized document formats where applicable.

• Able to learn and navigate document control and e-systems to facilitate document routing and approval

• Able to effectively proofread documents prepared by self and others for content and others to ensure accuracy.

• Able to write clearly and concisely with strong English background with excellent grammar, good writing skills and knowledge of sentence structure

• Effective active listening skills. Able to translate verbal guidance into precise operating instructions

• Adheres to and applies standard document formats while maintaining technical content of new and revised documents

• 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.

• Able to learn and understand pharmaceutical processes in order to design related SOPs.

• Understanding of cGMP and Safety regulations

• Strong organizational and communication skills

• Team based collaborative problem solving

• Strong understanding of cGMPs

Best Regards,

Anuj Mehta

973-967-3402