Technical writer Job at Randstad in Largo

job summary:
Randstad is the #1 HR Solutions Company in the World and we are sourcing for a Technical Writer in the Tampa Bay, FL area. The ideal candidate will support quality control with written documentation management. You will also create new or revise existing content for regulatory documentation and compile data in accordance with industry best practices, cGMP requirements and corporate guidelines. Work collaboratively with team members including Quality Assurance, Document Control, and other subject-matter experts (SMEs) to solidify content. This is a contract position and can start immediately.

location: Largo, Florida
job type: Contract
work hours: 8 to 4
education: Bachelors

responsibilities:
RESPONSIBILITIES:

• Provide inter-departmental support with written documentation, including Material Inspection Records and Product Testing Specifications (Intermediate/Filling).
• Review, edit, standardize, or make changes to material prepared by other writers or facility personnel as instructed by Area SMEs.
• Organize material and complete writing assignments according to set standards regarding order, clarity, conciseness, style, and terminology.
• Work with various department personnel to gain understanding of equipment/procedures/processes and translate into written procedures.
• Understand different user levels and write documents that meet the need of the end user.
• Keep record and provide updates on document deliverables to project owner and ensure that documents are delivered to the customer (either internal or external) in a timely manner.
• Performing other duties as assigned.

qualifications:
REQUIREMENTS:

• The ability to manage multiple projects at a time.
• The ability to communicate well with others through speech and text
• Process complex thoughts and communicate them efficiently to the end user. Must be able to work independently as well as in a team environment.
• Good command of MS Office Suite (Word, Excel, PowerPoint, and Outlook).
• Strong working knowledge of editing, proofreading, spelling, grammar, formatting and punctuation.
• Proficient in computer and software literacy.

PREFERRED ADDITIONAL:

• Experience in cGMP environment.
• Experience in a Quality Laboratory a plus
• Experience in an agile team working in a fast-paced environment.
• Bachelor's degree or experience equivalent to Duties/Responsibilities for a minimum of 2 years.
• Knowledge in interpreting and implementing quality documents/specifications applicable to documentation update.

skills: Editing, Quality control, SOP, Quality Assurance, Data Analysis, Administration, File Management, Biology, Chemistry, GLP (Good Laboratory Practice), Data Validation Plan, Regulatory Briefing Documents, GMP (Good Manufacturing Practice)

Equal Opportunity Employer: Race, Color, Religion, Sex, Sexual Orientation, Gender Identity, National Origin, Age, Genetic Information, Disability, Protected Veteran Status, or any other legally protected group status.

At Randstad, we welcome people of all abilities and want to ensure that our hiring and interview process meets the needs of all applicants. If you require a reasonable accommodation to make your application or interview experience a great one, please contact HRsupport@randstadusa.com.

Pay offered to a successful candidate will be based on several factors including the candidate's education, work experience, work location, specific job duties, certifications, etc. In addition, Randstad offers a comprehensive benefits package, including health, an incentive and recognition program, and 401K contribution (all benefits are based on eligibility).

This posting is open for thirty (30) days.