This job listing has expired and the position may no longer be open for hire.

QA Technical Writer at Global Widget in Tampa, Florida

Posted in Writing/Editing 30+ days ago.

Type: Full-Time





Job Description:

It's time you found a career with an employer that values your vital contributions. At Global Widget, we believe in taking care of our people so they can take care of our business. As a leading manufacturer of health and wellness supplements and Hemp-derived products, our goal is to promote healthier lifestyles globally through natural solutions.

Position Summary/Objective

As part of the company’s Quality team, you will be a key member managing production and quality documentation.  The QA Technical Writer will be responsible for writing technical documents including but not limited to batch records, investigations, and risk assessments. 

Essential Functions


  • Determine the clearest and most logical way to present information for greatest reader comprehension.

  • Generate innovative ideas for process improvements.

  • Create and update GMP documentation including but not limited to batch records, manufacturing investigations, and risk assessments.

  • Must be able to create technical documents in both English and Spanish.

  • Meet with subject-matter experts to ensure specialized topics are appropriately addressed.

  • Analyze information required for the development or update of procedures and other documentation, as required.

  • Review and/or edit documentation developed by other departments.

  • Support the corrective actions as result of CAPA.

  • Other duties as assigned by management.

Required Skills and Experience


  • BILINGUAL - Must be able to read, speak, and write in English AND Spanish

  • Bachelors degree and/or 1-3 years of experience in a similar role

  • Excellent writing skills with a strong command of grammar, punctuation, and style.

  • Computer knowledge; proficiency with Microsoft Office Suite: Outlook, Word, Excel, PowerPoint

  • Strong people skills, good communication

  • Experience working in a cGMP manufacturing organization

  • Attention to detail is important and strong problem-solving skills.

  • Ability and willingness to change direction and focus to meet shifting organizational and business demands

  • Ability to demonstrate integrity, effectively manage oneself, be productive under pressure, and achieve personal and department goals





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