Pharmaceutical Technical Writer

4 days ago


Miramar FL United States ttg Talent Solutions Full time

Technical Writer

Miramar, FL

On-site

Contract


DESCRIPTION:

Are you a detail-oriented Technical Writer with a passion for creating and revising company documents? We are seeking a talented individual to join our team. In this role, you'll be instrumental in formatting, writing, and enhancing critical documents for various departments, focusing on SOPs and other company materials. As a Technical Writer, you will collaborate with multiple teams to support documentation needs, particularly for system transitions and on-site requirements.


RESPONSIBILITIES AND DUTIES:

  • Write and revise departmental documents, such as Batch Records, Work Plans, Addendums, Forms, Checklists, SOPs, Knowledge Checks, Answer Keys, and Qualification Checks.
  • Provide assistance to all departments for their documentation requirements.
  • Manage multiple assignments concurrently, working both independently and as part of a team.
  • Produce error-free documents within specified timeframes.
  • Select and incorporate relevant photographs, drawings, and diagrams to enhance document usability.
  • Coordinate tasks related to typing, change control, copying, training, and document distribution.
  • Ensure that documentations meet triennial review dates.
  • Track and communicate the status of document changes.
  • Collaborate with the Department Trainer/Coordinator to ensure department training requirements are met.
  • Support the training team with training documentation entries, particularly during high-peak entry periods, such as Annual GMP training.
  • Work harmoniously within a team to achieve collective goals.
  • Perform all work in alignment with our core values: Innovate, Evolve & Excel.
  • Execute any other relevant duties as assigned.


REQUIREMENTS:

  • 1-3 years of direct job-related experience.
  • A college degree (B.S. or B.A.).
  • Proficiency in current Good Manufacturing Practices (cGMP).
  • Understanding of pharmaceutical principles, practices, and applications.
  • Strong mathematical and statistical skills.
  • Familiarity with documentation practices and principles.
  • Excellent command of business English, including usage, spelling, grammar, and punctuation.
  • Effective written and spoken English communication skills for clear interaction with all company employees.
  • Computer literacy with proficiency in Microsoft Office programs. Exposure to SAP, QMS, and other systems is a plus.
  • Skills in researching, reading, interpreting, and writing technical documentation, effectively merging company and compliance regulations into Standard Operating Procedures.
  • Demonstrated ability to manage multiple priorities in a fast-paced environment.
  • Proven experience in systematic problem solving.
  • Capability to work effectively within a team environment, as demonstrated through previous work experience.


At ttg, “We believe in making a difference One Person at a Time,” ttg OPT



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