Documentation Coordinator Position Available In Broward, Florida
Tallo's Job Summary: The Documentation Coordinator role at Actalent for a Pharma Company involves ensuring compliance with industry regulations, supporting various teams, analyzing data, preparing protocols, and creating technical documentation. Responsibilities include following company policies, collaborating with departments, managing approval processes, reviewing data, creating verification protocols, and utilizing systems like Empower and LIMS for data management. The role requires technical writing skills, document control, and adherence to quality standards, with a degree in Sciences or Engineering preferred. Additional skills in quality investigations, verifications, validations, and experience with QMS (Trackwise) are beneficial. The work environment is based in a high-end clean room facility, requiring integration with subject matter experts on the manufacturing floor.
Job Description
Actalent is Hiring a Documentation Coordinator for Pharma Company! Job Description The Documentation Coordinator ensures compliance with industry regulations and supports teams across research, development, production, and quality assurance. This role involves analyzing data, preparing protocols, and creating technical documentation to help projects run smoothly. Responsibilities Follow company policies, procedures, and safety standards, ensuring compliance with all regulations. Work with departments like R D, Production, Quality Assurance, Engineering, and Regulatory to support project goals. Prepare final reports and manage the approval process. Review data for raw materials, components, and products used in testing. Create verification protocols for testing methods. Support technology transfer evaluations. Review and approve lab work and data as assigned. Use systems like Empower and LIMS for data management. Conduct audit trail reviews in relevant software. Write and update standard procedures, specifications, and technical reports. Collaborate with team members to meet company objectives. Demonstrate company values in all tasks. Follow ethical and compliance standards. Prepare and assess stability protocols and reports. Develop and validate Excel-based calculations and formulas. Perform other related duties as needed. Essential Skills Technical Writing Document Control Quality Standards Degree in Sciences or Engineering Additional Skills & Qualifications Quality Investigations Verifications Validations QMS (Trackwise) Work Environment The role is based in a high-end clean room centric facility. You will have your own office space but will be required to integrate with subject matter experts on the manufacturing floor.
