Technical Writer / Trainer

Technical Writer / Trainer

Aveva Drug Delivery Systems

About Us

Aveva Drug Delivery Systems is a pharmaceutical manufacturer at the forefront of innovative drug delivery technologies. We are dedicated to advancing solutions that optimize the efficacy, safety, and precision of pharmaceutical treatments. Join our team and help shape the future of healthcare by contributing to the development of groundbreaking drug delivery systems that improve patient outcomes worldwide.

Job Details

Location : Tamarac, FL

Job Summary

The incumbent will provide documentation support for various Production, R&D and Technical Service functions as determined by project assignments. The position will work closely with Production members and outside departments to coordinate and facilitate the various needs of the department. Accomplishments will be objectively determined by the successful and timely completion of coordination and support activities, including documentation creation and implementation. The position exists to support the ongoing creation and execution of the product pipeline for the company.

Key Responsibilities

Responsible for creating and managing project documentation, including change control documents, raw material specification, forms, master batch records, protocols, and other documents as assigned to support Production needs.

Responsible for coordinating raw material and API orders with the Purchasing Department as required to support project needs.

Responsible for assisting with the procurement and tracking of raw materials, parts, and equipment, as needed for different projects.

Responsible for assisting with the communication of general R&D and Technical Services requirements to other departments.

Responsible for supporting or assisting with the activities relating to Production process and GMP batch preparation.

Responsible for operating in accordance with the company’s Code of Conduct and Business Ethics, and all established regulatory, compliance and safety requirements.

Other related responsibilities as assigned by Production management.

Major Duties

Creation of specifications for raw materials and supplies for Production projects, and collection of documents required to support raw material assessments.

Creation of Production, R&D and Technical Services documentation including Master Batch Records, Forms, Protocols, summaries, and other related documentation.

Procurement and tracking of materials, parts, equipment, and supplies supporting Production development projects.

Review and confirmation of the status of materials, parts, equipment and facilities, as needed for development projects.

Work with offsite groups to assist with the transfer of information to the Aveva site in support of Production Projects.

Assist with the preparation activities pertaining to Production process trials and GMP batch preparation, including materials requisitions, preparation of trial notebooks, and QA / Trackwise documentation.

Work with Project Management to assist with the alignment of Production needs and deliverables within the project.

Qualifications

Education

Bachelor’s degree from an accredited university in Biology, Chemistry, Engineering or similar field.

Knowledge, Skills and Abilities

Strong organizational and communication skills, ability to work effectively with internal and external team members and work effectively as a team member.

Ability to track project tasks and deliverables.

Strong writing skills and ability to write clear, concise, documents of a technical nature.

General knowledge of the pharmaceutical work environment, such as GMP and safety practices.

Computer skills including MS Word, Excel, PowerPoint, and other relevant software programs.

Experience

Bachelor’s degree and minimum of two (2) to four (4) years of pharmaceutical-related experience.

High school graduate, and six (6) or more years of pharmaceutical-related experience.

Benefits

Medical / Dental / Vision Insurance

Paid Time Off

401k with employer match

Paid Holidays and Floating Holiday

Equal Opportunity Employer

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