Pharma Positions Available in FL! Give me a Call! (Miami)
Protected content great Medical Devices company located in South Florida is looking for several positions. If you have background on any of the following fields or know someone interested, please send me a txt or give me a call! Thanks, Javier
In cases of new product implementation, prepares a Master Implementation Plan containing all specs, drawings, documents, equipment, material components and lead-times; and works with the Head of the different departments in getting all functional areas involved to commit to a plan that addresses marketing requirements in a timely fashion.
This position will be responsible for performing the necessary engineering development tasks, including investigation, invention, prototype, design (including detail drawings, structural analysis, tolerance analysis, etc.), testing, and validation bringing new and or existing technology to bear on product and design.
PMO Project Manager
The PMO Project Manager will provide strategic support to a suite of cross functional projects to ensure all strategic projects are managed and delivered as expected. This role requires working closely with all departments within the company to ensure project deliverables are achieved in a timely manner following a consistent delivery process. This management support role will be responsible for interpretation and distribution of project information, process ownership, process improvement, and establishing best practices and processes in the PMO.
Manager Quality Assurance QMS & Release
Responsible for Quality related business systems (QMS) such as NCR, OOS, Complaint, Deviation/CAPA, by contributing and reviewing for approval and assisting with the implementation and supporting on-going continuous improvements.
QA Manager PD
The Quality Assurance Manager will be responsible for quality operations related to Process Development (PD) such as written procedures including but not limited to: monitor and control the testing and production process development, qualification and validation. Additionally provide QA oversight to design assessment and design verification. Support investigations, and monitor compliance with all applicable requirements of good manufacturing practice.
QA Engineer Device Development
Primary responsibility to develop and execute activities related to quality in design and development of programs in the US Design Office. Supports their colleagues by providing the assistance required to meet overall quality objectives in all phases of product development in compliance with operating procedures.
Engineer, Analytical Sciences
Execute tests, document & analyze test data, write protocols, procedures, equipment work instructions, test instructions.
Senior Regulatory Affairs Specialist
Provide leadership and submission strategy in the preparation and filing of CMC sections of regulatory submissions and interactions with regulatory agencies (directly or with customers) for Pharmaceutical/ Device Combination Products.
Supervisor Quality Control will directly oversee QC personnel and perform, inspection and testing of materials, parts, and products to ensure adherence to established quality standards. The QC supervisor is also responsible for proper administration, maintenance and condition of QC test equipment / processes
Document Control Specialist
Maintain controlled spreadsheets, master lists of documents and up to date files for the following Quality Systems: Change Order (ECO), Suppliers (Reports, Lists, SCARs), Quality Operating Procedures (QOP’s), Batch Records, Drawings, (DWs) Quality Work Instructions (QWI’s), Investigations and Corrective Action and Preventive Action (CAPA), Audits, Training, Design History File (DHF), External documents, and Complaint Handling.