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Establish and maintain a document control system for engineering documents related to commissioning activities, ensuring accuracy, compliance, and version control. Collaborate with teams to collect and disseminate relevant documents. Implement quality control processes and provide training to team members. Stay current with industry standards and best practices.
Ensure suppliers deliver quality parts, materials, and services in the Pharmaceutical & Medical Devices Industry. Develop and maintain supplier quality standards, conduct audits, and resolve supplier-related issues. Bilingual in Spanish and English with strong problem-solving and communication skills.
Create detailed project plans, lead cross-functional teams, track project progress, manage budgets, build relationships with stakeholders, and ensure compliance with industry standards.
Provide oversight for the development and maintenance of quality programs, systems, processes, and procedures ensuring compliance with policies and performance. Lead audit and inspection preparation and liaise with regulatory agencies. Coordinate legal requests and drive process improvement efforts.
Assist in architectural design projects by preparing design concepts, drafting and modifying architectural drawings, conducting research and analysis, collaborating with senior architects, interacting with clients, supporting construction administration, and staying updated with architectural trends.
As a Process Engineer I, you will recommend and implement equipment and process modifications to meet quality standards and improve production efficiencies in the Pharmaceutical & Medical Devices Industry. You will also lead innovation, development, and optimization of new manufacturing concepts and processes. Bilingual in Spanish and English is required.
Recommends and implements equipment and process modifications to meet quality standards and improve production efficiencies in the Pharmaceutical & Medical Devices Industry. Leads innovation, development, and optimization of new manufacturing concepts and procedures. Develops manufacturing processes applicable to statistical process control. Collaborates with product design and development personnel to ensure compatibility with processing methods.
Leads cross-functional teams to manage projects for new product development and ongoing lifecycle management. Oversees operational aspects, manages project development and implementation, reviews project status, and resolves project issues to meet goals and objectives. Communicates with stakeholders to ensure project success.
Develop, modify, apply, and maintain quality standards and protocols for processing materials in the Pharmaceutical & Medical Devices Industry. Collaborate with engineering and manufacturing functions to ensure quality standards are met. Conduct quality assurance tests, perform statistical analysis, and implement corrective measures.
Seeking a Process Development Scientist with 5 years of experience in a Biopharmaceutical Environment. Responsibilities include conducting experiments, analyzing data, and troubleshooting technical problems related to container defects and packaging materials.
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