Jobs at LanceSoft

The Quality Assurance Professional will support the QA team in manufacturing processes, focusing on compliance, data analysis, and reporting.

Responsible for preparing high-quality FDA labeling documents, proofreading inserts, maintaining labeling materials, and understanding FDA regulations.

Designs and administers compensation plans and policies, ensuring alignment with business goals, and supports Total Rewards team in integration activities.

The Quality Assurance Specialist will oversee contract manufacturing operations and provide QA support for biologics products, ensuring compliance and quality standards. Responsibilities include documentation review, interfacing with laboratories, and tracking quality metrics.

Support clinical supply packaging operations, ensuring compliance with current Good Manufacturing Practices and providing guidance on necessary procedures and training.

The role involves supporting Post Market Regulatory Affairs activities, including complaint handling, MDR submissions, technical evaluations, and regulatory reporting while collaborating across various functional teams.

Lead Quality Assurance resource for global computer validation projects, ensuring compliance with internal and external regulations through audits and documentation review.

The role involves tracking and verifying records, data entry, assisting with GMP report data analysis, and ensuring compliance with SOPs.

The Senior Program Manager oversees complex programs from concept to launch, ensuring all teams meet project goals, manage resources, and communicate effectively with stakeholders.

The RF Engineer will design and deploy cell sites, conduct link budget analysis, site design, and collaborate with minimal supervision.

The Communication Specialist III will manage project communication and branding, develop materials for various stakeholders, and implement communication plans over multiple projects.

The Software Test Engineer will develop and maintain automation tools for software testing and deployment, ensuring efficient build and release processes.

The Paralegal will manage correspondence with outside counsel, prepare trademark documents, review service notices, and assist in research and due diligence.

The Workday HRIS Analyst III will provide system support and guidance, troubleshooting Workday issues and collaborating with HR users on organizational updates.

The Senior Associate, PV Documents is responsible for developing and delivering procedural documents to ensure regulatory compliance in pharmacovigilance, collaborating with internal teams and managing project timelines.

The Senior Quality Engineer leads quality engineering functions for product development, ensuring compliance and quality assurance in the medical device industry.

Leads training and change initiatives, manages the Education & Training Pillar, and develops training plans for employees. Coordinates training activities and ensures change management strategies are effective.

The Procurement Specialist is responsible for supporting Procure-to-Pay inquiries, managing supplier relations, ensuring compliance, training users, and driving process improvements.

The MySQL Database Administrator will plan, deploy, and maintain database systems, optimize performance, ensure security, and troubleshoot issues while collaborating with teams and customers.

Responsible for managing clinical data through the study lifecycle, identifying data issues, and ensuring timely delivery of data management tasks.