Precision Medicine Group
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Jobs at Precision Medicine Group
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Join PRECISIONscientia's Talent Community to be considered for various roles in scientific communications, including Account Services, Creative, Program Management, and Writing/Editorial. You will receive updates on relevant roles and networking opportunities, as well as guidance on early career events, all while being a part of a team passionate about improving patient lives through science and strategy.
The Vice President, Digital leads digital strategy and project management efforts within Precision AQ, managing teams across digital development, UX design, and consulting. They drive innovation in healthcare through strategic initiatives, oversee digital projects, and ensure adherence to quality standards while mentoring stakeholders on digital best practices.
The Quality Assurance Specialist II will support onsite quality systems in a regulated laboratory environment, managing document control, conducting internal audits, and ensuring compliance with specifications and standard operating procedures. Responsibilities include quality inspections, release of materials, and mentoring personnel in best practices.
Join our Talent Community to express interest in career opportunities with Precision Medicine Group. This is not an official application, but a way for recruiters to know about your skills and experience for future positions.
The Quality Assurance Specialist III is responsible for overseeing GxP quality systems, managing audits, and ensuring compliance in a laboratory production environment. They handle document control, analyze quality system data, provide training, and lead departmental projects while acting as the quality lead in validation activities.
The Document Specialist II is responsible for preparing TMF plans, conducting document QC and indexing according to GCP and relevant regulations. This role includes managing document processes, monitoring submissions, and ensuring timely resolution of issues, along with handling close-out activities for clinical studies.
The SaaS Implementation Consultant will manage client implementations, configure solutions, and provide technical support in the life sciences industry. Responsibilities include developing automated workflows, training customers, and mentoring junior staff while engaging in strategic planning and project management.
The Data Stewardship Analyst will validate and enrich data content for Data Products, conduct primary and secondary research, support data governance strategies, and maintain data dictionaries while ensuring data quality and proper classification in collaboration with various teams.
The Associate Vice President, Group Account Director is responsible for managing client relationships and overseeing the delivery of marketing services and products. The role involves mentoring account teams, ensuring project quality, maintaining client satisfaction, and supporting business development initiatives. It requires significant experience in pharmaceutical advertising or medical communications, as well as strong leadership in client account management.
As a Sr. Analyst in Market Access Consulting, you will drive client-focused solutions by conducting detailed secondary research, facilitating interviews, and preparing well-organized presentations. Your analytical skills will help you derive insights to address client issues related to market access.
As a Consultant, you will engage in research, data analysis, and preparation of presentations for healthcare market access projects. Responsibilities include synthesizing insights, conducting both qualitative and quantitative research, and supporting business development activities while collaborating on multiple projects.
The Director of Business Development at Precision Bioservices is responsible for identifying and securing significant business opportunities, enhancing client relationships, writing proposals, managing project budgets, and expanding business partnerships within the pharmaceutical and biotech sectors.
The QA Manager oversees the quality assurance department, developing and maintaining quality systems for the Product Solutions team, collaborating with leadership to ensure effective product testing, and managing quality tasks across teams in both the US and India. Responsibilities include leading strategies for quality mindset, coaching staff, documenting bugs, and continuous assessment of quality processes.
As a Project Controls Engineer, you will support biomanufacturing projects by producing key deliverables such as budget estimates, project schedules, cost reports, and trend analysis. You will analyze project data and facilitate clear communication for decision making, while collaborating with clients and maintaining valuable relationships.
The Manager, Centralized Visit Report Reviewer leads and manages a team of Clinical Visit Report Reviewers to maintain quality standards, ensure compliance with regulations, and achieve performance goals. Responsibilities include mentoring team members, collaborating on operational improvements, and providing strategic oversight and support to optimize report management processes.
As a CQV Engineering Consultant, you will lead client project initiatives in the life sciences sector, providing hands-on support for engineering processes and equipment. You will develop technical documentation, mentor team members, and engage in business development through building professional networks.
The Technical Support Specialist will offer technical troubleshooting and support in a lab environment, ensuring uptime for machines and assisting users with Windows PCs, Microsoft 365, and various devices. Responsibilities include desktop support, troubleshooting, and creating user accounts while adhering to GLP practices.
As a Manager in CQV Engineering, you will lead high-performing teams executing manufacturing projects, ensuring client satisfaction, managing accounts, and providing technical direction. You'll develop strategies and oversee project delivery life cycles, focusing on continuous improvement and team growth within the life sciences industry.
The Project Engineer will align with cross-functional teams, provide support in the engineering lifecycle, author technical documents, execute validation protocols, solve problems, and build relationships while contributing to the organization's mission.
The Senior Project Engineer will support cross-functional teams in engineering processes, conducting validations, authoring technical documentation, and troubleshooting cutting-edge manufacturing equipment, while ensuring alignment with quality and operational standards.