Top Biotech Jobs

The Process Expert provides technical support for manufacturing processes, oversees investigations for deviations, leads process improvements, and trains team members in compliance with guidelines.

Support the leadership team in data-driven decision-making by synthesizing data insights and collaborating across functions to drive business growth and improve enterprise strategies.

The Engineering Specialist will execute engineering activities, perform maintenance on equipment, guide team members, and ensure adherence to quality policies.

Lead end-to-end execution of aesthetic product programs from concept through commercial launch. Maintain integrated project plans, drive cross-functional alignment, manage external partners, support regulatory submissions and international expansion, track program health in PM tools, and communicate status to leadership.

Support the PMO by coordinating document reviews and approvals across cross-functional teams, maintaining project trackers/databases, monitoring status and due dates, and flagging risks to ensure on-time completion.

The Inside Sales Training Specialist will design and implement training programs for the Patient Services team to enhance productivity and improve patient experience. Responsibilities include identifying training needs, delivering programs, tracking training effectiveness, and collaborating with cross-functional teams.

Support commercial CMO manufacturing data analysis for Carvykti: collect and analyze CPP, in-process, and release data; track KPIs; perform statistical and root-cause analyses; build dashboards, reporting, and CPV analytics; optimize data architecture and deploy predictive modeling to improve process performance.

Lead end-to-end program management for preclinical through clinical development programs, owning integrated plans, timelines, risk mitigation, and governance. Align cross-functional stakeholders, prepare executive presentations, and drive decision-ready execution using program management tools and best practices to advance small-molecule drug candidates toward IND/CTA and clinical milestones.

The Associate Director will lead programming and quality review using SAS, collaborate with various teams, and manage project timelines for clinical trial data.

Perform routine reagent production and cell culture tasks under supervision, operate and maintain lab equipment, document work, follow safety/biohazard procedures, stock reagents, and assist with assigned laboratory and QA/STM duties during training.

Lead QA Technical Operations for clinical and commercial biologics manufacturing: define cGMP standards, oversee QA MES, validation oversight, and tech transfer; ensure audit readiness, present quality metrics, allocate QA resources, and maintain regulatory compliance.

The role involves analyzing genetic and phenotype data, developing statistical tools, and collaborating to connect genetic variation with human diseases.

Lead and manage IT/OT operations in a GxP-regulated environment, ensuring reliable infrastructure (servers, networking, WiFi), compliance with FDA standards, integration of IT and OT systems, vendor management, disaster recovery, and performance reporting while mentoring a technical team.

Lead the development of facility-level analytics and sales strategies for the Long-Term Care sales force, optimize operations and support digital sales effectiveness.

Oversee daily administrative and operational functions of a clinical research site, ensure compliance, manage HR activities, develop budgets, monitor financial/operational metrics, and execute business strategy to meet organizational goals.

Provide clinical nursing support for research participants, execute study protocols, collect and document data, perform vitals and specimen handling, assist with investigational medication administration, obtain informed consent, monitor adverse events, maintain study logs and supply inventory, and ensure compliance with GCP, FDA, and site SOPs.