Seranbio

Seran is seeking a Quality Assurance Specialist to support the daily activities of Serán’s Quality Assurance department supporting GMP clinical manufacturing operations. This individual will be responsible for reviewing and approving raw material records, production records, investigations/CAPA, and

Serán BioScience is searching for an experienced Quality Control Scientist II to support an extended manufacturing schedule. This role would support all testing functions for Quality Control, primarily focused on in-process control lab methods to ensure manufacturing excellence. The Scientist II nee

Serán BioScience is looking for a scientist with laboratory experience to support manufacturing of pharmaceutical drug products within our In-Process Control group. As a scientist within the Quality Control department you will work alongside a team of scientists and operators to ensure the highest q

The Quality Control Supervisor for the In-Process Control (IPC) team supervises the Laboratory Analysts to meet testing requirements in support of the manufacturing schedule. This position works closely with QC Managers to ensure that policies and procedures are followed as written, and revised when

The Quality Control Supervisor for the In-Process Control (IPC) team supervises the Laboratory Analysts to meet testing requirements in support of the manufacturing schedule. This position works closely with QC Managers to ensure that policies and procedures are followed as written, and revised when

This role serves as the leads the Manufacturing Sciences and Technology (MSAT) team to oversee the transfer of robust, GMP-compliant manufacturing processes into Serán’s facilities for clinical and commercial production. As a critical member of the Commercial Steering Committee, this role will initi

Serán is seeking an Engineer Associate or Engineer I to support validation activities associated with pharmaceutical manufacturing equipment, utilities, computerized systems, facilities, and processes. This position is a crucial role in maintaining, scheduling, and executing qualification and valida

Validation is a regulatory requirement and must be conducted in conformance to cGMPs and FDA requirements. The Validation Technician or Specialist I will be part of a cross functional team that will execute validation studies for process, cleaning, computerized systems, and qualification of equipmen

Serán BioScience provides optimized drug development and manufacturing services from discovery through clinical stages. An expansion is currently underway to provide commercial manufacturing capabilities in 2027. The company uses a science-driven approach, combining predictive design tools, advanced

The Director, Commercial Quality Control is responsible for leadership, oversight, and strategic direction of Quality Control operations supporting commercial and late-stage clinical manufacturing. The role ensures that laboratory activities, analytical testing programs, personnel, systems, and faci

The cGMP Training Program Manager is responsible for managing and continuously improving the organization's GxP Training Program to ensure personnel are trained, qualified, and capable of performing assigned responsibilities in compliance with applicable regulatory requirements and internal Quality

Serán is seeking an Associate Director, Quality Compliance who will be responsible for leading the Quality Compliance program to ensure ongoing adherence to applicable GxP regulations, client requirements, industry standards, and internal Quality Management System (QMS) requirements. This role serve

Serán is expanding the Spray Dry Manufacturing Operations capabilities into a swing shift to support daily activities for the Operations Department. This Operations Supervisor will oversee swing shift activities according to established procedures focusing on spray dry dispersion manufacturing sched

Serán is seeking a Staff Accountant (AR Emphasis) who will be responsible for managing the company's billing and AR process, ensuring timely and accurate invoicing, collection of customer payments, account reconciliation, and maintenance of customer records. This position plays a critical role in pa

Serán is seeking a Manufacturing Production Planner who will be responsible for developing, maintaining, and optimizing the production schedule for GMP manufacturing activities. This role coordinates cross-functional activities to ensure manufacturing campaigns, material availability, equipment read

Serán is seeking a Quality Control Specialist with Instrumentation experience who will be responsible for managing laboratory equipment lifecycle and associated systems including planning, implementation, ongoing support, upgrades, maintenance, and system retirement. This person will develop and mai

Serán is seeking a Senior Controls & Calibration Technician to serve as the site subject matter expert (SME) for instrumentation, control systems, and low-voltage electrical systems supporting pharmaceutical development, laboratory operations, manufacturing processes, facility utilities, and future

Serán BioScience is looking for dedicated individuals who are looking to learn how to become Operations Technicians and Operations Specialists. You will play an integral role in operating and maintaining specialized equipment for the manufacturing of medicine for the use of early phase clinical FDA

Serán is seeking a Quality Assurance Senior Specialist who will be responsible for performing the day-to-day tasks of the QA Department supporting a GMP facility manufacturing, storing, and testing pharmaceutical products. Primary responsibilities include overseeing Supplier Quality, Auditing (suppo

Serán is seeking a Scientist II who will support the development, optimization, and validation of analytical methods used to characterize small molecule drug products for early and late phase clinical R&D to support client GMP Clinical Release and Stability programs. The work performed in this role