Responsible to review Bioanalytical data and electronic lab notebook documentation to ensure accuracy and integrity of data Perform detailed document quality review of protocols, method development reports and study reports to verify integrity of data in support of regulatory submission Ensure Good Research Practices are observed within Bioanalytical Operations Collect me

Reviews master batch records and provides customer approval for quality tasks for externally manufactured products Performs final review of executed batch and/or critical systems documentation and determines acceptability by using standard operating procedures Ensures presence and acceptability of all required documentation prior to the release of the product and/or syste

Associate Scientist II Analytical Development Category Life Science Employment Type Direct Hire Reference BH 357288 Associate Scientist II, Product Analytical Development 100% Onsite in Lexington, MA Direct Hire Salary range $95K $110K per year + Bonus Candidates coming from a gene therapy, drug product development environment along with experience developing, qualifying,

Determines systems specifications based on business requirements, working with business end users to elicit proper solution design Works to integrate/implement systems solutions working with development, quality, and release teams Produces systems delivery specifications, technical systems design, user procedure documents, training documents, and rollout procedures, as ap

Design and development of equipment, processes, and control systems, used for production and assembly of cell encapsulation devices. Manage the evaluation and selection of new equipment/technologies or modifications to existing systems to consider new processing technologies. Support ongoing optimization and improvement in equipment/systems/processes for long term robustn

R&D Engineer II Systems Category Engineer Employment Type Contract Reference BH 356931 Staff Engineer R&D Verification and Validation needed for a 12 month contract opportunity with Yoh's client located in Andover, Massachusetts. About the Job The Staff Engineer, R&D Verification and Validation, is the technical lead in the design verification or design validation of elec

The Clinical Supply Chain Senior Coordinator is responsible for a wide variety of administrative activities within Clinical Supply Chain. Activities typically consist of well defined support tasks that are performed independently as well as projects of increased complexity completed under moderate limited supervision. Key Duties and Responsibilities Coordinates with exter

SCIENTIFIC COORDINATOR Category Life Science Employment Type Contract Reference BH 357234 This position is of scientific coordinator. Chosen candidate will be responsible for facilitating assigned selected aspects of laboratory processes, which may include workflow, quality control process, performance improvement activities, training of new employees, advanced problem so

Appointment Scheduler Category Administration & Office Support Employment Type Contract Reference BH 356085 1 Appointment Scheduler needed for a long term contract assignment with YOH's client located in Burlington, MA. This healthcare organization provides a comprehensive health team which is dedicated to help the people find the information and care they need to live li

Medical Receptionist Category Administration & Office Support Employment Type Contract To Hire Reference BH 356086 1 Medical Receptionists needed for contract to hire positions with YOH's client in Multiple on site locations Needham, MA, Burlington, MA, Salem, NH, Amesbury, MA, Medfield, MA, Seabrook, NH, Newburyport, MA. This healthcare organization provides a comprehens

Primary responsibility for all phases of OATT/LGIP/SGIP study and process administration and coordination for multiple Requests Process management; monitor schedules and ensure timely completion per FERC requirements Application and Study processing & contract development Amended Interconnection Agreement coordination and management Coordination/direction of OATT/LGIP/SGI

Qualify QC equipment Design, execute, manage, and implement QC instrument/software qualification documents such as (but not limited to) User Requirement Specification (URS), Design Qualification (DQ), validation plans, equipment IOQ protocols, software test scripts, risk assessments, qualification summary reports Own change controls specific to the qualification of QC ins

Performs Quality Control of routine documents Document management and archival Provides management aspects of outsourced and internal projects including contracting and vendor management May perform administrative functions (scheduling internal and external meetings) Under direction of supervisor, participates in cross functional alignment initiatives May be responsible f

The responsibilities of this position may include, but are not limited to, the following Participates in cross functional teams as a Quality technical resource responsible for providing support to manufacturing operations at contracted suppliers Supports quality investigations /deviations and reviews corrective action plans for adequacy and compliance. This includes root

Platform Engineer Category Banking & Financial Services Employment Type Contract Reference BH 357102 Platform Environment Engineer with some Architecture This is a hands on technical role Keys SQL skills a must Cloud Kafka Mq Messaging Snowflake Intermediate skills Who we are looking for Looking for candidates to implement middle office investment accounting clients on a