Responsible for independently coordinating all activities associated with timely packaging, labeling and assembly of clinical materials for designated domestic and international studies in ...
SCOPE OF SERVICES Influence the enhancement, implementation, and execution of the requirements management process and plan, including elicitation, analysis and verification strictly as a ...
ROLE SUMMARY: The position is responsible for maintaining adherence to the Integrated Manufacturing Excellence (IMEx) standards for continuous improvement (CI). Primary responsibilities ...
Responsibilities: Support the Net Metering Team by, Maintaining, Reviewing And Tracking The Net Metering And Interconnection Application Enrollment Processes for distributed generation and ...
Position Overview: The ECQ Equipment Engineer supports the successful operation of facility, laboratory and business functions at their home site through interaction with internal ...
To perform any process/support duties associated with the automated filling of vaccines. Works within the filling department as a team member to ensure success in the activities associated ...
DIRECT HIRE - NO INERVIEW - START ASAP SHIFT 1 M-F 1PM to finishShift 2- M-F 3PM to finishShift 3 - M-F 600AM– 3PM Pay: $14/hr On W2 Under general supervision of the Operations ...
Authoring and resolution of deviations in order to meet production and product release requirements. Identification and facilitation of interdepartmental process improvements. Utilize root cause ...
Quality Control Validation Scientist I is responsible for the qualification activities, following SOPs and regulations including Data Integrity, related to one or more of the following areas: ...
Responsible for project management support for Oncology Field Medical team. Support key initiatives and events and support OFM organization communication and non-therapeutic training ...
1 nurse from 7-41 nurse from 4-11Would need to be open to weekends**These will be primarily used to help screen employees as they are entering the plant for COVID-19 reasons.**Could go up to 3 ...
Responsiblites: Collaborate within and across Cient functions with appropriate disciplines to identify and ensure management of internal and external documentation and support when ...
CORE JOB RESPONSIBILITIES: Job Description: Clinical Research Scientist Review of clinical data within eCRF system, patient profiles, etc. to issue queries and clean data from clinical ...
Department Description: The Clinical Trial Business Partnering (CTBP) department is focused on executing the business’ sourcing strategy across all phases of R&D development operations. ...
Need up to 10 contractors depending on shifts that they choose 6-8 contractors from 5:00 am - 8:30 am 2-3 from 1:30 pm - 7:00 pm Monday - Friday and every other Saturday If someone is willing to work ...
6AM to 6PM, 36 hr, 48 hr rotation OR 6PM to 6AM, 36 hr, 48 hr rotation Essential Job Functions:• Follow all Food Safety (HACCP), GMP’s, Occupational Health and Safety, ...
Background: The Device Development department is searching for a dynamic Device Engineer to bring innovative drug delivery devices into clinical and commercial production to support next-generation ...
This position will be responsible for uploading regulatory documents to the electronic Trial Master File and Product Files, implementing document workflows and tracking through to completion.This is ...
Administrative Support Schedule and file AWARE frequency reports Schedules Safety Data Review meetings and attends as able Applies medical, life science and general scientific knowledge and ...
Working under direction, the Associate Manager of Medical Information will respond, verbally and in written format, to medical inquiries from healthcare professionals, patients, and consumers (or, at ...
