Key Responsibilities. Perform independent and thorough review of QC microbiology data for completeness, accuracy, and cGMP compliance. Verify raw data, calculations, instrument outputs, electronic records for assays including but not limited to bioburden, sterility, endotoxin, media qualification, and environmental monitoring. Confirm adherence to SOP’s, test methods, and approved protocols. Ensure documentation meets ALCOA data integrity princip...
Title: Biomanufacturing Technician. Location: Memphis, TN. Duration: 6 months (contract to hire). NOTE: Training will be provided & must be able to work at night, weekends, and holidays. Shift. 6-6:30pm/ once trained potentially moved to 10:30am-11pm. Training is 6-8 weeks. Schedule. 2nd Shift: 10:30am-11:00pm (2 shifts on, 2 shifts off, 3 shifts on, 2 shifts off, 2 shifts on, 3 shifts off with the 3-days falling Friday – Sunday). Built in OT bas...
Title: Rhapsody Developer. Location: Lansing, MI 48915 (Hybrid: Onsite days are Wednesdays and Thursdays). Job Duration: 12 months (High possibility of longer extensions). Shift: Mon – Fri (8:00 AM – 5:00 PM EST). Job Description. Overview. . This position is for Software Solution Architect who will support and complete the tasks necessary to design and implement a methodology to enable the Client Health Services ESB to track the transmission of ...
Title :Clinical Study Associate II. Location -Cambridge MA -Remote. Duration -8 months. Duties. What You’ll Do. Support the Clinical Operations Study Leader and team in managing and overseeing clinical trials. Reports to an Associate Director of Clinical Operations (or above). Responsibilities. Assist in day-to-day trial execution: site start-up, enrollment, monitoring, and data flow. Prepare study documents (consent forms, site instructions, man...
Duties. Participates in the day-to-day supervision of clinical trial execution, with a focus on site start up, patient enrollment, monitoring, and data flow metrics from the clinical sites, CROs and central labs. Supports complex clinical trial activities in support of the Clinical Study Manager and other team members. Prepare study documents (i.e. consent forms, site instructions, study specific materials such as the Manual of Operations, Pharma...
Job Title: Senior Clinical Study Associate III. Site Location: Cambridge, MA. Duration: 06 months (possible extension. Schedule Notes: Hybrid, 3 days per week onsite. Pay rate range: $80 - $86/hour on W2. Job Description. Participates in the day-to-day supervision of clinical trial execution, with a focus on site start up, patient enrolment, monitoring, and data flow metrics from the clinical sites, CROs and central labs. Supports complex clinica...
Job Title: Photo Coordinator. Location: New York, NY. Duration: 05 Months (Possible Extension). Job Description. The client’s photo department is looking for a Photo Coordinator to join the team in the New York office. Reporting to the VP of Photography, this role will support the Client Streaming Photo team across a wide range of responsibilities. This role will work closely with the team to manage the photography across unit coverage and market...
Title: Sr. Microbiologist. Location: SLC, UT. Duration: 12 Months. Job Description. Responsibilities associated with this Sr. Microbiologist position include working with corporate and various Client's sites interpreting microbiological testing data, monitoring, and providing remediation support for the sterility assurance program used in medical device manufacturing. The candidate must have experience interpreting and applying standards and regu...
Title: Sr. Microbiologist. Location: SLC, UT. Duration: 12 Months. Job Description. Responsibilities associated with this Sr. Microbiologist position include working with corporate and various Client's sites interpreting microbiological testing data, monitoring, and providing remediation support for the sterility assurance program used in medical device manufacturing. The candidate must have experience interpreting and applying standards and regu...
Role: Cell Therapy Specialist I / Manufacturing AssociateLocation: Frederick, MD 21704 - onsiteDuration: 05 Months Shift: 1st shift 6:00 am to 4:30 pm (Day Shift), Sun-Wed and 2nd Shift Wed-Sat & 3:00 pm to 1:30 am (Swing Shift), Sun-Wed and Wed-Sat Role is full time 4/10 role but the roles and shifts can change with the needs of the dept. Shift times will be directed by the manager or dept leads.Pay Range: $28 to $30 hourly on W2Position: 10 Pos...
Role: Cell Therapy Specialist I / Manufacturing AssociateLocation: Frederick, MD 21704 - onsiteDuration: 05 Months Shift: 1st shift 6:00 am to 4:30 pm (Day Shift), Sun-Wed and 2nd Shift Wed-Sat & 3:00 pm to 1:30 am (Swing Shift), Sun-Wed and Wed-Sat Role is full time 4/10 role but the roles and shifts can change with the needs of the dept. Shift times will be directed by the manager or dept leads.Pay Range: $28 to $30 hourly on W2Position: 10 Pos...
Key Responsibilities. Perform independent and thorough review of QC microbiology data for completeness, accuracy, and cGMP compliance. Verify raw data, calculations, instrument outputs, electronic records for assays including but not limited to bioburden, sterility, endotoxin, media qualification, and environmental monitoring. Confirm adherence to SOP’s, test methods, and approved protocols. Ensure documentation meets ALCOA data integrity princip...
