Senior Manufacturing Associate I/II (Nights) - Downstream
Job in
Durham, Durham County, North Carolina, 27703, USA
Listed on 2026-08-05
Listing for:
KBI Biopharma, Inc.
Full Time
position Listed on 2026-08-05
Job specializations:
-
Manufacturing / Production
Pharmaceutical Manufacturing, Manufacturing & Industrial Operations
Job Description & How to Apply Below
USA - NC
- Durham
- Hamlin Rdtime type:
Full time posted on:
Posted Todayjob requisition :
R
** JOB SUMMARY
**** Night shift: 7PM-7AM, 2-2-3 rotating schedule
** The
** Senior Manufacturing Associate I/II (Nights)
** is responsible for performing upstream or downstream processing of bulk intermediates and/or bulk drug substances for biopharmaceutical products. The Sr. Manufacturing Associate must follow written, approved procedures and forms to ensure all work is conducted “Right First Time” (RFT) following Good Manufacturing Practice (GMP), including good documentation practices, and/or Good Laboratory Practice (GLP). As needed, the Sr. Manufacturing Associate will work individually or on teams to author standard operating procedures (SOPs) or Master Batch Records (MBRs);
write corrective and preventive actions (CAPAs); and specify, commission, and qualify new equipment.
The Sr. Manufacturing Associate will be responsible for upstream unit operations (seed expansion, bioreactor operations, cell culture harvest), downstream unit operations (chromatography, tangential flow filtration, viral inactivation, and bulk filling) and/or manufacturing support operations (solution preparation, assembly preparation, parts wash, and autoclave) activities. The Sr. Manufacturing Associate will have past experience and a working knowledge of upstream processing equipment (incubators, biosafety cabinets, bioreactors, cell counters, blood gas analyzers, metabolite testing equipment), downstream processing equipment (mixing vessels, chromatography, tangential flow filters, virus filters), and/or manufacturing support equipment (mixing vessels, parts washers, and autoclaves).
Additionally, the manufacturing associate will have knowledge of general bioprocessing equipment such as filters, filter integrity testers, balances, pumps, pH/conductivity meters, and disposable technologies (disposable bags, sterile tubing welders, tubing sealers).The Sr. Manufacturing Associate will use past experiences and knowledge to teach, troubleshoot and continuously improve the daily operations of upstream or downstream manufacturing. Staff will maintain a sense of ownership of the production processes, the manufacturing environment, and the facility.
The Sr. Manufacturing Associate will execute daily tasks and maintain strict accordance with manufacturing records, SOPs, and GMP with minimal supervision and effectively communicate with the manufacturing supervisor and support groups. Staff will work cross-functionally with QA, MS&T, facilities, engineering, supply chain, IT, AFS, and other key departments to ensure startup and ongoing manufacturing operations are successful, reliable, and compliant.
The Sr. Manufacturing Associate will also be expected to review the manufacturing schedule, executed manufacturing documentation, and ERP orders to ensure compliant operations and schedule adherence. Staff will effectively communicate questions, concerns, or deviations to management and the quality system according to KBI internal notification processes.
** JOB RESPONSIBILITIES
*** Manufacture bulk intermediates and drug substances per manufacturing batch records and in compliance with quality standards, company policies and current regulations.
* Perform operations in a cleanroom environment, applying controls to ensure aseptic processing including gowning and cleaning procedures
* Document each task involving manufacturing records and logbooks following GDP at the time of execution.
* Utilize and perform maintenance on equipment per applicable SOP.
* Ensure all materials are issued and accounted for during the execution of a record (i.e. SR, EPR and ).
* Demonstrate, apply, and ensure understanding of cGMP and how it applies to specific tasks and responsibilities.
* Participate and be accountable for workplace organization (5S).
* Provide direction/guidance to Manufacturing Associates. Help supervisor to distribute the workload and ensure others understand the requirements of their tasks.
** MINIMUM REQUIREMENTS
** Sr. Manufacturing Associate I:
* Bachelor’s degree in a related…
Position Requirements
10+ Years
work experience
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