| Location | Fremont, CA |
| Salary | $53,600–$80,400 Per Year |
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MFG Associate OR Senior Associate, Upstream, ONSITE, Fremont CA, SWING SHIFT
Description
Executes routine unit operations in Upstream manufacturing as assigned related to the manufacturing of bulk drug substance in a multi-product facility. Performs duties under limited supervision and according to standard operating and manufacturing procedures. As an employee of Boehringer Ingelheim, you will actively contribute to the discovery, development and delivery of our products to our patients and customers. Our global presence provides opportunity for all employees to collaborate internationally, offering visibility and opportunity to directly contribute to the companies' success. We realize that our strength and competitive advantage lie with our people. We support our employees in a number of ways to foster a healthy working environment, meaningful work, mobility, networking and work-life balance. Our competitive compensation and benefit programs reflect Boehringer Ingelheim's high regard for our employees.
This is a swing shift Position: Wednesday 3pm - 11:30pm, Thursday - Saturday 3pm - 1:30am.
Duties & Responsibilities
Executes, with oversight of qualified staff, complex unit operations including but not limited to batching and inoculation of bioreactors, operation of bioreactors, process monitoring, and harvest operations.
Executes independently with adequate training fundamental operations:
CIP/SIP of bioreactors, tanks, and harvest equipment.
Media preparation and transfer into tanks and disposables.
Cell inoculation and transfer.
Daily analytics and maintenance of analytical equipment.
May be required to support parts cleaning and weigh and dispense operations.
Performs internal support duties including stocking consumables/materials, updating controlled SOP binders, appropriately discarding expired reagents, recognizing and reporting process and equipment anomalies.
Documents work according to cGMP and cGDP.
Adheres to established regulations and follows cGMP established by site.
Reports abnormalities and deviations in a timely and accurate manner.
Adheres to safety standards and identifies unsafe situations / habits and escalates appropriately.
Maintains production areas according to predefined standards (5s).
Maintains own training within compliance and trains other technicians and associates on operations upon completion of trainer qualification.
Contributes to Quality activities as investigations and area walk-throughs.
Requirements
Compensation Data
The base salary range for this position is $53,600 to $80,400 OR $65,400 to $98,000. The position may be eligible for a role specific discretionary bonus, relocation, and/or other compensation elements. We continuously review market data and may adjust salary ranges as needed in the future. Actual compensation will be based on job-related factors such as skills, experience, and qualifications, and other factors permitted by law. For an overview of our benefits please click here.
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