Alphanumeric is hiring a BIOPHARM MANUFACTURING ASSOCIATE Level 2 to work in King of Prussia, PA for our client of 20 years committed to improving lives through medical and pharmaceutical advancements.
This role requires full eligibility to work in the USA. We do not offer work visa sponsorships for this position.
Conditions:
- Type of employment: Contract W2, on-site
- MUST BE ABLE TO WORK with W2
- Duration: TBD
- Location: King of Prussia, PA
- Hours/Shifts: Training “Boot Camp” 4 weeks M-F (7:30am – 4:00pm EST) and then 12-hour shifts from (5:00pm to 5:00am OR 5:00am to 5:00pm EST) including every other weekend and Holidays | 3- or 4-day week with a rotating schedule.
- Pay range: 33$/hour
Key Responsibilities:
- As a Biopharm Manufacturing Associate II, you will perform production operations including fermentation or cell culture operations, preparation of solutions, chromatographic separation, filtration and concentration operations, autoclave and parts washing of process assemblies, and area cleaning/upkeep.
- Will be responsible for completing daily manufacturing tasks and increasing competency in different production areas over time.
- Will participate in safety and compliance initiatives, as well as investigations.
- Will engage in the GSK Production System to continuously improve safety, quality, and schedule/cost performance.
- Under the direction of senior personnel, the biopharmaceutical manufacturing associate II performs a
variety of large production operations, interacting with automated equipment and
monitoring/processing data. - Will be responsible for completing daily manufacturing tasks and increasing competency in different production areas over time. They will participate in safety and compliance initiatives, investigations, and help solve technical and organizational problems while working with different teams of experts.
- With good documentation and data integrity practices, safely and compliantly completes and documents daily manufacturing tasks per standard operating procedures, batch document instructions, and logbooks.
- Supports in cross-functional activities, such as engineering actions, validation actions and Tech Transfer actions, including proactive safety and compliance input prior to execution.
- Primarily these activities are within the production suite but sometimes require out-of-suite or off-site work (i.e. FAT support).
- Monitors equipment and critical process parameters and escalate any issues or abnormalities and participating in the resulting troubleshooting activities.
- Strives to maintain a high level of competency with current and emerging digital platforms (SAP, EBR, AR/VR, etc).
- By learning the production schedule and assessing it daily, proactively ensures all processing equipment and necessary materials are adequate and available to set the team up for success.
- Transparently participates in investigations that are the result of safety or compliance issues.
Basic Qualifications:
- BS/BA degree, with cGMP manufacturing experience.
- OR an Associate’s degree from Montgomery County Community College in Biotechnology or related technical field with cGMP manufacturing experience.
- OR High School degree, 1+ years of cGMP manufacturing experience.
- Open to any other scientific background education or experience.