Manufacturing Associate I/II
Durham, NC 
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Posted 3 days ago
Job Description
Position Summary
This position is on a 2-2-3 schedule, 7a-7p. The Manufacturing Associate I/II - Downstream is responsible for the execution of production activities for early and late-phase Cell Culture programs within a GMP environment.

Position ResponsibilitiesThe Manufacturing Associate I/II - Downstream must follow the instructions depicted in SRs, EPRs, SOPs and forms. Additionally, must ensure all work is conducted following Good Manufacturing Practices (GMP), Good Documentation Practices (GDP) and Good Laboratory Practices (GLP); including "Right the First Time' (RFT).The candidate will maintain a sense of ownership of the production processes, manufacturing environment and facility. They will be exposed to buffer solution preparation, purification operations, viral inactivation and filtration processes, ultrafiltration/diafiltration operations, aseptic technique and column packing; as well as to cell culture analytical tools and general biotechnology auxiliary equipment (pumps, pH/conductivity meters, SoloVPE, FIT).

Position Requirements
  • Basic knowledge of buffer solution preparation or purification processing is preferred
  • Experience in single-use platform technology is preferred
  • Excellent written and verbal communication skills are required
  • Energetic, motivated and dynamic individual.
  • Must be organized and able to focus in a fast-paced, multi-tasked environment and maintain operational efficiency and positive demeanor.

Salary: 24.03-36.05/hour

Salary range provided per current averages and expectations. The salary and job title for this opening will be based on the selected candidate's qualifications and experience and may be outside this range. KBI has a robust total rewards strategy which includes an annual bonus structure for all employees, medical, dental, and vision coverage, paid PTO and holidays, 401K matching with 100% vesting in 60 days and employee recognition programs.

KBI Biopharma, Inc. (KBI) is committed to providing a safe and healthy workplace. Any employee entering a KBI site located in the US must either (1) have provided proof of full vaccination (as defined by the CDC) with a COVID-19 vaccination which has been granted FDA approval or Emergency Use Authorization; or (2) perform weekly COVID-19 testing with negative test results.

KBI Biopharma, Inc. is an EEO/AA employer and actively seeks to diversify its work force. Therefore, all qualified applicants, regardless of race, color, national origin, religion, gender, gender identity, sexual orientation, age, disability or veteran status, are strongly encouraged to apply.

I understand that neither the completion of this application nor any other part of my consideration for employment establishes any obligation for KBI Biopharma, Inc. to hire me. If I am hired, I understand that either KBI Biopharma, Inc. or I can terminate my employment at any time and for any reason, with or without cause and without prior notice. I understand that no representative of KBI Biopharma, Inc. has the authority to make any assurance to the contrary.

I attest with my signature below that I have given to KBI Biopharma, Inc. true and complete information on this application. No requested information has been concealed. I authorize KBI Biopharma, Inc. to contact references provided for employment reference checks. If any information I have provided is untrue, or if I have concealed material information, I understand that this will constitute cause for the denial of employment or immediate dismissal.

 

Job Summary
Company
Start Date
As soon as possible
Employment Term and Type
Regular, Full Time
Required Experience
Open
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