In-Process Support Associate

Posted 4 Days Ago
Be an Early Applicant
National, MD
Entry level
Biotech
The Role
The In-Process Support Associate conducts cGMP in-process analytical support through bio-analytical testing including HPLC and UV-Vis techniques. Responsibilities involve detailed observations, data analysis, documentation upkeep, and adherence to safety regulations. The role requires flexibility for testing needs during non-standard hours.
Summary Generated by Built In

Position Summary:
KBI Biopharma, Inc. is a contract services organization committed to reducing process development time, decreasing production cost and increasing speed of development for biopharmaceuticals. We are seeking an In-Process Support Associate with strong protein chemistry background to perform cGMP in-process analytical support. These services include in-process and release testing for drug substances manufactured internally.

Position Responsibilities:

  • Performs testing on in-process or drug substance/drug product using bio-analytical techniques such as (but not limited to) HPLC, UV-Vis and simple compendial testing. Regularly exercises technical discretion in the execution and interpretation of experiments that contribute to project goals

  • Makes detailed observations and carries out elementary data analysis

  • Understand experiments, conducts troubleshooting analysis, and maintains knowledge of instrumentation

  • Documentation (i.e. Notebook and Worksheet) upkeep and writing skills

  • Maintains familiarity with current scientific literature; maintains professional expertise through familiarity with scientific literature

  • Assures proper labeling, handling, and storage of all chemicals used in the area, assures proper labeling and disposition of hazardous waste in satellite area; adheres to all safety requirements and follows safety procedures, and attends all required safety and health training, including handling hazardous waste

  • Able to react to change productively and handle other essential tasks as assigned

Position Requirements:

  • BS in scientific discipline or equivalent with a minimum of 0-2 years’ experience in QC analysis of proteins, antibodies, peptides, or vaccines.

  • Excellent verbal and written communication skills.

  • Experience working in a cGMP environment preferred.

  • Flexible work schedule to accommodate manufacturing testing needs as STAT testing may be required during evening and/or weekend hours.

Salary: $18.80-$25.85/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, Sabbatical program, 401K matching with 100% vesting in 60 days and employee recognition programs. 

KBI Biopharma is committed to providing a safe and healthy workplace. Any employee entering a KBI site located in the US must inform KBI Biopharma of their vaccination status and must submit their vaccination status. All vaccinated employees are required to provide proof of their COVID-19 vaccination, with a COVID-19 vaccination which has been granted FDA approval or Emergency Use Authorization.

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.

Top Skills

Hplc
Uv-Vis
The Company
Boulder , CO
1,282 Employees
On-site Workplace
Year Founded: 1996

What We Do

KBI Biopharma is an award-winning biopharmaceutical contract services organization providing fully-integrated, accelerated drug development and biomanufacturing services to pharmaceutical and biotechnology companies globally.

With each of our 500+ client partners, we have worked closely to personalize and rapidly accelerate their drug development programs. Built upon a foundation of world-class analytical capabilities, we deliver efficient process development and clinical and commercial cGMP manufacturing services for mammalian, microbial, and cell therapy programs.

KBI is proud to be a JSR Life Sciences Company.

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