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Biomanufacturing Operator 1

Company: Kelly Services
Location: Davenport
Posted on: April 10, 2021

Job Description:

Biomanufacturing Operator 1Direct HireRelocation ProvidedPay Rate- $20-$30 per hourSigning Bonus $1,000 for dayshift and $2000 for night shiftHealth, dental, vision, 401k with company match25% Shift Differential increase for night shiftShifts:1st Shift - 6:00-4:30 pm2nd shift - 3:30 pm-2:00 am

  • Upstream------------ Monday-Friday 7:00-4:00Tuesday-Friday 3 pm-2am
  • DownstreamMonday-Tuesday (off W, Th)Friday-Sunday (off M)Tuesday-Thursday (off Fr, Sa, Sun)Position Summary--The Biomanufacturing Operator will work daily within the labs performing tasks associated with GMP services. The Biomanufacturing Operator is expected to become familiar with all Company products and to be able to perform most tasks associated with the purification of plasmid DNA.Essential Functions
  • Segregation, line clearance and cleaning of GMP production areas--
  • Plan and submit inventory requisitions--
  • Plan and preparation--of--production events and--process plan memos--
  • Coordinate--production events with buffer preparation operators?--
  • Execute--GMP, dispensing, projects:--filtration, formulation, environmental monitoring, manual and semi-automated dispensing, and media fill and gowning qualification events;--all special considerations associated--
  • May include cross training on any of the items listed below--
  • Upstream tasks--include--transformation,--subculture,--cell banking, shake, flask growth and harvest,--wave growth and harvest,--fermentation,--media fill events,--final formulation, filtration, and--dispersion--
  • Downstream tasks--include--project--set up,--lysis,--anion--exchange--chromatography, and--hydrophobic--interaction--chromatography (void and enrichment),--thiophilic--absorption--chromatography, defiltration, small scale, processing,--and--linearization--
  • Completion of all documentation associated with GMP projects--
  • Coordination and sample submission with Quality Control--
  • Equipment calibration and preventative maintenance--
  • Assist in writing--manufacturing--summary--reports after project completion--
  • Maintain personnel training record--
  • Assist with assembly and segregation of all consumables and equipment resources for GMP production runs--
  • Participate and support--in--the internal audit program--and provide--requested information and respond to findings presented in the audit report--
  • Communicate the status of operations, process issues, safety, and maintenance issues to appropriate area--of--management--
  • Follow all Company SOP's and adhere--to regulatory expectations--
  • Completion and maintenance of GMP Bill of Materials for GMP projects--
  • Perform other duties as assigned
  • All employees are responsible for the general upkeep of work and shared spaces
  • Punctual and regular attendance is required of all employeesQualificationsExperience:
    • Prefer at least 2 years of technical laboratory experience in a regulated industry
    • Recent college graduates welcome to apply
    • GMP and downstream experience a plusEducation
      • High school diploma required
      • Bachelor of Science in life science (biology, chemistry, biotechnology) preferredSkills & Knowledge
        • Excellent written and verbal communication skills--
        • Apply basic math (arithmetic, ratios, proportions, and conversions)--
        • Knowledge of computers and programs (i.e. Microsoft Office and Smartsheet)
        • Organizational skills--
        • Follow-through on methodology, understand that bacteria are living organisms that do not adhere to a scheduleAbilities
          • Ability to work effectively within a team
          • Ability to pipette into small vials efficiently and accurately
          • Ability to shake, move, agitate, etc. glass vials and bottles--
          • Ability to lift and move materials and equipment
          • Ability to follow written--procedures and--both written and verbal directions
          • Ability to accurately keep records and maintain files
          • Ability to self-report mistakes or concerns to the manager----
            Why Kelly--?Kelly Science & Clinical is your connection to premier scientific and clinical companies looking to hire talented people just like you. Every day, we match science professionals with dream jobs that fit their skills and interests-it's the way we think job searching should be. Nearly 100 percent of our science recruiters have a professional background/education in science, so we know a thing or two about the science market and how to get you noticed.About Kelly--At Kelly, we're always thinking about what's next and advising job seekers on new ways of working to reach their full potential. In fact, we're a leading advocate for temporary/nontraditional workstyles, because we believe they allow flexibility and tremendous growth opportunities that enable a better way to work and live. Connecting great people with great companies is what we do best, and our employment opportunities span a wide variety of workstyles, skill levels, and industries around the world. Kelly is an equal opportunity employer committed to employing a diverse workforce, including, but not limited to, minorities, females, individuals with disabilities, protected veterans, sexual orientation, gender identity. Equal Employment Opportunity is The Law.]]

Keywords: Kelly Services, Fargo , Biomanufacturing Operator 1, Other , Davenport, North Dakota

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