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Cleaning/Maintenance Associate

In Florida / United States

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Cleaning/Maintenance Associate   

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JOB TITLE:
Cleaning/Maintenance Associate
JOB TYPE:

JOB SKILLS:
JOB LOCATION:
US - Alachua Florida / United States

JOB DESCRIPTION :
Description

Pay Rate: XXX

2nd Shift

When you re part of the team at Client Scientific, you ll do important work, like helping customers in finding cures for cancer, protecting the environment, or making sure our food is safe. Your work will have real-world impact, and you ll be supported in achieving your career goals.

Location/Division Specific Information

The Manufacturing Associate is member of the GMP Manufacturing department in Alachua, Florida whose mission is to deliver a consistent and reliable supply of quality released viral vector drug substance and/or drug product that meets regulatory and internal Quality and Safety standards.

How will you make an impact?

During 2nd shift, The Incumbent prepares disinfectants, autoclaves cleaning supplies, cleans/mops production rooms and associated support areas/corridors, disposal of biohazard waste, stocking of gowning materials, stocking locker room supplies, and removal of regular trash from the warehouse areas and locker rooms. The incumbent must also maintain equipment logs and document equipment usage, and document all other assigned cleaning activities as required by written procedures.

The Cleaning Associate is expected to keep the GMP cleanroom in a constant state of inspection readiness and perform routine tasks such as cleaning, decontamination, waste management, equipment maintenance, materials movement and other duties as assigned to assure the cleanroom and manufacturing systems are clean and inspection-ready at-all-times. The Cleaning Associate will adhere to all Safety and Quality standards of the organization contribute to continuous improvement in the areas of Safety, Quality, and Delivery.

What will you do?

  • Perform cGMP manufacturing activities according to standard operating procedures (SOPs) in accordance with assigned daily tasks and production schedule
  • Meticulously maintain facility records and process/system records as required throughout the manufacturing process according to GDP standards
  • Through strict adherence to manufacturing controls, ensure finished drug substance/drug product and all intermediates comply with applicable regulatory requirements (e.g. FDA, EMA), cGMPs, QA/QC and safety standards
  • Ability to learn biopharmaceutical manufacturing processes including but not limited to: cleaning, stocking, disinfectant prep, decontamination, waste management, equipment maintenance, materials movement, staging, etc.
  • Adheres to the production schedule ensuring on-time delivery and efficient production logistics
  • Other activities include keeping the GMP manufacturing facility in a state of inspection readiness, using performance tools (Human Performance), and routine housekeeping activities
  • Other duties as assigned

    How will you get here?

    Required:

  • High School Diploma

    Preferred:

  • Associate Degree in Life Sciences, Engineering, or Biotechnology or certificate program and one to three years industry related experience

    Experience:

  • Manufacturing experience preferred
  • Cleanroom experience preferred

    Knowledge, Skills, Abilities

  • Strong interpersonal and communications skills; written and oral
  • Solid understanding of applicable regulatory requirements
  • Strong working knowledge of Microsoft Office
  • Ability to deliver high quality documentation paying attention to detail
  • The employee must frequently lift and/or move up to 25 pounds and occasionally lift and/or move up to 50 pounds

    Work Hours: Monday through Friday, 3 pm to 11 PM on a FLEX schedule. Overtime, weekend and holidays required to meet project timelines as necessary.

  • At Client Scientific, each one of our 70,000 extraordinary minds has a unique story to tell. Join us and contribute to our singular mission enabling our customers to make the world healthier, cleaner, and safer.

    Skill/Experience/Education
    Cleaning Associate I, Manufacturing
    Contingent Hourly (CWHR)-TEM.CWHR.A00
    Special Needs

    Position Details

    May 09, 2021
    S16119758157783273
    Florida / United States
    US - Alachua
    A job sourcing event
    In Dallas Fort Worth
    Aug 19, 2017 9am-6pm
    All job seekers welcome!

    Cleaning/Maintenance Associate    Apply

    Click on the below icons to share this job to Linkedin, Twitter!

    Description

    Pay Rate: XXX

    2nd Shift

    When you re part of the team at Client Scientific, you ll do important work, like helping customers in finding cures for cancer, protecting the environment, or making sure our food is safe. Your work will have real-world impact, and you ll be supported in achieving your career goals.

    Location/Division Specific Information

    The Manufacturing Associate is member of the GMP Manufacturing department in Alachua, Florida whose mission is to deliver a consistent and reliable supply of quality released viral vector drug substance and/or drug product that meets regulatory and internal Quality and Safety standards.

    How will you make an impact?

    During 2nd shift, The Incumbent prepares disinfectants, autoclaves cleaning supplies, cleans/mops production rooms and associated support areas/corridors, disposal of biohazard waste, stocking of gowning materials, stocking locker room supplies, and removal of regular trash from the warehouse areas and locker rooms. The incumbent must also maintain equipment logs and document equipment usage, and document all other assigned cleaning activities as required by written procedures.

    The Cleaning Associate is expected to keep the GMP cleanroom in a constant state of inspection readiness and perform routine tasks such as cleaning, decontamination, waste management, equipment maintenance, materials movement and other duties as assigned to assure the cleanroom and manufacturing systems are clean and inspection-ready at-all-times. The Cleaning Associate will adhere to all Safety and Quality standards of the organization contribute to continuous improvement in the areas of Safety, Quality, and Delivery.

    What will you do?

  • Perform cGMP manufacturing activities according to standard operating procedures (SOPs) in accordance with assigned daily tasks and production schedule
  • Meticulously maintain facility records and process/system records as required throughout the manufacturing process according to GDP standards
  • Through strict adherence to manufacturing controls, ensure finished drug substance/drug product and all intermediates comply with applicable regulatory requirements (e.g. FDA, EMA), cGMPs, QA/QC and safety standards
  • Ability to learn biopharmaceutical manufacturing processes including but not limited to: cleaning, stocking, disinfectant prep, decontamination, waste management, equipment maintenance, materials movement, staging, etc.
  • Adheres to the production schedule ensuring on-time delivery and efficient production logistics
  • Other activities include keeping the GMP manufacturing facility in a state of inspection readiness, using performance tools (Human Performance), and routine housekeeping activities
  • Other duties as assigned

    How will you get here?

    Required:

  • High School Diploma

    Preferred:

  • Associate Degree in Life Sciences, Engineering, or Biotechnology or certificate program and one to three years industry related experience

    Experience:

  • Manufacturing experience preferred
  • Cleanroom experience preferred

    Knowledge, Skills, Abilities

  • Strong interpersonal and communications skills; written and oral
  • Solid understanding of applicable regulatory requirements
  • Strong working knowledge of Microsoft Office
  • Ability to deliver high quality documentation paying attention to detail
  • The employee must frequently lift and/or move up to 25 pounds and occasionally lift and/or move up to 50 pounds

    Work Hours: Monday through Friday, 3 pm to 11 PM on a FLEX schedule. Overtime, weekend and holidays required to meet project timelines as necessary.

  • At Client Scientific, each one of our 70,000 extraordinary minds has a unique story to tell. Join us and contribute to our singular mission enabling our customers to make the world healthier, cleaner, and safer.

    Skill/Experience/Education
    Cleaning Associate I, Manufacturing
    Contingent Hourly (CWHR)-TEM.CWHR.A00
    Special Needs