Suite Sanitation Manufacturing - Support Services Associate I

Minaris Advanced TherapiesPhiladelphia, PA
Onsite

About The Position

Be part of something bigger at Minaris Advanced Therapies—where every role contributes to creating hope for patients around the world. As a global leader in cell and gene therapy development, manufacturing, and testing, we turn breakthrough science into real-world treatments that change lives. Our team of over 1,000 experts across North America, Europe, and Asia has helped bring transformative therapies to market. At Minaris, you’ll join a purpose-driven community focused on innovation, collaboration, and patient impact. Whether you’re in the lab, in the cleanroom, or behind the scenes, your work will directly support life-saving therapies and make a lasting difference. If you're passionate about advancing cutting-edge science and believe in the potential of cell and gene therapies, we invite you to help shape the future of medicine—one patient at a time.

Requirements

  • Must be able to wear appropriate clean room attire (i.e. surgical masks) and all Personal Protective Equipment (PPE)
  • Possesses basic technical knowledge and background
  • Understands aseptic technique concepts/proper cleanroom behavior
  • Possess basic computer skills and able to efficiently use basic Microsoft applications
  • Thorough understanding of regulatory requirements for cGMP manufacturing facility, especially as they apply to cleaning practices/sterility assurance.
  • Ability to accurately and reproducibly perform arithmetic calculations including fractions, decimals and percentages and basic algebraic and geometric calculations
  • Works in production environment with exposure to latex and bleach. Potential exposure to noise and equipment hazards (i.e. vacuum pumps, pressurized vessels), dangerous materials (i.e. chemicals, solvents, pathogens), freezer burns, allergens and strong odors.
  • Based on work assignments, it may be recommended to have medical testing in accordance with the company’s Occupational Health Program.
  • Proficient in Oral & Written communication skills
  • Need to be able to read, write and understand English
  • Proficient in Microsoft (Excel, Word, Outlook)
  • High School diploma or equivalent
  • 1-2 years of relevant or equivalent experience
  • Ensure compliance with all FDA and Worldwide Quality & Compliance regulations in all aspects of your work.
  • Adhere to established procedures and protocols, prioritize continuous training and skill development, and uphold the highest standards of data integrity to ensure accuracy, compliance, and operational excellence.
  • Must be able to work in Lab Setting with Biohazards/Various Chemicals
  • Must be able to work in an office environment with minimal noise conditions
  • Must be able to wear appropriate PPE
  • Must be able to work in clean room environment
  • Must be able to work in various noise levels
  • Ability to stand/sit/walk for long periods of time
  • Ability to lift, push, pull 40 lbs. routinely, often/occasionally
  • Ability to crouch, bend, twist and reach
  • Clarity of Vision
  • Ability to identify and distinguish colors
  • Must be able to perform activities with repetitive motions
  • Inside/outside working conditions
  • Ability to work in variable temperatures high to freezing
  • Ability to climb Ladders / Stairs / Scaffolding

Nice To Haves

  • May be required to work holidays and weekends
  • May be required to work overtime
  • May be required to work outside of normal business hours
  • Thorough understanding of Good Laboratory Practices and Good Manufacturing Practices

Responsibilities

  • Perform cleaning methods, such as wiping techniques of equipment, wall and ceiling and floor mopping techniques.
  • Responsible for the operation, maintenance and cleaning of equipment
  • Responsible for the cleaning/sanitization solution and material preparation
  • Responsible for receiving and organizing gowning and cleaning materials
  • Identifies and communicates material discrepancies
  • Follows compliance and regulatory requirements and current Good Manufacturing Practices (cGMPs)
  • Follows and executes Standard Operating Procedures (SOPs)
  • May participate in the training activities of others on SOPs, equipment, all unit operations and non-manufacturing SOPs
  • May participate in the training activities of others on basic operations such as cleaning/sanitization of cleanrooms, cleaning and maintenance of equipment, solution and material preparation
  • Participates with technical documents such as non-conforming events and deviations
  • Suggests continuous improvement ideas
  • Follow Proper cleaning/disinfecting schedules
  • Assist Supervision with internal pre-audits walkthroughs, CGMP housekeeping and general organization and upkeep of manufacturing spaces
  • Contributes to the overall operations and to the achievement of departmental goals
  • Perform job specific tasks in compliance with applicable Regulations, International Standards, and Minaris Advanced Therapies Policies and Standard Operating Procedures.
  • Other duties as assigned
  • May be required to assist in other departments

Benefits

  • medical insurance
  • vision insurance
  • dental insurance
  • 401(k)
  • paid time off
  • tuition assistance
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