• Technician

    Actalent (Minneapolis, MN)


    Job Title: TechnicianJob Description

     

    As a Technician, you will be responsible for writing, reviewing, and approving qualification and validation protocols for new or transferred equipment and packaging designs. This role involves creating Installation Qualification (IQ), Operational Qualification (OQ), and Performance Qualification (PQ) protocols, as well as drafting Standard Operating Procedures (SOPs), verification protocols, and technical reports.

    Responsibilities

    + Write, review, and approve qualification and validation protocols for equipment and packaging designs.

    + Support CI Engineering in executing equipment and packaging qualification and validation protocols.

    + Collaborate with engineering to create test plans and timelines for manufacturing equipment and packaging designs.

    + Evaluate equipment or packaging for validation requirements.

    + Perform operational testing of semi-automated manufacturing equipment and create operation and debugging procedures.

    + Execute testing for new packaging, including internal and external testing.

    + Communicate clearly and effectively with team members.

    + Understand and follow lab protocols, SOPs, and ensure regulatory compliance.

    + Perform additional duties as assigned.

    Essential Skills

    + 1-2 years of technical experience in a life sciences or related field.

    + Experience with manufacturing and automation equipment.

    + Proficiency in writing and executing qualification and validation protocols.

    + Good communication skills in verbal and written English.

    + Strong computer skills, including Word, Excel, PowerPoint, and Smartsheet.

    + Ability to handle heavy items (5-50lbs).

    + Strong organizational skills and attention to detail.

    Additional Skills & Qualifications

    + Experience with small to medium range filling, capping, and labeling equipment.

    + Experience in an ISO or GMP biotech environment.

    + Experience writing SOPs for equipment, IQ, OQ, PQ.

    + Associates Degree.

    + Experience in data entry, pharmaceutical, and medical device fields.

    + Packaging experience and equipment validation experience.

    + Experience working in a lab or pharmaceutical setting.

     

    Work Environment

     

    Work will be conducted in a lab and clean room environment, involving both lab and equipment work.

    Pay and Benefits

    The pay range for this position is $28.00 - $33.00/hr.

     

    Eligibility requirements apply to some benefits and may depend on your job classification and length of employment. Benefits are subject to change and may be subject to specific elections, plan, or program terms. If eligible, the benefits available for this temporary role may include the following:

     

    • Medical, dental & vision • Critical Illness, Accident, and Hospital • 401(k) Retirement Plan – Pre-tax and Roth post-tax contributions available • Life Insurance (Voluntary Life & AD&D for the employee and dependents) • Short and long-term disability • Health Spending Account (HSA) • Transportation benefits • Employee Assistance Program • Time Off/Leave (PTO, Vacation or Sick Leave)

     

    Workplace Type

     

    This is a fully onsite position in Minneapolis,MN.

     

    Application Deadline

     

    This position is anticipated to close on Jul 25, 2025.

    About Actalent

    Actalent is a global leader in engineering and sciences services and talent solutions. We help visionary companies advance their engineering and science initiatives through access to specialized experts who drive scale, innovation and speed to market. With a network of almost 30,000 consultants and more than 4,500 clients across the U.S., Canada, Asia and Europe, Actalent serves many of the Fortune 500.

     

    The company is an equal opportunity employer and will consider all applications without regard to race, sex, age, color, religion, national origin, veteran status, disability, sexual orientation, gender identity, genetic information or any characteristic protected by law.

     

    If you would like to request a reasonable accommodation, such as the modification or adjustment of the job application process or interviewing due to a disability, please email [email protected] (%[email protected]) for other accommodation options.