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Thermo Pac Jobs (NOW HIRING)

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Thermo Pac information

What is a Thermo Pac?

A Thermo Pac job typically involves working in food packaging and production, handling tasks such as operating machinery, monitoring product quality, and ensuring packaging meets safety standards. Employees may work in a fast-paced environment with strict hygiene and safety protocols. Responsibilities can vary by role, but common positions include machine operators, packers, and quality control inspectors.

What are the main responsibilities of a Thermo Pac operator in a typical workday?

As a Thermo Pac operator, your main responsibilities include setting up, monitoring, and maintaining thermoforming and packaging equipment to ensure efficient and safe food packaging operations. You will frequently inspect finished products for quality, troubleshoot machinery when issues arise, and complete necessary production logs or reports. Collaboration with quality control staff and maintenance teams is common to ensure consistent product standards and smooth workflow. Working in this position, you can expect a fast-paced environment with regular standing, machine operation, and adherence to strict safety and hygiene guidelines. Over time, experienced operators may advance into supervisory or maintenance roles within the production facility.

What are the key skills and qualifications needed to thrive in the Thermo Pac position, and why are they important?

To thrive in a Thermo Pac role—typically referring to an operator or technician within food packaging and processing—you need mechanical aptitude, attention to safety protocols, and a high school diploma or equivalent. Familiarity with thermoforming machinery, packaging systems, and basic quality control procedures is important, and some employers may require certifications in equipment operation or food safety. Strong teamwork, problem-solving skills, and effective communication will help you excel in fast-paced production environments. These abilities ensure safe, efficient operation, minimize errors, and promote a collaborative workplace focused on delivering high-quality packaged goods.

More about Thermo Pac jobs
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Infographic showing various Thermo Pac job openings in the United States as of August 2026, with employment types broken down into 70% Full Time, 20% Part Time, and 10% Nights. Highlights an 100% In-person job distribution.

Clinical Research Coordinator I

Thermo Fisher Scientific

Richfield, MN • On-site

$25 - $28/hr

Full-time

Medical, Dental, Vision, Life, Retirement, PTO

This job post has expired today. Applications are no longer accepted.


Thermo Fisher Scientific rating

7.7

Company rating: 7.7 out of 10

Based on 424 frontline employees who took The Breakroom Quiz

200th of 538 rated manufacturers


Job description

Work Schedule
Standard (Mon-Fri)
Environmental Conditions
Office
Job Description
Join us as a Clinical Research Coordinator I - Provides administrative and technical support to the Project Team. Supports audit readiness by ensuring files are reviewed according to the schedule detailed in the organization's SOP and department guidance document. Provides administrative support for site activation activities. Aids the development of the critical path for site activation within assigned projects in support of rapid site activations. Represents CRG personnel. May utilize local knowledge, organization systems, external site lists and sponsor directives to develop and review site lists that are suitable for the strategic needs of feasibility activities and to provide local input into the site tiering process. May act as a buddy during onboarding phase and provide training to new staff as needed.
Education and Experience:
• Bachelor's degree or equivalent and relevant formal academic / vocational qualification
• BLS certificate required.
• Previous experience to provide the knowledge, skills, and abilities to perform the job (comparable to 0- 2+ years')
• According to the specific role (Central or Local), coordinates, oversees and completes functions on assigned trial(s) activities as detailed on the task matrix.
• Performs department, Internal, Country and Investigator file reviews as assigned, and documents findings in appropriate system(s).
• Ensures allocated tasks are performed on time, within budget and to a highquality standard. Proactively communicates any risks to project leads.
• Provides system support (i.e., Activate & eTMF) and ensures system databases are always current.
• Performs administrative tasks on assigned trials, including, but not limited to, timely processing of documents sent to Client (e)TMF as assigned, performing (e)TMF reviews, distributing mass mailings and communications as needed, providing documents and reports to internal team members.
• Analyzes and reconciles study metrics and findings reports. Assists with clarification and resolution of findings related to site documentation.
• Assists with coordination, compilation and distribution of Investigator Site File (ISF) and Pharmacy binder materials and non-clinical study supplies to sites.
• Assists with study-specific translation materials and translation QC upon request.
• Maintains knowledge of and understands SOPs, client SOPs/directives, and current regulatory guidelines as applicable to services provided.
• Where applicable, conducts on-site feasibility visits (Asia Pac only).
• May support scheduling of client and/or internal meetings.
• May review and track of local regulatory documents.
• May provide system support (i.e., Activate & eTMF). May support RBM activities.
• May support the maintenance of study specific documentation and systems, including, but not limited to, study team lists, tracking of project specific training requirements, system access management and tracking of project level activity plans in appropriate system(s).
• Transmits documents to client and centralized IRB/IEC.
• Maintains vendor trackers.
• Supports start-up team in Regulatory submissions.
• Works directly with sites to obtain documents related to site selection.
Compensation and Benefits
The hourly pay range estimated for this position based in Minnesota is $25.00-$28.00.
This position may also be eligible to receive a variable annual bonus based on company, team, and/or individual performance results in accordance with company policy. We offer a comprehensive Total Rewards package that our U.S. colleagues and their families can count on, which includes:
  • A choice of national medical and dental plans, and a national vision plan, including health incentive programs
  • Employee assistance and family support programs, including commuter benefits and tuition reimbursement
  • At least 120 hours paid time off (PTO), 10 paid holidays annually, paid parental leave (3 weeks for bonding and 8 weeks for caregiver leave), accident and life insurance, and short- and long-term disability in accordance with company policy
  • Retirement and savings programs, such as our competitive 401(k) U.S. retirement savings plan
  • Employees' Stock Purchase Plan (ESPP) offers eligible colleagues the opportunity to purchase company stock at a discount

For more information on our benefits, please visit: https://jobs.thermofisher.com/global/en/total-rewards

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