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Temporary Fda Regulatory Jobs (NOW HIRING)

TekWissen LLC

Packaging Operator I

Tampa, FL · On-site

$15 - $20/hr

Temporary Assignment Work Type: Onsite Shift: 07:00 AM to 03:30 PM Summary * Operate and tend ... Working knowledge of cGMP and FDA regulations * Strong attention to detail with accurate and timely ...

TekWissen LLC

Packaging Operator I

Tampa, FL · On-site

$20 - $24/hr

Temporary Assignment Work Type: Onsite Shift: 3rd Shift Summary * Operate and tend packaging ... Working knowledge of cGMP and FDA regulations * Strong attention to detail with accurate and timely ...

KVK Tech

Be Seen First

Lead Packaging Mechanic (3:30pm-12:00am)

Newtown, PA · On-site

$42 - $48/hr

... mechanics, operators, or temporary personnel on safe operation, equipment setup, and ... Knowledge of cGMP, GDP, and FDA regulatory expectations for pharmaceutical packaging operations.

University of Miami

Regulatory Analyst 2

Miami, FL · On-site

If you are a current Staff, Faculty or Temporary employee at the University of Miami, please click ... FDA, NIH, and other applicable regulations. * Adheres to University and unit-level policies and ...

The University of Miami

Regulatory Analyst 2

Miami, FL · On-site

If you are a current Staff, Faculty or Temporary employee at the University of Miami, please click ... FDA, NIH, and other applicable regulations. * Adheres to University and unit-level policies and ...

AtriCure

Regulatory Affairs Specialist

Mason, OH · On-site

AtriCure's Isolator ® Synergy™ Ablation System is the first medical device to receive FDA ... AtriCure's cryoICE cryoSPHERE ® probe is cleared for temporary ablation of peripheral nerves to ...

Uw

Research Coordinator 3 (Temporary)

Seattle, WA · On-site

$87K/yr

... temporary Research Coordinator 3 to join their team. About this Opportunity Reporting to the ... Familiarity with FDA regulations. * Certification in Good Clinical Practices. * Appropriate ...

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How much do temporary fda regulatory jobs pay per hour?

As of Aug 19, 2026, the average hourly pay for temporary fda regulatory in the United States is $39.57, according to ZipRecruiter salary data. Most workers in this role earn between $31.73 and $46.88 per hour, depending on experience, location, and employer.

What is a temporary FDA regulatory?

Temporary FDA Regulatory jobs involve short-term roles focused on ensuring that products and processes comply with the regulations set by the U.S. Food and Drug Administration (FDA). These positions may include responsibilities like preparing regulatory submissions, assisting with audits, monitoring compliance, and supporting the development of documentation for FDA approval. Temporary roles are often filled to address project-based needs, help with workload spikes, or provide specialized expertise for a limited time. They are common in industries such as pharmaceuticals, medical devices, and food manufacturing where regulatory oversight is critical. Such positions require knowledge of current FDA regulations and strong attention to detail.

What skills and qualifications are needed for a temporary FDA regulatory?

To thrive as a Temporary FDA Regulatory Specialist, you need a solid understanding of FDA regulations, compliance standards, and regulatory submission processes, often supported by a degree in life sciences or a related field. Familiarity with regulatory submission tools (such as eCTD software), document management systems, and potentially certifications like RAC (Regulatory Affairs Certification) is valuable. Attention to detail, strong organizational skills, and clear communication are crucial soft skills for managing documentation and cross-functional collaboration. These competencies ensure timely and accurate regulatory submissions, minimizing compliance risks and supporting successful product approvals.

What are common challenges faced by temporary FDA regulatory professionals?

Professionals in temporary FDA regulatory positions often encounter the challenge of quickly adapting to new organizational processes and understanding the specific regulatory landscape of the company. Since these roles are short-term, there is typically a steep learning curve to become proficient with internal documentation systems, ongoing submissions, and compliance protocols. Additionally, effective communication and collaboration with cross-functional teams, such as R&D, quality assurance, and legal, are essential to ensure timely and accurate regulatory filings. Temporary staff must also stay up-to-date with evolving FDA regulations to minimize compliance risks for the organization.

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Temporary Fda Regulatory jobs near you

Packaging Operator I

TekWissen LLC

Tampa, FL • On-site

$15 - $20/hr

Temporary

Re-posted 15 days ago

Job description

Overview:  
  
TekWissen is a global workforce management provider headquartered in Ann Arbor, Michigan that offers strategic talent solutions to our clients world-wide.  Our client is a leading biotechnology company that combines technological insight with world-class manufacturing, scientific expertise, and process excellence and helps their customers to deliver new and innovative medicines that help treat a wide range of diseases. Our client specializes in pharmaceutical ingredients, Bioscience, Biopharmaceuticals, Custom manufacturing, Biotechnology, Life science ingredients, Nutrition, Microbial Control, Agriculture, Materials Science, Personal Care, and cell and gene therapy.  
  
Job Title:     Packaging Operator I
Location:     Tampa, FL, 33634 
Duration:     12 Months    
Job Type:    Temporary Assignment 
Work Type: Onsite
 Shift:           07:00 AM to 03:30 PM
 
Summary
  • Operate and tend packaging equipment performing functions such as filling, marking, labelling, tying, packing, or wrapping containers.
  • Execute packaging and labelling activities in accordance with Batch Record requirements and cGMP guidelines, ensuring accurate, timely, and compliant documentation.
  • Provide operational support to Manufacturing, Quality Assurance, Warehouse, and Facilities while adhering to company and FDA regulatory requirements.
  • The role also includes responsibility for cleaning and sanitization of primary and secondary packaging rooms and equipment.
Responsibilities
  • Follow batch record instructions to execute manual processes for primary and secondary packaging activities.
  • Assist in the operation and setup of automated packaging equipment for designated packaging operations.
  • Support the reconciliation and movement (chain of custody) of materials between packaging areas and the warehouse.
  • Perform cleaning and sanitization of primary and secondary packaging rooms and packaging equipment in accordance with departmental procedures.
  • Report observations or potential issues that may result in deviations or investigations to QA, Team Lead, Equipment Specialist, CPS Project Coordinator, or Manager.
  • Support Equipment Specialists with the execution of qualification protocols for new equipment as assigned.
  • Maintain current training on SOPs, GMP documentation, and logbook entries relevant to job responsibilities.
  • Attend required meetings and discussions to support production schedules and project execution.
  • Participate in applicable safety processes and meetings.
  • Maintain professional, positive, and confidential relationships and comply with all state and federal regulatory requirements.
  • Promptly report safety and sustainability concerns and stop work when necessary to ensure safety.
  • Perform other duties as assigned.
Required Qualifications
  • 1–3 years of experience operating or tending packaging equipment in a manufacturing environment
  • Experience with primary and secondary packaging operations
  • Familiarity with automated packaging equipment
  • Experience working in regulated manufacturing environments (pharmaceutical, biotech, or medical device)
  • Knowledge of equipment qualification activities
  • Experience supporting cross-functional teams including QA, Warehouse, and Facilities
  • Ability to follow batch records and execute packaging and labelling processes accurately
  • Working knowledge of cGMP and FDA regulations
  • Strong attention to detail with accurate and timely documentation practices
  • Ability to support cleaning and sanitization activities in controlled environments
  • Basic mechanical aptitude to assist with equipment setup and operation
  • Ability to communicate observations and issues clearly to cross-functional teams
  • Commitment to workplace safety and compliance standards
TekWissen® Group is an equal opportunity employer supporting workforce diversity.    

TekWissen is an emerging global human capital, recruitment and IT services organization. Operating since 2009, we draw upon more than a decade of staffing experience to deliver critical talent acquisition solutions and IT engagements for our clients. We’re founded on a culture that is passionate about delivering tailored solutions, that create lasting partnerships.

Our global footprint covers six countries: United States, Canada, Australia, India, United Kingdom and the Philippines. This allows us to work in close partnership with organizations and manage everything from global talent needs with demanding resourcing strategies, to single sites with lower recruitment volumes.

TekWissen® is an equal opportunity employer supporting workplace diversity. 

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About TekWissen

Sourced by ZipRecruiter

TekWissen is an emerging global human capital, recruitment and IT services organization. Operating since 2009, we draw upon more than a decade of staffing experience to deliver critical talent acquisition solutions and IT engagements for our clients. We’re founded on a culture that is passionate about delivering tailored solutions, that create lasting partnerships.

Industry

Recruiting and staffing services

Company size

501 - 1,000 Employees

Headquarters location

Ann Arbor, MI, US

Year founded

2009

Social media

Twitter

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