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Fda Regulatory Entrylevel Jobs in California (NOW HIRING)

The Regulatory Affairs Associate is an entry-level position for an individual committed to ... Support product registrations and regulatory submissions to FDA and other regulatory bodies ...

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The Regulatory Affairs Associate is an entry-level position for an individual committed to ... Support product registrations and regulatory submissions to FDA and other regulatory bodies ...

Strong emphasis on documentation according to FDA regulations. * Adhere to departmental corporate ... Trains entry level personnel. * Performs more complex and advanced job tasks. * Assist management ...

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Machine Operator

Camarillo, CA · On-site

$17.25 - $20.75/hr

Ability to speak and read English to follow safety instructions, SOPs, GMPs, and FDA regulations ... A full onsite gym encourages a healthy lifestyle, and many leaders have advanced from entry-level ...

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Operator I

Del Rey, CA · On-site

$22/hr

Problem-Solving Skills: * Entry-level assemblers should possess basic problem-solving skills to ... and FDA regulations. * May assemble electronic components and modules according to detailed ...

... and regulatory quality standards. Responsibilities: * Inspect and test raw materials, in-process ... Familiarity with relevant standards (ISO, GMP, FDA) depending on industry. (Qualifications ...

... and regulatory quality standards. Responsibilities: * Inspect and test raw materials, in-process ... Familiarity with relevant standards (ISO, GMP, FDA) depending on industry. (Qualifications ...

... and regulatory quality standards. Responsibilities: * Inspect and test raw materials, in-process ... Familiarity with relevant standards (ISO, GMP, FDA) depending on industry. (Qualifications ...

... and regulatory quality standards. Responsibilities: * Inspect and test raw materials, in-process ... Familiarity with relevant standards (ISO, GMP, FDA) depending on industry. (Qualifications ...

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R&D Associate

Cypress, CA · On-site

$27/hr

Ability to understand and implement FDA, USDA and other related regulations * Basic knowledge of ... entry level to executive leadership. Our mission is to connect employers with the right talent--and ...

Pharmacist I

Antioch, CA · On-site

$85 - $104.96/hr

... USP , FDA regulations (such as the DSCSA), California Business and Professions Codes, OSHA ... Position is entry level and requires 0-3 years' experience as a registered pharmacist required.

... regulatory requirements such as FDA, CAP, CLIA, as well as internal policies and processes Identify the optimum combination of applications that meet the requirements of disparate laboratory and ...

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Regulatory Affairs Associate

PrideStaff

Tustin, CA • On-site

$32 - $36/hr

Full-time

Medical, Dental, Vision, Retirement

Posted 3 days ago

New


Job description

Regulatory Affairs Associate for a biotechnology company located in Tustin. 
Temporary to Hire opportunity. Paying $32-36/hr, depending on qualifications. Hours are 9:00 AM - 5:00 PM, Monday-Friday. Company will complete a background check and drug screen prior to start. 
Summary:

Looking for a motivated individual to join our Regulatory Affairs team! In this role, you will play a vital part in supporting regulatory activities and maintaining compliance with applicable requirements, utilizing your skills and expertise in regulatory documentation, coordination, and compliance support. Your contributions will help ensure high-quality, compliant regulatory processes that support the company.

The Regulatory Affairs Associate is an entry-level position for an individual committed to developing a career in Regulatory Affairs. The role supports Regulatory Affairs activities primarily for the company and may also support affiliated companies as business needs require, with training and guidance from experienced Regulatory Affairs personnel.

Essential Duties and Responsibilities:

  • Support company registrations and device listings in domestic (U.S.) and international markets.
  • Support preparation and maintenance of IVDD/IVDR technical documentation and registrations.
  • Support product registrations and regulatory submissions to FDA and other regulatory bodies including 510(k) submissions as applicable.
  • Research applicable regulations, standards, and guidance documents and summarize findings for review.
  • Assist with reviewing and writing SOPs and other Regulatory Affairs policies as necessary.
  • Coordinate with cross functional teams regarding product changes and regulatory notification and/or approval requirements.
  • Perform initial reviews of marketing materials, labels, and public communications for regulatory compliance under guidance.
  • Assist with evaluating product compliance with applicable regulations and project requirements.
  • Assist with and participate in notified body audits, ISO registrar audits, government inspections, customer audits, and other audits or regulatory activities as needed.
  • Support Regulatory Affairs projects across the company and affiliated companies and perform other related duties as business needs require.

Education and Experience:

  • Bachelor’s degree in a science or related discipline preferred. Entry-level candidates and recent graduates are encouraged to apply; prior Regulatory Affairs experience is not required.
  • Demonstrated interest in developing a long-term career in Regulatory Affairs.
  • Positive, collaborative, and professional attitude with a strong willingness to learn and contribute to the team.
  • Demonstrates initiative, ownership, and willingness to take on new responsibilities and unfamiliar assignments as learning opportunities.
  • Flexible and adaptable, with the ability to research and work through regulatory questions that may require interpretation, judgment, and guidance.
  • Highly organized and efficient, with strong attention to detail, time management, and ability to prioritize multiple tasks.
  • Ability to work independently when appropriate, use MS Office to organize information for reports and presentations, and handle confidential information with professional integrity.

PrideStaff logo

About PrideStaff

Sourced by ZipRecruiter

Accountability of local ownership along with the resources and expertise that the $200m national organization of PrideStaff backing us has. Therese is involved in all day-to-day operations. She leads a dynamic team of recruiters who together are focused on ensuring both clients and candidates have an exceptional experience. When you call the office, it is not unusual that Therese will answer the phone. Along with her team, she conducts interviews and helps with the hiring process. Additionally, PrideStaff’s 80+ other locations across the United States gives us resources not available to most other local staffing firms. It’s not what we say about ourselves that matters…it’s what has been said in our over 3,800 client testimonials that we’ve received over the years that matters.

Industry

Recruiting and staffing services

Company size

501 - 1,000 Employees

Headquarters location

Fresno, CA, US