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Regulatory Affairs Associate Two Jobs (NOW HIRING)

Obagi Medical

Regulatory Affairs Associate

Long Beach, CA · On-site

$35 - $40/hr

Obagi is seeking a reliable and meticulous Regulatory Affairs Associate to help the Regulatory team ensure global compliance across its collection of skincare products. This individual will help ...

AstraZeneca

Regulatory Affairs Associate

Gaithersburg, MD · On-site

$85K - $127K/yr

The Regulatory Affairs Associate (RAA) assists other members of Regulatory Affairs Management (RAM) in obtaining and maintaining licenses and applications in accordance with agreed regulatory ...

Abbott

$40 - $46/hr

Regulatory Affairs Associate Location: Sylmar, CA Duration: 7 Months 100% Onsite Summary: Responsible for filing necessary regulatory applications and supporting interactions with U.S. and ...

Astrazeneca

Regulatory Affairs Associate

Santa Clara, CA · On-site

$85K - $127K/yr

The Regulatory Affairs Associate (RAA) assists other members of Regulatory Affairs Management (RAM) in obtaining and maintaining licenses and applications in accordance with agreed regulatory ...

Astrazeneca

Regulatory Affairs Associate

Gaithersburg, MD · On-site

$85K - $127K/yr

The Regulatory Affairs Associate (RAA) assists other members of Regulatory Affairs Management (RAM) in obtaining and maintaining licenses and applications in accordance with agreed regulatory ...

AstraZeneca

Regulatory Affairs Associate

Cambridge, MA · On-site

$85K - $127K/yr

The Regulatory Affairs Associate (RAA) assists other members of Regulatory Affairs Management (RAM) in obtaining and maintaining licenses and applications in accordance with agreed regulatory ...

AstraZeneca

Regulatory Affairs Associate

Gaithersburg, MD · On-site

$85K - $127K/yr

The Regulatory Affairs Associate (RAA) assists other members of Regulatory Affairs Management (RAM) in obtaining and maintaining licenses and applications in accordance with agreed regulatory ...

Astrazeneca

Regulatory Affairs Associate

Cambridge, MA · On-site

$85K - $127K/yr

The Regulatory Affairs Associate (RAA) assists other members of Regulatory Affairs Management (RAM) in obtaining and maintaining licenses and applications in accordance with agreed regulatory ...

AstraZeneca

Regulatory Affairs Associate

Gaithersburg, MD · On-site

$85K - $127K/yr

The Regulatory Affairs Associate (RAA) assists other members of Regulatory Affairs Management (RAM) in obtaining and maintaining licenses and applications in accordance with agreed regulatory ...

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All JobsRegulatory Affairs Associate Two Jobs

Regulatory Affairs Associate Two information

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$62

How much do regulatory affairs associate two jobs pay per hour?

As of Aug 6, 2026, the average hourly pay for regulatory affairs associate two 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 the difference between Regulatory Affairs Associate Two vs Regulatory Affairs Associate One?

AspectRegulatory Affairs Associate TwoRegulatory Affairs Associate One
Required CredentialsBachelor's degree, relevant certifications often preferredBachelor's degree, entry-level certifications may suffice
Work EnvironmentMid-level regulatory team, more independent responsibilitiesEntry-level, supervised tasks within regulatory teams
Employer & Industry UsagePharmaceutical, biotech, medical device companiesSimilar industries, often within larger regulatory departments
Common Search & Comparison IntentUnderstanding role progression and responsibilitiesEntry-level position details and requirements

The main difference between Regulatory Affairs Associate Two and Regulatory Affairs Associate One lies in experience and responsibilities. Associate Two typically has more experience, handles more complex tasks independently, and may require relevant certifications. Associate One is an entry-level role focused on foundational regulatory tasks. Both roles are common in the pharmaceutical and biotech industries, with Associate Two representing a more advanced position within the regulatory team.

Is regulatory affairs a stable career?

Regulatory affairs is generally considered a stable career due to consistent demand in industries like pharmaceuticals, medical devices, and biotechnology. Professionals in this field often require specialized knowledge of regulations and may hold certifications, which support long-term employment opportunities.
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Regulatory Affairs Associate Two jobs near you
Infographic showing various Regulatory Affairs Associate Two job openings in the United States as of August 2026, with employment types broken down into 1% As Needed, 69% Full Time, 27% Part Time, 1% Temporary, and 2% Contract. Highlights an 97% Physical, 1% Hybrid, and 2% Remote job distribution, with an average salary of $82,307 per year, or $39.6 per hour.

Regulatory Affairs Associate

Obagi Medical

Long Beach, CA • On-site

$35 - $40/hr

Contractor

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

Job description

Salary range: $35.00 - $40.00/hour
Who We Are:
Obagi Cosmeceuticals is an industry leading dermo-cosmetic brand that provides transformational skin care products, with a 35+ year legacy backed by science and innovation to protect and enhance skin tone and texture. Obagi is widely recognized by US dermatologists and plastic surgeons for its clinical excellence and science-backed approach, remaining a leader in the beauty space and operates as an innovative, global, omni-channel luxury consumer products business with sales distribution to physicians, wholesale partners, retail outlets, Amazon, and direct-to-consumer (DTC) channels. On a mission to create a global, best-in-class multi-brand, multicategory portfolio, Obagi will continue to redefine the future of skincare. We are Obagi. Fearless. Together.
What We Need:
Obagi is seeking a reliable and meticulous Regulatory Affairs Associate to help the Regulatory team ensure global compliance across its collection of skincare products. This individual will help organize, manage, and maintain files across our databases and platforms, along with ensuring that all files adhere to regulatory and compliance requirements across the jurisdictions where our operations extend.
What You'll Do:
  • Reviewing ingredients for regulatory compliance for different markets and product categories.
  • Partner with manufacturers and ingredient suppliers to acquire all necessary documentation to maintain an accurate library of robust products and raw materials.
  • Prepare, compile, and organize all relevant documentation for product registrations and listings.
  • Ensure renewals for state licenses.
  • Maintain business systems, databases, and knowledge sharing systems as appropriate.
  • Coordinate FDA Drug Listing submissions for Rx and OTC products under supervision from Regulatory Leadership
  • Ensure appropriate follow-up correspondence, such as re-submissions, re-certifications, renewals as required.
  • Other duties as assigned by the Supervisor.
What You'll Need:
  • A bachelor's degree from an accredited university is required. A focus in Life Sciences or Chemistry is highly preferred.
  • At least 3-4+ years of relevant experience within regulatory affairs; familiarity with regulatory frameworks across various jurisdictions and a keen ability to accurately interpret and apply them real time.
  • Exceptional organizational and prioritization/time management skills; demonstrated ability to work under pressure to meet deadlines.
  • Comfortable operating in a fast paced, ever-changing environment; someone who thrives in ambiguity and adapts quickly.
  • Proficiency in Microsoft Office and other technologies.
  • An energetic, positive attitude that encourages a team and supports the growth and professional development of others.
Physical Requirements:
These demands document the physical requirements of a specific job. Criteria may include: Lifting, Carrying, Push/Pull, Sitting/Standing (In Place); On Feet, Walking, Bending, Turn/Twist; Kneeling; Squatting; Crawling; Climbing; Reaching (Out)/Reaching (Up), Grasping, Wrist Turning; Pinching; Finger Manipulation, Hearing, Talking, Working with a computer for eight hours, Working in close quarters. Communicating over the telephone for eight hours.
Disclaimer:
The above statements are intended to describe the general nature and level of work being performed by people assigned to this classification. They are not to be construed as an exhaustive list of all responsibilities, duties, and skills required of job requirements, so classified. All employees may be required to perform duties outside of their normal responsibilities, from time to time, as needed.

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