Jobs in the United States

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Added 3 mins ago
J
Retail Associate, PT - Nike Lakewood
Lakewood, CO
- $19 USD / hour
As a Nike Retail Associate - known as Athletes - you bring the “Just Do It” mindset to life. You serve like a pro to help our consumers discover the product that inspires them - from living…
Added 6 mins ago
Product Delivery Associate
JPMC page
Wilmington, DE
…most innovative financial organizations. As a Product Delivery Associate, you will support the delivery of customer-focused capabilities by helping teams plan work, clarify requirements,…
Added 8 mins ago
Pharmacy Technician
Albertsons Companies
REDLANDS, CA · Redlands, CA
Successful completion of required pharmacy training programs and technician development requirements
Added 8 mins ago
Pharmacy Technician
Albertsons Companies
THOUSAND OAKS, CA · Thousand Oaks, CA
Successful completion of required pharmacy training programs and technician development requirements
Added 8 mins ago
Pharmacy Technician
Albertsons Companies
REDLANDS, CA · Redlands, CA
Successful completion of required pharmacy training programs and technician development requirements
Added 9 mins ago
Warehouse Associate - 2nd Shift
Cencora
Shakopee, MN
Added 13 mins ago
Registered Nurse-Emergency Department
Team Member Services
United States
…our Clinical Ladder Program based on experience, professional development, and achievement of advancement…
Added 13 mins ago
Software Engineer Embedded Systems I (Intern) - United States
Cisco
San Jose, CA · Austin, TX · RTP, NC
…Infrastructure & Security. You will be an essential contributor to the development of next-generation innovations in operating systems, firmware, networking stacks, and security…
Added 17 mins ago
CO
Associate Planner
City of South Gate
South Gate, CA
- $43.01 to $52.28 USD / hour
…analyses; may assist in the implementation of the Community Development Block Grant Program; provides information and assistance to developers, the business community, and the public on…
Added 19 mins ago
RV Sales Associate
Blue Compass RV
Cincinnati, OH
We are looking for high-energy, driven Sales Associates to join our team and take ownership of the full sales process from first interaction to final delivery. In this role, you will guide…
Added 19 mins ago
RV Sales Associate
Blue Compass RV
New Carlisle, OH
We are looking for high-energy, driven Sales Associates to join our team and take ownership of the full sales process from first interaction to final delivery. In this role, you will guide…
Added 19 mins ago
RV Sales Associate
Blue Compass RV
Indianapolis, IN
We are looking for high-energy, driven Sales Associates to join our team and take ownership of the full sales process from first interaction to final delivery. In this role, you will guide…
Added 20 mins ago
FF
Part-Time Sales Associate - Famous Footwear
Famous Footwear
KALISPELL, MT
- Part-time
…our team superpower, upholding a work environment where every associate feels included and respected. Maintain a positive and proactive mindset, even in the face of challenges, you’re the…
Added 22 mins ago
Generalist - Maintenance
ACCS
Thomasville, AL
Attends all staff meetings, College meetings, and professional development activities.
Added 22 mins ago
EL
Provider Operations Specialist
Early Learning Coalition of Hillsborough County
Tampa, FL
- $39,228 to $53,081 USD / year
Manage provider contract process from application to execution
Added 23 mins ago
Director of Operations - CRS
Elwyn
Media, PA
…managers. The Director of Operations is also responsible for the development and implementation of policies and procedures, and oversight of program…
Added 23 mins ago
Program Specialist
Elwyn
Upper Chichester, PA
…communicates effectively with all team members, and ensures continuous development and monitoring of programming and services to people on their…
Added 23 mins ago
Incident Coord/Investigator
Elwyn
Monrovia, CA
Reviews the SIR with the appropriate service area Quality Improvement (QI) Specialist (QIS) or Associate Director of QI, where appropriate, for possible support needed in guiding the…
Added 23 mins ago
Registered Nurse (RN)
Elwyn
New Bedford, MA
…impacts their life and how they want to be supported in their process of…
Added 24 mins ago
Equipment Specialist Lead - KS
Panasonic
De Soto, KS
…expertise in equipment troubleshooting, root cause analysis, and process optimization while serving as the primary escalation point for complex equipment-related issues. Working closely…
Added 24 mins ago
Advanced Equipment Specialist - KS
Panasonic
De Soto, KS
…team members while supporting the execution of engineering and process improvement…
Added 24 mins ago
Equipment Specialist - KS
Panasonic
De Soto, KS
Develop working knowledge of assigned production equipment, machine functions, and process operations
Added 24 mins ago
Maintenance Lead Winding, Nights, B-Shift (7PM-7AM)[Sun-Tues + Alt Sat]
Panasonic
Sparks, NV
Must have working-level knowledge of the English language, including reading, writing, and speaking English
Added 25 mins ago
UG
Associate Patient Care Coordinator
UnitedHealth Group
Glendale, CA
- $16 to $29 USD / hour
…inclusion, talented peers, comprehensive benefits and career development opportunities. Come make an impact on the communities we serve as you help us advance health equity on a global…
Added 29 mins ago
Distribution Center Associate
REXEL
Altamont, NY
We are looking for a Distribution Center Associate to join our Rexel, USA team in Albany, NY!

Closed listing

Galderma Laboratories, LP

Regulatory Affairs Associate

United States

$91,200 to $114,000 USD / year

This opening has closed.

The original listing is kept below for reference.

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Job details

Pay: $91,200 to $114,000 USD / year
Experience: 3–7 years of experience in regulatory affairs, with exposure to biologicals, chemical drugs, and/or medical devices.
Posting language: English
Posted: Nov 10, 2026

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Original job description

Archived listing. The details below describe a past opening.

Whether it's the unique breadth of our integrated offering that covers Injectable Aesthetics, Dermatological Skincare and Therapeutic Dermatology products; or our commitment to recognizing and rewarding people for the contribution they make - working here isn't like anywhere else.

At Galderma, we actively give our teams reasons to believe in our ambition to become the leading dermatology company in the world. With us, you have the ultimate opportunity to gain new and challenging work experiences and create an unparalleled, direct impact.

The Opportunity

The Regulatory Affairs Associate supports and implements Regulatory Affairs programs, processes, and policies to support regulatory activities for pharmaceuticals, biologics, chemical drugs, and medical devices. This role coordinates recurring regulatory activities, supports health authority submissions, maintains accurate regulatory documentation and contributes to Drugs CMC regulatory, regulatory operations, and scientific and medical writing.

Working with moderate supervision, the Regulatory Affairs Associate manages routine projects, resolves operational issues and contributes to process improvements including the improvement of regulatory workflows and ensuring timely, accurate submissions. This role also provides junior-level support for the regulatory review of pharmaceutical, biologic, medical device, cosmetic and over the counter products and submission of promotional materials at time of first use.

Key Responsibilities

Build strong, collaborative relationships with internal stakeholders, understanding their needs and providing compliant, practical solutions.
Provide technical guidance to line managers and other colleagues.
Prepare and deliver presentations to business partners or leadership team to communicate regulatory updates and initiatives.

Regulatory Operations and Submissions

Support the administration and Implement of Regulatory Affairs programs, processes, and policies to support regulatory compliance across product categories.
Prepare, review, submit, track and follow up on health authority filings and related regulatory documentation.
Maintain and archive registration files in accordance with applicable procedures and record-retention requirements.
Gather, compile, analyze and summarize data from multiple sources to support submissions, regulatory reports and compliance documentation.
Support CMC regulatory, regulatory operations and medical-writing activities.
Identify operational issues, interpret applicable procedures, and escalate complex matters appropriately.
Contribute to the design and improvement of regulatory workflows, templates, tracking tools and quality controls.

Scientific and Medical Documentation

Draft, edit, format, and review scientific summaries, manuscripts, clinical study reports, monographs, presentations, and other regulatory documents.
Prepare literature for new products and revise existing product materials.
Conduct literature searches and maintains files of journal articles and abstracts for current and anticipated business needs.

Advertising and Promotion

Review derivative materials and second/third round of advertising and promotional materials under the guidance of experienced Regulatory Affairs manager and colleagues.
Compare promotional claims, indications, intended use, safety information, and product descriptions against current approved labeling, instructions for use, and supporting evidence.
Check claims are truthful, accurate, adequately substantiated, and not misleading.
Escalate inconsistent claims to senior reviewers.
Verify the inclusion, accuracy, prominence, and presentation of required safety, risk, limitation, and fair-balance information.
Support the implementation of approved changes and verify that final materials reflect the approved review comments.
Assist with monitoring changes in labeling, scientific evidence, and regulatory requirements that may affect active promotional materials.
Support preparation of applicable advertising and promotional FDA Form 2253 submissions under supervision.

Qualifications

Bachelor’s degree in Regulatory Affairs, Pharmacy, Life Sciences, or a related field, or equivalent experience/qualification.
3–7 years of experience in regulatory affairs, with exposure to biologicals, chemical drugs, and/or medical devices.
Advanced knowledge of regulatory submission processes, documentation standards, and compliance requirements.
Strong technical writing, editing, and document review skills for scientific and regulatory content.
Experience with Drugs CMC regulatory processes, medical writing, and health authority submissions.
Foundational knowledge of pharmaceutical, Over The Counter, Cosmetic and medical device US Advertising and Promotional requirements.
Knowledge of regulatory submissions, documentation standards, product labeling and compliance processes.
Excellent problem-solving skills, with the ability to resolve issues.
Strong organizational skills, attention to detail, and commitment to accurate and timely work.
Ability to manage assignments independently while escalating complex or higher risk matters.
Strong interpersonal skills to build trust and influence across functions.
Proficiency with regulatory information management systems and Microsoft Office Suite.
Detail-oriented with a commitment to accuracy, compliance, and operational efficiency.
Proficient in Microsoft Office Suite, Regulatory Information Management Systems, and electronic review or document-management platforms.

Physical Requirements and Work Environment This role requires the ability to perform standard office activities, including extended periods of computer use, participation in virtual and in-person meetings, and collaboration across teams. Depending on business needs, occasional travel may be required. Work environments and physical requirements may vary based on the requirements of the role. Reasonable accommodations may be made to enable individuals with disabilities to perform the essential functions of the role.

This job description describes the general nature and level of work performed and is not intended to be an exhaustive list of all responsibilities. Duties and responsibilities may be modified, added, or removed as necessary to meet business and organizational needs.

Compensation

The target base salary range for this role is $91,200-$114,000 per year. This range reflects the anticipated compensation for the role. Where pay falls withing the range may vary based on many factors, including, but not limited to, job responsibilities, skills, experience, education, certifications, location and applicable geographic pay zones, market conditions, internal equity and business considerations. Compensation decisions are made based on an assessment of the candidate’s qualifications and the totality of relevant factors.

In addition to base salary, this role is eligible to participate in an annual short-term incentive program, subject to plan terms and eligibility requirements.

Benefits

Galderma offers a competitive and comprehensive benefits program, including medical, dental, and vision coverage, a 401(k) plan with employer match, paid time off, and other benefits, subject to eligibility and applicable plan terms.

Work Authorization This role does not offer sponsorship for work authorization. External applicants must be eligible to work in the United States.

What We Offer At Galderma, you’ll be part of a purpose-driven organization committed to advancing dermatology and improving patient outcomes worldwide. We offer competitive compensation, annual incentive opportunities, and comprehensive benefits, along with meaningful opportunities for growth, development, and collaboration in an inclusive and innovative environment.

Next Steps

If your profile is a match, we will invite you for a first virtual conversation with the recruiter.
The next step is a virtual conversation with the hiring manager
The final step is a panel conversation with the extended team

Don't meet every single requirement? At Galderma, we are dedicated to building a diverse, inclusive, and innovative workplace. If you're excited about this role, but your experience doesn't align perfectly with the qualifications listed, we encourage you to apply anyway!

If you are considering employment at Galderma, review our job postings at www.galderma.com/us/careers. Please be aware of fraudulent job offers and individuals falsely claiming to represent our Human Resources department. Our company will never request or offer payment, personal financial information, or sensitive data (such as Social Security numbers or bank details) during the early stages of recruitment. All legitimate communications from our HR team will come from official company email domains and follow our established hiring process.

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Jobs in the United States