Regulatory Affairs Specialist
$80k - $90kMANSCAPED
Job Posting
We have been alerted to the existence of a fraudster impersonating MANSCAPED as a hiring manager or HR representative. This impersonator is utilizing an email address with the domain manscapedjobs.com or manscapedcareers.com and is making fraudulent offers for our open jobs. Contact from MANSCAPED will only ever come from someone with a manscaped.com email address.
This is a scam targeting a number of companies, us included. If you receive any of these types of messages, we recommend that you don't respond with any information and that you block and report those users.
Who We Are - MANSCAPED® is a leading men's grooming and lifestyle consumer brand on a mission to introduce and elevate a whole new self-care routine for men. What began as the category creator of below-the-waist grooming has quickly evolved into a global omnichannel powerhouse available around the world on manscaped.com, Amazon, and in major retailers including Target®, Walmart, and Best Buy. As a company, we're more than just ball jokes (though, rest assured, there's plenty of those). We proudly uphold seven core values – accountability, authenticity, collaboration, fun, humility, inclusivity, and innovation – which define our brand identity and drive our success. As a people-centric employer brand, we are deeply committed to fostering the growth, happiness, and holistic well-being of each individual on our team.
Who We're Looking For - Reporting to the Senior Manager, Regulatory, MANSCAPED® is seeking a Regulatory Affairs Specialist to support global regulatory compliance across current and future markets. This role will help ensure MANSCAPED® products — including cosmetics, personal care formulations, grooming tools, electrical/electronic products, batteries, accessories, and packaging — meet applicable registration, labeling, documentation, certification, claims substantiation, and post-market compliance requirements. The ideal candidate is able to translate technical regulatory requirements into clear guidance as products, markets, and regulations evolve.
The MANSCAPED® Way - At MANSCAPED®, what we do matters – but how we do it matters more. We take ownership of our work, showing up with accountability and a commitment to quality at every level. We work as one team, guided by a belief to unite, never divide, and to lead with empathy in how we support and challenge one another. The best ideas win, and they come from keeping our egos in check and our standards high. We stay humble, open to learning, and willing to grow. We bring fun to the journey, because great work shouldn't come at the expense of enjoying what you do. We stay nimble and innovative, always looking for smarter and better ways to get things done. Ball work is honest work, and that mindset shows up in everything we do, including our proud partnership with the Testicular Cancer Society and our commitment to raising awareness of the ball-busting disease.
Responsibilities:
- Support the development and execution of regulatory strategy to maintain MANSCAPED product compliance across the US and international markets
- Collect, review, and maintain regulatory documentation (testing reports, ingredient documents, raw material, product specifications, SDS, and certifications) and maintain Product Information Files (PIFs)
- Support the reviewal process for claims and product substantiation guidelines
- Stay abreast of international regulatory legislation, guidelines, and certification processes, and assist with ongoing regulation monitoring
- Support cross-functional teams regarding documents, regulation guardrails, and internal processes
- Assist with registration, assessments and reporting needs for Extended Producer Responsibility (EPR)
- Maintain regulatory archives, and product information and registration databases
- Help develop and maintain Standard Operating Procedures (SOPs) that support the regulatory function
- Assist with regulatory-related questions from internal and external partners
- Help ensure products meet regulatory requirements for current markets and future markets tied to MANSCAPED's global expansion roadmap, including labeling considerations
- Serve as a regulatory resource throughout the product lifecycle, translating technical requirements into clear guidance as products, markets, and regulations evolve
- Other duties as required
Qualifications:
- Bachelor's degree in Chemistry, Biological Sciences, Biochemistry, Cosmetic Science Regulatory Affairs or related field
- 2 + years of experience in regulatory affairs, preferably within the cosmetics, personal care, beauty, or consumer products industry. Hands-on experience with supporting global regulatory compliance documentation including MoCRA, EU (EC1223/2009), and other related state and international cosmetics regulations is preferred
- Strong documentation skills, with experience organizing and maintaining regulatory files and records
- Experience managing multiple projects simultaneously with strong time management skills
- Excellent written and verbal communication abilities
- Technical curiosity and process-driven mentality
- Collaborative, resourceful, and ability adapt to an evolving atmosphere
MANSCAPED® Benefits
- Take time to find balance and rejuvenate your senses. Enjoy a generous 20 accrued vacation days per year to relax, travel, and spend quality time with your loved ones. We value your need for a healthy work-life balance
- Health comes first, always. We provide 40 hours of paid sick leave annually, ensuring you can take the time you need to recover
- Your mental health matters. Take 3 paid mental health days to recharge and take care of your emotional well-being
- We offer 9 paid holidays throughout the year to give you the opportunity to celebrate important moments and take a break from work
- Some call it pet insurance, we call it Paws & Claws coverage. Our plan helps you take care of your furry family members, giving you peace of mind
- Our comprehensive life insurance, AD&D and long-term disability coverage provide financial security for you and your family in case of unexpected events
- Access comprehensive medical, dental, and vision insurance plans, along with Health Savings Accounts (HSA) and Flexible Spending Accounts (FSA), ensuring you and your family are well-covered
- If you're facing life's challenges, our confidential Employee Assistance Program offers resources to help you navigate them
- Add a layer of protection from the unexpected costs of emergencies and unexpected illnesses. Enrollment in our accident and critical illness plans can provide financial support during the most difficult of times
- Let us take the guess work out of retirement planning with our employee 401(k) plan and company match
- We are a remote-first employer. You will receive a monthly utility allowance to help cover the costs of Wifi and phone usage
- Enjoy a generous discount on our products as part of our employee discount program, making holiday and birthday shopping a breeze
- Participate in our exciting wellness challenges designed to promote a healthy and active lifestyle. From step competitions to mindfulness sessions, join your colleagues in fun and motivating activities that boost your physical and mental well-being
- We support our families by offering paid parental leave to support you during a pivotal time in your life, adding to the family!
- We like to cheer each other on. Our regular recognition initiatives ensure you are acknowledged for your hard work and achievements
- We encourage community involvement by offering one paid volunteer day per year, allowing you to support a cause that means the most to you
- We are a certified Great Place to Work, growing rapidly and offering incredible opportunities for advancement. Join us and be part of an exciting journey with a company that values its employees
Compensation Range $80,000 —$90,000 USD
$85k - $125k
...supplier of high-quality Lentiviral vectors for research and clinical use. We are seeking an exceptional team member to provide regulatory and product development support in a dynamic small company setting. If you are comfortable on the cutting edge and passionate about...SuggestedFor subcontractor$38 - $56 per hour
...LHH Recruitment Solutions is seeking a Regulatory Affairs Specialist for a minimum 6-month remote contract opportunity. This position is open to candidates residing in California who have prior experience in the medical device industry. The ideal candidate will have a...SuggestedHourly payContract workLocal areaImmediate startRemote workMonday to Friday- ...Regulatory Affairs Specialist Job Type: Full time - Permanent Location: Madison, New Jersey (On-site) A commercial-stage transplant technology company, part of a global medtech group, is changing how donor organs are preserved and assessed before transplant. Their...SuggestedPermanent employmentFull time
- ...Insight Global is looking for a Regulatory Affairs Specialist that will be responsible for the regulatory functions including support of labeling requirements, serving as regulatory representative on selected project teams. You will also support compilation and submission...Suggested
- ...QMS Consulting seeks a Regulatory Specialist with direct experience drafting federal rules for the a federal agriculture agency. The specialist will serve as a rulemaking subject matter lead for up to three proposed-rule efforts. Working with QMS analysts and federal...SuggestedPermanent employmentFull time
- The Regulatory Affairs Level III (Senior Specialist) position is responsible for global product registrations and ensuring regulatory compliance in the design, manufacturing, and sales of medical devices (including Class I and II devices, software as a medical device, and...
- Job-ID32758545Reference26-01317Remote50% Remote Job Description: Highly experienced Principal Regulatory Affairs Specialist to lead and support global post-market regulatory compliance activities within the Interventional Cardiology and Vascular Therapies Division. This...Remote work
- ...provides flexibility to work 4 days on site and Friday remotely on a weekly basis in Covington, GA. *** Job DescriptionThe Regulatory Affairs Specialist II is responsible for implementation of regulatory strategies including domestic and international submissions and other...Full timeWork at officeRemote workDay shift
- ...is working in the CMC area. Relevant experience is requiredExperience: 3 to 6 yearsExperience with drug/biologics licensurePrior regulatory experienceTechnical writing experience (CMC experience )Scientific background,Required Skills:CMC/ Regulatory writing experienceScientific...Work at officeImmediate start
- Job-ID31525652Reference25-04486 Responsibilities: The Regulatory Affairs Specialist is responsible for working with cross-functional teams to bring IVD (In-Vitro Diagnostic), Research (RUO) and Laboratorial products to market and support activities related to Quality...
- The Regulatory Affairs Specialist 3 develops and executes regulatory strategy and integrates regulatory requirements throughout the product lifecycle. Relies on extensive experience and judgment to plan, create, develop and maintain materials needed for regulatory compliance...
$77k - $128.3k
...communities, and our people. If you want to be part of tomorrow’s health today, we want to hear from you.Position Summary The Regulatory Affairs Manager (P3), Complex Molecules & Specialized Distribution Programs, supports regulatory compliance for pharmaceutical...Full timeWork at office- ...both internal and external cross-functional project teams.• The Regulatory CMC Technical Associate may be called upon to author technical... ...Master s Degree a plus• 4+ years of pharmaceutical regulatory affairs experience• Strong knowledge of NDA, ANDA, MAA, BLA, CTA, or...Work at officeLocal areaImmediate start
$107.2k - $160.8k
...font-size: 30px; font-weight: bold; width: 883px; left: 5px; height: 72px; padding-left: 17px; padding-top: 15px; } he Regulatory Affairs Specialist is responsible for day-to-day regulatory affairs tasks required to maintain compliance with Coloplast’s quality system and...Work at officeLocal areaImmediate startFlexible hours- ...financial flexibility by offering contingent labor as a variable cost.Job DescriptionThis individual will be part of the Global Regulatory Affairs team and assists with planning, writing, compilation, and editing of periodic regulatory reports (i.e. DSURs, orphan annual...Work at officeImmediate start
$90k - $125k
Alameda, CAGeneral Administration - Regulatory Affairs /External /HybridIn this role, you will work with the team that ensures that Penumbra products are approved for use in countries around the world, thereby helping to bring our life-saving technologies to patients worldwide...Temporary workWork at officeLocal areaWorldwide- Brecksville, OHDescriptionJob Title: Regulatory Affairs SpecialistDepartment: RegulatoryReports To: Director of Regulatory AffairsFLSA Status: ExemptSupervise the work of others: NoPosition Summary:This position is responsible for preparing submissions to various regulatory...Work experience placementWork at office
- ...solutions. We have a robust product portfolio and pipeline and continue to invest in urology treatments.This role is responsible for Regulatory Affairs support for submissions and ongoing regulatory compliance throughout the product development process. The role will also...Hourly payContract workWork at officeLocal areaRelocationRelocation packageShift work3 days per week
- ...Responsibilities: This position is responsible for the preparation of regulatory submissions required to market medical devices in both the U.S... ...of international product registrations and related regulatory affairs activities, including execution of procedures and systems...Work at office
- Job-ID31824874Reference26-00210 Responsibilities: The Regulatory Affairs Level III (Senior Specialist) position is responsible for global product registrations and ensuring regulatory compliance in the design, manufacturing, and sales of medical devices (including Class...
- The Compliance Specialist reports to the Director Legal, Compliance, Privacy & Security (“Director”) and has a key role in supporting the... ...basis.Conduct research and develop written communication on regulatory requirements to ensure ongoing updates upon request. Manage compliance...Contract work
- ...healthcare, developing complete solutions which optimize the urine drainage process in the Acute Care Hospital setting. The Regulatory Affairs Specialist I is responsible for implementation of regulatory strategies including domestic and international submissions and other...Full timeWork at officeRemote workDay shift
- ...execution phases, and provide budgeting/financial flexibility by offering contingent labor as a variable cost.Job Description• The Regulatory Affairs Operations (RA Ops) submission group is organized to provide submission development support to project teams and the...Immediate start
- ...medical technology or similar. 5+ years of experience in Reg Affairs, QA, R&D, Manufacturing, and/or Project Management within the... ...verbal and written communication skills. Thorough knowledge of policies, practices and procedures related to Regulatory Affairs.
- ...439Reference25-02134 Responsibilities: Contributes to the FDA regulatory submission process; may aid in authoring and/or publishing electronic... ...equivalent). A minimum of 3 years' experience in Regulatory Affairs Advanced experience in the areas that may include preparation...Work at office
$70k - $95k
...Job Title Industry Regulatory Affairs Job Type FT-Days Location REMOTE OPTION Salary $70,000 - $95,000 Job Description Responsibilities in this position will include: Supports preparation and maintenance of program annual reports, and may support...Contract workWork at officeRemote work- ...Regulatory Submission Coordinator Role Summary: Responsible for global coordination and preparation of regulatory submission documents... ...Experience with medical devices / healthcare regulatory affairs. Knowledge of U.S. and OUS device regulations, especially EU...Remote work
- ...Regulatory Affairs Specialist We are seeking a detail-oriented and experienced Regulatory Affairs Specialist to join our team in Canada. The successful candidate will be responsible for ensuring compliance with Canadian regulatory requirements for our products, working...Work at officeRemote work
- ...Regulatory Affairs Specialist Are you ready to accelerate your potential and make a real difference within life sciences, diagnostics and biotechnology? At Masimo, one of Danaher's 15+ operating companies, our work saves lives—and we're all united by a shared commitment...Work experience placementLocal areaRemote workWork from homeFlexible hours
$65k - $75k
...Pay: $65,000.00 - $75,000.00 per year Job description: Position Summary We are seeking a Junior Regulatory Affairs professional to support regulatory compliance for personal care and hair care products across domestic and international markets. The incumbent of...Contract workWork at officeLocal areaRemote workFlexible hours
Do you want to receive more vacancies?
Subscribe and receive similar vacancies to Regulatory Affairs Specialist. Be the first to apply!
- corporate compliance officer United States
- research regulatory specialist United States
- financial compliance analyst United States
- compliance business analyst United States
- compliance support specialist United States
- junior regulatory affairs specialist United States
- product compliance specialist United States
- compliance analyst United States
- aml compliance analyst United States
- entry level compliance officer United States



