Regulatory Affairs

2 weeks ago


Agoura Hills, United States Brazilian Professionals Full time
Job DescriptionJob Description

The Regulatory Affairs & Documentation Specialist is responsible for formatting, assembling, and timely preparation of documents for domestic and international regulatory submissions and ensuring compliance with applicable regulations.

Assists with technical/regulatory aspects of product development.

Under general supervision of the R&D Department and cross supporting Marketing and Operation Departments, to provide the support required for a successful launch of new & existing products for both domestic and international distribution.

INDUSTRY EXPERIENCE REQUIRED – HAIR CARE, SKIN CARE

Specific Responsibilities & Duties · ·

Manages and prepares documentation for all international product registrations

Stays up to date on all international cosmetic regulations (EU and other territories) including formulations, labeling and packaging related changes.

Maintain all registrations and certificates for all international registrations including CPNP certifications.

Provide correspondence to international distributors on localization matters regarding registration and compliance.

Prepare all related documents required for export registration, i.e. product composition, ingredient SDS, COAs, packaging declarations, manufacturing certificates etc.

Prepare all company finished good SDS documents.

Review regulation changes annually and take any required action ·

Review ingredient list against actual formula to ensure label deck accurately reflects the product content

Creates and maintains technical documentation files for both domestic and international regions. · Obtain technical/regulatory documentation from raw material vendors. ·

Compiles documentation for global product registrations. · Assesses product, manufacturing and labeling changes for regulatory reporting impact and compliance to regulations.

Reviews labeling to ensure compliance with domestic and international standards and regulations and consistency with regulatory submissions/approvals.

Assists with maintenance of processes and procedures related to Regulatory Affairs activities; develops SOP internal procedures and tools. ·

Assists with investigations and executes corrective actions for Quality Incidents (QIs) and Corrective and Preventive Actions (CAPAs) affecting Regulatory Affairs. ·

Organizes and maintains hard copy and electronic department files. · ·

Responds to general product and regulatory inquiries from internal stakeholders

Carries out duties in compliance with established business policies.

Other duties and responsibilities as may be required by the management team.

Physical Requirements · Capable of lifting up to 25 lbs. · Capable of standing, walking, and sitting for extended periods.

Qualifications · High school education or equivalent. · BA/BC of Science; preferably in Chemical, Biochemistry or Microbiology. · 1-3 years experience in Regulatory Affairs in the cosmetic product space.

Contract Manufacturing Experience Preferred.

Knowledgeable with international regulations and be able to prepare documentation & communicate with International regulatory consultants.

Technical Writer. Good oral and written communication skills.

Document Control/Batch Records / Change Control. · Cosmetic ingredient knowledge, INCI. ·

Must have Microsoft Professional edition software skills. ·

Must have project management skills. ·

Knowledge of cGMP of cosmetic products. ·

Demonstration of continual education (through membership in recognized organizations, seminars attended, & certifications.

Strong time-management, organizational, planning people and leadership skills. · Advanced PC Knowledge i.e. MS Office Suite (Excel, Word, Outlook) and management system is required.

Advanced English communications skills: speaking, reading, and writing.

Good interpersonal and customer service skills. · Constantly work to improve processes. · Self-motivated and able to work independently. · Must have cosmetic/OTC product regulatory experience. Work Environment · Office environment. · Noise level is low to moderate. · Proper lighting and ventilation.

Company DescriptionBrazilian Professionals is the exclusive distributor of the original Brazilian Blowout, b3 Brazilian Bond Builder, and b3 Demi Permanent Conditioner.

Brazilian Professionals has focused itself solely in the business of hair, specifically hair treatments.

Our mission is two-fold:

Provide the best in hair treatment innovation to women and men around the world to help them discover hair that fits their lifestyle.

Provide salons and stylists with new service revenue to build their business.Company DescriptionBrazilian Professionals is the exclusive distributor of the original Brazilian Blowout, b3 Brazilian Bond Builder, and b3 Demi Permanent Conditioner.\r
\r
Brazilian Professionals has focused itself solely in the business of hair, specifically hair treatments.\r
\r
Our mission is two-fold:\r
\r
Provide the best in hair treatment innovation to women and men around the world to help them discover hair that fits their lifestyle.\r
\r
Provide salons and stylists with new service revenue to build their business.

  • Arden Hills, Minnesota, United States Boston Scientific Full time

    Recruiter: Spencer Gregory HaleRegulatory Affairs Manager - Core CRM Sustaining Program Regulatory POCTeam Purpose: The Rhythm Management (RM) Regulatory Affairs leadership team is a strategic partner that delivers innovative, efficient, and sustainable business and regulatory solutions for customers throughout the product lifecycle.This role is considered...


  • Arden Hills, Minnesota, United States Boston Scientific Full time

    Recruiter: Spencer Gregory HaleRegulatory Affairs Manager - Core CRM Sustaining Program Regulatory POCTeam Purpose: The Rhythm Management (RM) Regulatory Affairs leadership team is a strategic partner that delivers innovative, efficient, and sustainable business and regulatory solutions for customers throughout the product lifecycle.This role is considered...


  • Laguna Hills, United States Actalent Full time

    Description: This position is a regulatory affairs specialist for a medical device company. Individual must be knowledgeable in medical device industry and have Class II or Class III device experience. Candidate will: Prepare documentation for regulatory submissions and registrations (FDA, EU, and Canada regulatory entities) IDE, PMA, 510(k), Design...


  • Short Hills, New Jersey, United States Varite Full time

    Job Title: Regulatory Affairs Specialist - CMC 2Company: Leading pharmaceutical company in Rahway, NJResponsibilities:- Manage CMC compliance activities and perform Gap Analysis for regulatory requirements- Oversee authoring and review of CMC documentation for life cycle management- Review quality documents such as product development reports and stability...


  • Short Hills, United States Katalyst HealthCares & Life Sciences Full time

    Responsibilities: Well versed in performing CMC compliance activities including Gap Analysis, CMC comparison and validation for the quality reports Experienced in authoring of assessment reports and Part2/ Expert reports for Dossiers Experience in reviewing of quality documents such as Reformulation studies, process validations, particle size...


  • Short Hills, United States Katalyst Healthcares and Life Sciences Full time

    Responsibilities: Well versed in performing CMC compliance activities including Gap Analysis, CMC comparison and validation for the quality reports Experienced in authoring of assessment reports and Part2/ Expert reports for Dossiers Experience in reviewing of quality documents such as Reformulation studies, process validations, particle size method...


  • Arden Hills, Minnesota, United States Boston Scientific Full time

    Additional Location(s): N/ADiversity - Innovation - Caring - Global Collaboration - Winning Spirit - High PerformanceAt Boston Scientific, we'll give you the opportunity to harness all that's within you by working in teams of diverse and high-performing employees, tackling some of the most important health industry challenges. With access to the latest...


  • Arden Hills, Minnesota, United States Boston Scientific Full time

    Additional Location(s): N/ADiversity - Innovation - Caring - Global Collaboration - Winning Spirit - High PerformanceAt Boston Scientific, we'll give you the opportunity to harness all that's within you by working in teams of diverse and high-performing employees, tackling some of the most important health industry challenges. With access to the latest...


  • Far Hills, United States Proxima Full time

    Are you a seasoned Regulatory Affairs professional with a passion for ensuring compliance and driving regulatory strategy in the medical device industry? We're are on the look out for a dynamic Regulatory Affairs Director to lead regulatory initiatives for a one-of-a kind start-up in the Medical Device space. As a key member of the team, you'll play a...


  • Short Hills, United States Varite Full time

    Pay rate range: $40-43/hr. Job Title: CMC 2 Regulatory affairs Location: Rahway, NJ - Onsite Responsibilities: • Well versed in performing CMC compliance activities including Gap Analysis; assessment for Annex 3 comparative table with reference EU Member States • Manage execution / authoring and review of CMC documentation (Module 1 , 2 and 3 / Part II )...


  • Short Hills, United States Varite Full time

    Pay rate range: $40-43/hr. Job Title: CMC 2 Regulatory affairs Location: Rahway, NJ - Onsite Responsibilities: •Well versed in performing CMC compliance activities including Gap Analysis; assessment for Annex 3 comparative table with reference EU Member States •Manage execution / authoring and review of CMC documentation (Module 1 , 2 and 3 / Part II )...


  • Arden Hills, Minnesota, United States Boston Scientific Full time

    Additional Location(s): N/ADiversity - Innovation - Caring - Global Collaboration - Winning Spirit- High PerformanceAt Boston Scientific, we'll give you the opportunity to harness all that's within you by working in teams of diverse and high-performing employees, tackling some of the most important health industry challenges. With access to the latest tools,...


  • Arden Hills, Minnesota, United States Boston Scientific Full time

    Additional Location(s): N/ADiversity - Innovation - Caring - Global Collaboration - Winning Spirit- High PerformanceAt Boston Scientific, we'll give you the opportunity to harness all that's within you by working in teams of diverse and high-performing employees, tackling some of the most important health industry challenges. With access to the latest tools,...


  • Arden Hills, Minnesota, United States Boston Scientific Full time

    Additional Location(s): N/ADiversity - Innovation - Caring - Global Collaboration - Winning Spirit- High PerformanceAt Boston Scientific, we'll give you the opportunity to harness all that's within you by working in teams of diverse and high-performing employees, tackling some of the most important health industry challenges. With access to the latest tools,...


  • Laguna Hills, United States Actalent Full time

    Description: This position is a regulatory affairs specialist for a medical device company. Individual must be knowledgeable in medical device industry and have experience with international submissions and 510k submissions. Candidate will be doing the following: Prepare documentation for regulatory submissions and registrations (FDA, EU, and Canada...


  • Arden Hills, United States Boston Scientific Full time

    Recruiter: Spencer Gregory Hale Regulatory Affairs Manager - Core CRM Sustaining Program Regulatory POC Team Purpose: The Rhythm Management (RM) Regulatory Affairs leadership team is a strategic partner that delivers innovative, efficient, and sustainable business and regulatory solutions for customers throughout the product lifecycle. This role is...


  • Arden Hills, United States Boston Scientific Full time

    Recruiter: Spencer Gregory Hale Regulatory Affairs Manager - Core CRM Sustaining Program Regulatory POC Team Purpose: The Rhythm Management (RM) Regulatory Affairs leadership team is a strategic partner that delivers innovative, efficient, and sustainable business and regulatory solutions for customers throughout the product lifecycle. This role is...


  • Arden Hills, United States Boston Scientific Full time

    Recruiter: Spencer Gregory Hale   Regulatory Affairs Manager - Core CRM Sustaining Program Regulatory POC   Team Purpose: The Rhythm Management (RM) Regulatory Affairs leadership team is a strategic partner that delivers innovative, efficient, and sustainable business and regulatory solutions for customers throughout the product lifecycle.   This...


  • Arden Hills, United States Boston Scientific Full time

    Recruiter: Spencer Gregory Hale   Regulatory Affairs Manager - Core CRM Sustaining Program Regulatory POC   Team Purpose: The Rhythm Management (RM) Regulatory Affairs leadership team is a strategic partner that delivers innovative, efficient, and sustainable business and regulatory solutions for customers throughout the product lifecycle.   This...


  • Arden Hills, United States Boston Scientific Full time

    Recruiter: Spencer Gregory Hale Regulatory Affairs Manager - Core CRM Sustaining Program Regulatory POC Team Purpose: The Rhythm Management (RM) Regulatory Affairs leadership team is a strategic partner that delivers innovative, efficient, and sustainable business and regulatory solutions for customers throughout the product lifecycle. This role is...