drjobs Manager Regulatory Affairs

Manager Regulatory Affairs

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1 Vacancy
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Job Location drjobs

New York City, NY - USA

Monthly Salary drjobs

Not Disclosed

drjobs

Salary Not Disclosed

Vacancy

1 Vacancy

Job Description

Responsibilities:
  • The Manager Regulatory Affairs will be responsible for managing regulatory requirements and inmarket product compliance to maintain and further develop the regulatory capability of the USbased regulatory team for Alchemee (previously The Proactiv Company).
  • The Manager Regulatory Affairs serves as the domestic and global regulatory contact at Alchemee.
  • This role is expected to establish and build a full collaborative partnership with internal teams in support of Alchemee business needs.
  • This role will provide leadership in identifying regulatory and legislative issues that have the potential to impact the development and marketing of products.
  • Provides strategic input and tactical support to project teams throughout the product lifecycle with the goal of empowering informed decisionmaking to bring products to the market and maintain their availability.
  • Lead US OTC and Cosmetic and global regulatory functions and partner with business to drive growth ambition.
  • Serving as the Regulatory representative on specific multidiscipline teams may be responsible for organizing and leading meetings.
  • Establishes efficient integration of regulatory support into R&D technology/product development marketing and business processes.
  • Ensures all governmental reporting systems and documentation comply with applicable regulatory standards and requirements for OTC drug cosmetic consumer and other products.
  • Work with internal and external companies to ensure appropriate regulatory framework is in place to ensure endtoend regulatory compliance (e.g. cGMP labeling advertisement/promotional claims etc.
  • Provides regulatory management and interface with regulatory authorities in case of issues audits quality incidents market recalls and any regulatory challenges.
  • Lead with legal counsel to resolve product compliance conflicts and other issues when ambiguity exists in the regulations by applying risk management principles to ensure consumer and brand protection.
  • Manages the regulatory affairs associates daily workload; including dossiers PIFs filing of license applications product registrations renewals and annual reports with regulatory agencies when required.
  • Provides regulatory guidance as it relates to retail direct to consumer business to business and WERCs.
  • Oversee FDA detention holds custom holds and border patrol and/or port product hold issues.
Requirements:
  • Bachelors degree in chemistry Applied Science or related field required.
  • Five to Eight years of experience in the regulatory function on cosmetic/personal care skin care pharmaceutical or manufacturing industry experience.
  • Demonstrated leadership skills in the areas of managing teams driving results team collaboration mentoring and coaching problem solving and communication across functional areas.
  • Working knowledge of products formula (INCI) regulatory labeling and claims for OTC monograph products and skincare cosmetics including federal state consumer product safety commission and EPA.
  • Strong knowledge/application of US FDA regulations Health Canada regulations EU/Brexit regulations Japan (MHLW) regulations PMDA Prop 65 guidance documents and validation requirements.
  • Expertise in Cosmetic/OTC raw material ingredients safety and regulations.
  • Demonstrated ability to work independently and practically handle multiple tasks simultaneously prioritize negotiate and meet critical timelines.
  • High proficiency with software applications like Excel PowerPoint Word PLM QMS systems and PCPC.
  • Experience in international product introductions including international compliance global product and formula percent limitations and release requirements.
  • Provide regulatory guidance risk assessment and management throughout the product lifecycle: New Product Development and Commercial projects.
  • Providing input to Standard Operating Procedure documents to ensure accuracy and compliance as appropriate.

Employment Type

Full Time

Company Industry

About Company

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