Regulatory Quality Specialist

12 hours ago

Florham Park, United States Insight Global Full time

Professional Recruiter | Insight Global | Pennsylvania State University Alumni Regulatory Site Quality Specialist JOB DESCRIPTION A large CPG client of ours is looking for a regulatory site quality specialist to help with their products OTC drug listing portfolio. This role is responsible for managing the drug listing process, including the listing and delisting of products (skincare, cosmetics). The position supports regulatory tasks and regulatory operations as needed, while collaborating with cross‑functional teams on the initiation, review, and approval of change requests, deviations, and CAPAs. Key responsibilities include reviewing and approving incoming raw material documentation, LIMS specifications, and Certificates of Analysis, as well as GMP batch records, packaging protocols, clinical labeling records, and analytical laboratory documentation such as test methods, protocols, and reports. The role also involves participating in internal audits as a scribe and document reviewer, providing GMP consultation to project teams and departments, and serving as a backup for the QA Manager. REQUIRED SKILLS AND EXPERIENCE BS degree in science or engineering 5 years' experience in Regulatory, Quality, R&D or Analytical in a GMP facility Experience and understanding of FDA OTC Drug Listing Process Experience and understanding GMP Procedures Experience with SOPs, deviations, change controls, CAPAs Detail Oriented, Organized OTC Drug or Cosmetics Experience NICE TO HAVE SKILLS AND EXPERIENCE LIMS experience Cosmetics or skincare experience #J-18808-Ljbffr

  • Regulatory Quality Specialist

    2 weeks ago

    Florham Park, United States Insight Global Full time

    Professional Recruiter | Insight Global | Pennsylvania State University Alumni Regulatory Site Quality Specialist JOB DESCRIPTION A large CPG client of ours is looking for a regulatory site quality specialist to help with their products OTC drug listing portfolio. This role is responsible for managing the drug listing process, including the listing and...

  • Regulatory Quality Specialist

    4 weeks ago

    Florham Park, United States Insight Global Full time

    Year Long Contract 2 Hire ***********************************Regulatory Site Quality SpecialistJOB DESCRIPTIONA large CPG client of ours is looking for a regulatory site quality specialist to help with their products OTC drug listing portfolio. This role is responsible for managing the drug listing process, including the listing and delisting of products...

  • OTC Regulatory Quality Lead – GMP

    2 weeks ago

    Florham Park, United States Insight Global Full time

    A prominent staffing firm is seeking a Regulatory Site Quality Specialist in Florham Park, NJ. The role involves managing the OTC drug listing portfolio, participating in regulatory tasks, and collaborating across teams. Key qualifications include a BS degree in science or engineering and at least 5 years of experience in a GMP environment. Candidates should...

  • OTC Regulatory Quality Lead – GMP

    10 hours ago

    Florham Park, United States Insight Global Full time

    A prominent staffing firm is seeking a Regulatory Site Quality Specialist in Florham Park, NJ. The role involves managing the OTC drug listing portfolio, participating in regulatory tasks, and collaborating across teams. Key qualifications include a BS degree in science or engineering and at least 5 years of experience in a GMP environment. Candidates should...

  • Regulatory Affairs Associate

    2 weeks ago

    Florham Park, United States Insight Global Full time

    Regulatory Site Quality SpecialistLocation: hybrid (Florham Park, NJType: Contract | Full-TimeIndustry: Large Consumer Packaged Goods (CPG) CompanyJob OverviewWe are seeking a Regulatory Site Quality Specialist to support a leading CPG company's OTC drug listing portfolio. This role will manage the drug listing process for skincare and cosmetic products,...

  • Regulatory Affairs Associate

    2 weeks ago

    Florham Park, United States Insight Global Full time

    Regulatory Site Quality SpecialistLocation: hybrid (Florham Park, NJType: Contract | Full-TimeIndustry: Large Consumer Packaged Goods (CPG) CompanyJob OverviewWe are seeking a Regulatory Site Quality Specialist to support a leading CPG company’s OTC drug listing portfolio. This role will manage the drug listing process for skincare and cosmetic products,...

  • Regulatory Affairs Associate

    1 week ago

    Florham Park, United States Insight Global Full time

    Regulatory Site Quality SpecialistLocation: hybrid (Florham Park, NJType: Contract | Full-TimeIndustry: Large Consumer Packaged Goods (CPG) CompanyJob OverviewWe are seeking a Regulatory Site Quality Specialist to support a leading CPG company’s OTC drug listing portfolio. This role will manage the drug listing process for skincare and cosmetic products,...

  • Regulatory Affairs Associate

    2 weeks ago

    Florham Park, NJ, United States Insight Global Full time

    Regulatory Site Quality Specialist Location: hybrid (Florham Park, NJ Type: Contract | Full-Time Industry: Large Consumer Packaged Goods (CPG) Company Job Overview We are seeking a Regulatory Site Quality Specialist to support a leading CPG company's OTC drug listing portfolio. This role will manage the drug listing process for skincare and cosmetic...

  • Regulatory Affairs Associate

    2 weeks ago

    Florham Park, NJ, United States Insight Global Full time

    Regulatory Site Quality Specialist Location: hybrid (Florham Park, NJ Type: Contract | Full-Time Industry: Large Consumer Packaged Goods (CPG) Company Job Overview We are seeking a Regulatory Site Quality Specialist to support a leading CPG company’s OTC drug listing portfolio. This role will manage the drug listing process for skincare and cosmetic...

  • Regulatory Compliance Specialist

    2 weeks ago

    Florham Park, United States ADP Full time

    A leading provider of human capital management solutions is seeking a Compliance Administrator to ensure compliance with regulatory requirements and manage registration data. Responsibilities include scheduling exams, processing filings, and coordinating with vendors. The ideal candidate has strong attention to detail, organizational skills, and at least 2...