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Regulatory Affairs Associate Skincare

Collabera

  • Irvine
  • 5 days ago
  • $34–$38 Per Hour
  • Temporary
  • Contractor

Highlights

Major Responsibilities: Reviews product labeling for accuracy and for other legal/regulatory requirements and communicates planned/approved changes with other functions, including but not limited to operations, medical affairs and commercial teams. Generates Origin, Animal testing, Allergens, CMR/Nano, Gluten Free, BSE and other requested statements upon review of formula or ingredients.
Collabera

Numbers & Facts

LocationIrvine
Job TypeTemporary, Contractor
IndustryStaffing/Employment Agencies
Salary$34–$38 Per Hour
Company Size10,000 employees or more
Year Founded1991
Websitehttp://www.collabera.com

Description

Position Details:

Client Industry: Pharmaceutical/Medical Device/Biotechnology
Title: Regulatory Affairs Associate I – Skincare
Location: Irvine, CA 92612 – Hybrid 
Duration:  12-month Contract 
Shift: USA Standard Business Hours Shift
Pay Rate: $34.00 – $38.00 per hour 
 
Job Details:
Note : Local Candidates only. Manager is not interested in candidates that will need to relocate.
 
What are the top 3-5 skills, experience or education required for this position:
  • Ability to critically and effectively review detailed information to support a labelling revision including all applicable regulations.
  • Ability to manage multiple priorities and projects with strict deadlines
  • Detail-oriented with the ability to proofread and check documents for accuracy and consistency.
  • Excellent communication skills
Purpose Statement:
The Regulatory Affairs Associate I support the development and implementation of the global regulatory strategy for SkinMedica products. With supervision, the specialist reviews, plans and prepares regulatory documents and labelling for cosmetic or OTC product registrations/updates. With supervision, the specialist researches and interprets health authority regulations/guidance and provides regulatory information to cross-functional teams, as appropriate.
 
Major Responsibilities:
  • Reviews product labeling for accuracy and for other legal/regulatory requirements and communicates planned/approved changes with other functions, including but not limited to operations, medical affairs and commercial teams.
  • Provides regulatory guidance to other departments as needed to ensure compliance with regulations.
  • Conducts regulatory assessments of product changes, labeling revision, and new product introduction.
  • Review international regulations to assess and support market expansion feasibility.
  • Monitor and track federal, state, and international regulatory developments relevant to the organization’s business and operations.
  • Generates ingredient list (IL) and Cosmetic or OTC formulation assessments.
  • Reviews and approves formulations and labeling for local and global compliance.
  • Generates Origin, Animal testing, Allergens, CMR/Nano, Gluten Free, BSE and other requested statements upon review of formula or ingredients.
  • Acquires necessary regulatory documentation from Raw Material suppliers.
  • Provides insight to formulators to create global and local compliant formulations.
  • Prepares and submits regulatory documents for cosmetic registration and responds to other regulatory questions as needed.
  • Ensures archiving of activities, especially submissions, internal memos and key correspondence.
  • Monitors and interpret regulatory requirements and guidelines and assesses impact on SkinMedica products.
  • Notifies relevant cross-functional team members of regulatory activities, as appropriate.
  • Provides status updates to management.
Qualifications:
  • Basic knowledge of personal care product industry regulatory affairs discipline throughout the product lifecycle including development, commercialization and operations.
  • Ability to critically and effectively review detailed information to support a labelling revision including all applicable regulations.
  • Ability to manage multiple priorities and projects with strict deadlines
  • Working knowledge of the OTC drug monographs and cosmetics.
  • Detail-oriented with the ability to proofread and check documents for accuracy and consistency.
  • Excellent communication skills.
  • Strong interpersonal skills with the ability to influence others in a positive and effective manner.
  • Ability to understand and apply business drivers outside of Regulatory Affairs.
Education
  • BS degree in a scientific field, plus two years’ experience in regulatory affairs; or equivalent relevant work experience.
  • MS degree in a scientific field, plus one year experience in regulatory affairs; or equivalent relevant work experience.
  • PhD degree in a scientific field, with no experience in regulatory affairs.
Benefits:
The Company offers the following benefits for this position, subject to applicable eligibility requirements: medical insurance, dental insurance, vision insurance, 401(k) retirement plan, life insurance, long-term disability insurance, short-term disability insurance, paid parking/public transportation, (paid time , paid sick and safe time , hours of paid vacation time, weeks of paid parental leave, paid holidays annually – These all are subject to applicable eligibility).

About Company

Since 1991, Collabera has been a leading provider of IT staffing solutions and services. We are known for providing the best staffing experience and taking great care of our clients and employees.

Our client-centric model provides focus, commitment and a dedicated team to help our clients achieve their business objectives. For consultants and employees, we offer an enriching experience that promotes career growth and lifelong learning.

The Collabera Way represents our fundamentals beliefs and is founded on the following building blocks:
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