Actalent
Regulatory Affairs Specialist
Actalent, Piscataway, New Jersey, us, 08854
Job Title: Regulatory Affairs Specialist
Job Description
Assist in the creation and update for new and existing products and ensure consistency of label with the master manufacturing formula and compliance with all applicable cosmetic supplement labeling regulations. Accurately establish and implement all relevant information that must appear on a finished product label utilizing the correct format according to regulatory guidelines. Implement the necessary changes to any existing finished product labels due to product reformulation or ingredient/supplier change. Review, approve and provide finished product regulatory documents based on customers' requirements or requests. Maintain and organize files for online and hard copy product label Master Copy book. Assist in gathering and reviewing raw materials documents and ensure the minimal required documents are provided by raw material vendors on time before the panel is finalized/approved and that all other documents are requested, received and filed. Review and approve or reject customer labels, make suggestions, if needed, to rectify any errors to ensure compliance with all pertinent labeling regulations. Maintain excel sheets, used to create Nutrition/Supplement Facts, and ensure nutritional data and other information entered in the system are correct, complete and in compliance with pertinent labeling regulations. Assist in and ensure the timely and accurate completion of documents (Product Data Sheet, Allergen Statement, BE/GMO statement, etc.) and other regulatory requests and inquiries from external customers and from other departments in the company related to labeling compliance, product and ingredients information and documentation.Hard SkillsBachelors degree in Sciences-ChemistryCosmeticsChemical Engineering (preferred)3-5 Years of experience in Labellinglaboratory safetySDS management (safety data sheet)Chemical manufacturing industry, (cosmetic preferred)Job Type
This is a Contract-to-Hire position with a duration of 6 Month(s).Work Site
This is a fully on-site position in Piscataway, New Jersey.About Actalent
Actalent is a global leader in engineering and sciences services and talent solutions. We help visionary companies advance their engineering and science initiatives through access to specialized experts who drive scale, innovation and speed to market. With a network of almost 30,000 consultants and more than 4,500 clients across the U.S., Canada, Asia and Europe, Actalent serves many of the Fortune 500.Diversity, Equity & Inclusion
At Actalent, diversity and inclusion are a bridge towards the equity and success of our people. DE&I are embedded into our culture through:Hiring diverse talentMaintaining an inclusive environment through persistent self-reflectionBuilding a culture of care, engagement, and recognition with clear outcomesEnsuring growth opportunities for our people
The company is an equal opportunity employer and will consider all applications without regard to race, sex, age, color, religion, national origin, veteran status, disability, sexual orientation, gender identity, genetic information or any characteristic protected by law.
If you would like to request a reasonable accommodation, such as the modification or adjustment of the job application process or interviewing process due to a disability, please email actalentaccommodation@actalentservices.com for other accommodation options.
Job Description
Assist in the creation and update for new and existing products and ensure consistency of label with the master manufacturing formula and compliance with all applicable cosmetic supplement labeling regulations. Accurately establish and implement all relevant information that must appear on a finished product label utilizing the correct format according to regulatory guidelines. Implement the necessary changes to any existing finished product labels due to product reformulation or ingredient/supplier change. Review, approve and provide finished product regulatory documents based on customers' requirements or requests. Maintain and organize files for online and hard copy product label Master Copy book. Assist in gathering and reviewing raw materials documents and ensure the minimal required documents are provided by raw material vendors on time before the panel is finalized/approved and that all other documents are requested, received and filed. Review and approve or reject customer labels, make suggestions, if needed, to rectify any errors to ensure compliance with all pertinent labeling regulations. Maintain excel sheets, used to create Nutrition/Supplement Facts, and ensure nutritional data and other information entered in the system are correct, complete and in compliance with pertinent labeling regulations. Assist in and ensure the timely and accurate completion of documents (Product Data Sheet, Allergen Statement, BE/GMO statement, etc.) and other regulatory requests and inquiries from external customers and from other departments in the company related to labeling compliance, product and ingredients information and documentation.Hard SkillsBachelors degree in Sciences-ChemistryCosmeticsChemical Engineering (preferred)3-5 Years of experience in Labellinglaboratory safetySDS management (safety data sheet)Chemical manufacturing industry, (cosmetic preferred)Job Type
This is a Contract-to-Hire position with a duration of 6 Month(s).Work Site
This is a fully on-site position in Piscataway, New Jersey.About Actalent
Actalent is a global leader in engineering and sciences services and talent solutions. We help visionary companies advance their engineering and science initiatives through access to specialized experts who drive scale, innovation and speed to market. With a network of almost 30,000 consultants and more than 4,500 clients across the U.S., Canada, Asia and Europe, Actalent serves many of the Fortune 500.Diversity, Equity & Inclusion
At Actalent, diversity and inclusion are a bridge towards the equity and success of our people. DE&I are embedded into our culture through:Hiring diverse talentMaintaining an inclusive environment through persistent self-reflectionBuilding a culture of care, engagement, and recognition with clear outcomesEnsuring growth opportunities for our people
The company is an equal opportunity employer and will consider all applications without regard to race, sex, age, color, religion, national origin, veteran status, disability, sexual orientation, gender identity, genetic information or any characteristic protected by law.
If you would like to request a reasonable accommodation, such as the modification or adjustment of the job application process or interviewing process due to a disability, please email actalentaccommodation@actalentservices.com for other accommodation options.