Regulatory Affairs/ Quality Assurance Summer Intern
Company
Unilever
Location
Gunnison, CO / Remote
Type
Full Time
Job Description
ROLE DESCRIPTION
Regulatory Affairs/Quality Assurance (RA/QA), HEALTH & WELLBEING
Manager level: Intern
Schedule: Summer 2024
Location: USA - Englewood Cliffs
Function: Regulatory Affairs
Reports to: TBD
WHO ARE WE?
We are the Global Health & Wellbeing (H&W) team at Unilever. We are focused on one of Unilever's largest growth opportunities - the €140bn Health & Wellbeing space defined by Vitamins, Minerals, and Supplements (VMS).
We work in an agile and entrepreneurial way, collaboratively within the team and with our Unilever colleagues around the world. We work in a project based networked way where everyone needs to be able to take a step back and think strategically as well as rolling up their sleeves and get their hands dirty, to be entrepreneurial and experiment as well as bringing in the best of Unilever and work the structures of a large company, to take charge and lead as well as follow and support others.
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OUR BUSINESS
Unilever's Health & Wellbeing Group holds the company's functional nutrition brands and the portfolio of brands that includes Equilibra (Italy) and US acquired brands Olly, LiquidIV, SmartyPants, Welly, Onnit and Nutrafol. Each brand is completely unique and focused on giving consumers superior experiences within their respective spaces and target segments. We are committed to continue to grow this strategic business for Unilever through a series of acquisitions and international expansion of acquired brands through Unilever's scale and network in the markets.
JOB DESCRIPTION OVERVIEW
The RA/Q interns will play a critical role in the H&W regulatory & quality team. The intern will be responsible for helping build out the RA/QA compliance initiatives.
The intern will learn how Regulatory Affairs or Quality Assurances functions as a true business partner to protect and grow brands to help underpin them as leaders in the industry. A true passion for learning and science is a must.
POTENTIAL KEY ACCOUNTABILITIES (RA or QA)
- Learning how Regulatory drives FDA/FTC compliance
- Formula Dossiers/Raw Material requirements
- Label Claims & Substantiation - Risk vs Commercial Success
- FDA Inspection Readiness
- Working on the Quality Management Systems (QMS) to ensure FDA compliance
- Analytical Testing (Stability/Release)
- SOP's/GMP Docs
- Learning about GMP Quality Audits (External and Internal)
- Quality Agreements/Supplier Management
- Student currently in a Bachelor Program in Chemistry, Biology, or comparable life science degree
- Broad knowledge and interest FDA, Regulatory Affairs and/or Quality Assurance
- Ability to protect IP-generation from within Unilever
- Excellent written and verbal communication skills and ability to present information in a clear and concise manner
- Problem-solving, troubleshooting skills and ability to find creative solutions
- Ability to work successfully both independently and in a 'team-based' collaborative environment
For more information about your Federal rights, please see Know Your Rights: Workplace Discrimination is Illega l and Pay Transparency Nondiscrimination Provision .
Employment is subject to verification of pre-screening tests, which may include drug screening, background check, credit check and DMV check.
If you are an individual with a disability in need of assistance at any time during our recruitment process, please contact us at [email protected] . Please note: This email is reserved for individuals with disabilities in need of assistance and is not a means of inquiry about positions or application statuses. The Protected Veterans or Individuals with Disabilities AAP narratives are available for inspection by any employee or applicant for employment Monday through Friday during normal business hours at establishment.
#LI-Remote
Date Posted
10/12/2024
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