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Senior R&D Associate-Regulatory Affairs

Senior R&D Associate-Regulatory Affairs

Requisition #NAM01141

State/Province New Jersey

City Allendale

Position TypeExempt



This is EdgewellWe are a global team of 6,000 visionaries, doers, and makers. Our portfolio of over 25 brands touches lives in more than 50 countries. Together, we re-imagine good mornings and endless summers, beauty and bonding, confidence and determination.
From baby to body, Edgewell is passionate about making the little moments leading up to the big memories just a little bit easier. Simply, we aim to make the products that families rely on more inspired, more personal, and more trustworthy-so they can devote that much more energy to the people they care about most.
We are re-imagining personal care.
At Edgewell Personal Care, we're passionate about helping people be at their best when it matters most: whether preparing for a first date, practicing for the big game, or protecting your family on vacation. The Edgewell family of brands has a product for everyone -- with well-established brand names such as Schick and Wilkinson Sword men's and women's shaving systems and disposable razors; Edge and Skintimate shave preparations; Playtex , Stayfree , Carefree and o.b. feminine care products; Banana Boat and Hawaiian Tropic sun care products; Playtex infant feeding, Diaper Genie and gloves; and Wet Ones moist wipes.

Position SummaryUnder general supervision, provides a variety of routine operations in an office setting. Supports Europe's product notification and registration primarily, followed with a wider scope to support registrations requirements in International Markets when required.

Accountabilities•Draft Cosmetic Product Notifications to the electronic European CPNP portal.
•Compile documents to assemble Product Information Files to support notification submissions and meet compliance to Cosmetic Regulation (EC) No. 1223/2009.
•Help in submitting Product Registrations to European countries outside of the Member States and International countries, including Certificate of Free Sale.
•Compile documents in to assemble technical dossiers to support registration submissions to government authorities.
•Help ensure that products remain in compliance through Gap Analysis and maintain files; route, scan, upload.
•Maintain matrices, log books and tracking sheets.
•Upload / download of product/ingredient information to internal electronic systems.
•Administration: Keep track and maintain up-to-date product registrations data, including registration expirations, discontinuances or product changes. Keep Regulatory database up to date.
•Draft work instructions for routine Regulatory transactions.
•Performs administrative functions as directed by Management to support projects and to ensure the smooth operation of the department.

Required Skills and Experience•Demonstrated work ethic and work experience.
•A degree in the Life Sciences or experience in European/International Regulatory Affairs is a plus but not required.
•A Bachelor's degree in Chemistry is desired but not compulsory.

Preferred Skills and Experience•Good computer skills. Demonstrated proficiency with Word, Excel, databases, e-mail and Internet applications.
• Solid verbal / written communication and interpersonal skills.
• Strong attention to detail.
• Good record-keeping skills.
•Excellent organizational, prioritization and follow-up skills.
•Ability to handle multiple tasks / projects simultaneously.
•Demonstrated ability to complete projects on time.
•Problem-solving skills.
•Ability to sustain quality and accuracy of detailed technical information over long periods of time.
• Some light lifting required, up to 25 pounds.

An Offer to Grow On#LI-JM2




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