Regulatory Affairs Assistant

Industry

Manufacturing and Production

Advert ID

USA_401796

Location

Englewood Cliffs

Job Type

Contract

Hours

Full-Time

Salary Range

Up to USD30.00/hr

No. of Openings

1

Branch Information

Hackensack, NJ - (USA) 505 Main St NJ Hackensack , NJ - 07601 Phone : 201-342-6962

ContactNumber

201-342-6962

Job Description

Specification Writer ' Hr ' USD ' US Description: Regulatory Affairs Assistant - Cluster Product Compliance (CPC) Position Summary: To work with the RA Cluster Product Compliance Team to review raw material data between two software systems which is needed to deliver raw material specifications that are compliant with local and global specifications. Position Responsibilities (Expected Work): The RA Contractor is generally expected to be responsible for the following work activities: - Work independently to support the CPC, Research & Development Product Developers, Specification Management Team (SMT) and Material Expert Teams (MET) to review data and resolve differences that are compliant with global and local regulations. - Accountable for the review of data comparison information from our BPO. - Ensure all raw material data differences are properly documented. - Develop reports/trackers to summarize compare work findings. - Update data in specifications as needed. - Effectively communicate to members of CPC team and other functional groups as needed. Challenges: - Meeting critical deadlines by maintaining order and structure in a multi-tasked work flow. - Maintaining communications with CPC, BPO, Global METs, Regional METs, and other SMT team members in a manner that supports work flow and deadlines. - Learning new concepts quickly with minimal instruction to complete tasks. Position Requirements: - BS degree in science: Food Science, Biology, Chemistry or Nutrition preferred. - Must have strong organizational skills and be able to work well in a fast paced corporate environment, independently and as part of a team. - Ability to prioritize workload to meet strict project deadlines. - Strong written and verbal communication skills. - Maintain confidential information. - Must have basic knowledge of Microsoft Office (ability to create and maintain spreadsheets in MS Excel) - Knowledge of regulatory affairs / experience is FDA/USDA labeling regulations would be a distinct advantage. - Knowledge of SAP and/or other manufacturing systems a plus. Work hours Monday to Friday 8am-4pm If travel is required, is it Domestic or International? N/A Preferred interview method in-person Comments Entered Name Comment 01/29/2018 11:38 AM Cassandra Ashe While this role is classified under Spec Writer it is a bit different than former roles we have filled under this classification. However, this is a crucial role that works to support the Specification Management teams among other LOB. The individual will work to assist the Regulatory Affairs Manager and will be taking data extracted from systems to see where differences lie. They will be trained on the process but must be comfortable navigating various systems