Company Description

eTeam was formed in 1999 with the goal of becoming the supplier of choice for clients, employees and contingent workers. Today, we’re one of the fastest-growing companies in New Jersey and ranked as one of the best companies to work for by Staffing Industry Analysts and New Jersey Business. We’re also an honored member of Deloitte’s Technology Fast 50

Job Description

Develop regulatory submissions and assessments (in compliance with applicable regulations and standards) to ensure timely global commercialization of products.
ESSENTIAL DUTIES AND RESPONSIBILITIES
With moderate supervision, responsible for the following Regulatory activities:
• Develop and implement regulatory strategies and processes to ensure timely global commercialization of products in compliance with applicable regulations and standards.
• Author regulatory submissions and assessments for class II and III medical devices to be distributed in the US to ensure timely global commercialization of products in compliance with applicable regulations and standards.
• Author technical files and design dossiers for products to be distributed in the EU.
• Prepare international documentation to support product registration internationally.
• Directly communicate with FDA and other Regulatory agencies in preparing responses to submissions and in support of agency audits.
• Evaluate proposed changes to product design or manufacturing processes and assess impact of the proposed changes with regard to worldwide approvals and internal BWI policies and procedures.
• Participate on new product development teams.
• Review and approve new product development and product modification documentation.
• Write, review and revise company SOPs as required.
• Communicate business related issues or opportunities to next management level.
• Ensure personal and Company compliance with all Federal, State, local and Company regulations, policies, and procedures.
• Perform other duties assigned as needed.

Qualifications

• BS degree in Engineering, Physical or Biological science a minimum of 4 - 6 years experience in Regulatory experience or advanced degree 2 - 4 years experience in Regulatory Affairs.

REQUIRED KNOWLEDGE, SKILLS, ABILITIES and CERTIFICATIONS/LICENSES:
• Must be familiar with MS Office applications
• Excellent communication skills (verbal and written)
• Project management skills
• Problem solving skills
• Presentation skills
• RAC Certification preferred

Additional Information

Thanks & Regards

Neha Sharma

Lead Recruiter

eTeam Inc – “ACCELERATED HIRES”

Efficiency, Synergy, Expertise

T-732-248-1900 .Ext 120

Awards

#1 Best Places to work in New Jersey-2009,2008,2007,2006

Top Small Diversity Business, 2006 by DiversityBusiness.com

Deloitte Technology Fast 500-2007,2006

IMPORTANT NOTE: Under Bills.1618 Title III passed by the 105th U.S. Congress, this email cannot be considered spam as long as it contains our contact information and a link for the removal requests. If you have received this mail in error or prefer not to receive such emails in the future, please reply with "REMOVE" in the subject line and the email id(s) to be removed. All removal requests will be honored ASAP. We sincerely apologize for any inconvenience caused.