Regulatory affairs specialist jobs in Union City, NJ

Job Details. Internal Job Title. Regulatory Affairs Associate II Duration. 12 months. Contract Location. Onsite. Clark, NJ Key Responsibilities Review formulas for compliance with local..

A company is looking for a Regulatory Affairs Specialist responsible for managing regulatory activities.. Key Responsibilities Provide strategic input on regulatory requirements for new technologies and product..

Responsibilities and Requirements. Support daily Regulatory Affairs function eg. compliance to 21 CFR.. Provides regulatory expertise in any significant or non significant changes. Support in maintaining and..

JOB SUMMARY. The Regulatory Affairs Manager will be responsible for independently compiling and.. from initial development to product termination, ensuring on time completion of regulatory milestone..

Our client is looking to fill the role of CMC Regulatory Affairs. This position will be hybrid and based.. Regulatory SOPs and reviewing and implementing policies and procedures. Required Qualifications..

Our client is seeking an experienced Regulatory Affairs professional to join their team based in North.. The Regulatory Affairs Manager will be responsible for ensuring compliance with all regulatory standards..

Innovating every day. The Senior Director, Regulatory Affairs will lead and formulate the regulatory.. Supervise 3 regulatory affairs specialists. Position Requirements Must have a master's degree in..

Months with the possibility of extension Intake Call Notes. This is an entry level position within R&I. It is not a lab based role, but rather a corporate 'desk job' supporting regulatory..

We are proud to offer an opportunity to work as a Sr Scientist, Regulatory Affairs located in Clark, NJ.. 0 60 hr Purpose of the Role. Administer regulatory affairs over the product lifecycle from pre market..

FDA EMA) guidelines for NDA MAA IND or CTA interactions. Manage the regulatory activities for multiple.. Support the development of regulatory strategy and update strategy based upon regulatory changes..

I look forward to hearing from you soon Job. 36317 Job Title. Global Regulatory Affairs Documentation Specialist Location. Rahway, NJ Duration. 12 months contract (Potential to extend) Benefits..

We are proud to offer an opportunity to work as a Sr Scientist, Regulatory Affairs located in Clark, NJ.. 0 60 hr Purpose of the Role. Administer regulatory affairs over the product lifecycle from pre market..

Description templates and other group health plan documents.Perform additional tasks and lead additional work streams, from time to time and upon request, concerning the regulatory regime or..

On Board Scientific is hiring a Regulatory Affairs Assistant!For immediate consideration please send.. st shiftBenefits Compensation. per hour based on previous experience The Regulatory Assistant needs to..

Product Stewardship Specialist Lyndhurst, NJ, USA Company Description With over 100 years of experience.. Job Description Product Regulatory expert for Construction Chemical Company responsible for preparing..

Job Description. POSITION Nonclinical Regulatory Document and Scientific Writer DEPARTMENT Nonclinical.. Regulatory submissions will span across all therapeutic areas (cancer, immunology, neurology etc..

Our client is looking to fill the role of CMC Regulatory Affairs. This position will be hybrid and based.. Bachelor's degree in science Minimum 5 years of Regulatory Affairs experience in the industry SAP and..

Job Description The Director Regulatory Affairs, Strategic Labeling is responsible for setting strategy.. Establishes labeling policy compliant with changing regulatory environment. Manages labeling staff for..