Job Title: Regulatory Affairs Senior Associate
Location: Warren, NJ 07059 (HYBRID, Onsite or 3 days in office)
Duration: 6 Months (Possibility of extension depending upon business requirements and performance)
Shift: 8-5
 
Description:

• The purpose of this role is to execute OTC regulatory activities for new products registrations and life-cycle maintenance for the portfolio of products defined by the US Business Units.

 
Key Responsibilities:
These responsibilities include some of the following.

• Represent USRA on assigned projects, provide guidance on OTC drug regulatory pathways (monograph, NDA).
• Develop regulatory strategies and documents for new product launches and maintenance of current products aligned with the regulations
• Develop regulatory label for OTC products, review claims and copy
• Participate in the review of promotional materials
• Support end-to-end regulatory compliance of products in remit.
• Applies system and procedure updates to maintain up to date technical product records
• Identifies and participates in process improvements within US Regulatory Affairs
• Interact with colleagues in other global functions to support global programs
• Effectively communicates regulatory technical requirements and guidelines, facilitating timely and complete submissions
• Develop up-to-date knowledge of guidelines and regulatory requirements, as well as technical trends

 
Qualifications:

• Bachelor’s degree in Pharmaceutical or Life Sciences or equivalent regulatory experience
• 2-4 years’ experience in regulatory affairs including chemistry, manufacturing and controls, and over the
• counter experience, preferably within a CPG/Consumer Healthcare/Pharma related industry.
• Experience and knowledge in Quality, product development and manufacturing areas.
• Experience working on FDA applications, OTC monograph products, chemistry, manufacturing and controls
• Proficient knowledge in US FDA regulations
• Regulatory Affairs Senior Associate
• Excellent communications skills, stakeholder management and enjoys working in multidisciplinary teams
• Ability to manage prioritize projects of high complexity
• Experience leading end-to-end regulatory process in new product launches

 
Additional Preferred Qualifications:

• Knowledge and experience of US regulatory framework for OTC drugs, OTC medical devices
• Ability to ensure compliance standards and key performance indicators are met
• Regulatory expertise in knowledge of the regulatory lifecycle
• Ability to interact at many levels
• Technical knowledge
• Minimum 2 years of experience in regulatory affairs

 
Competencies and Skills:

• Agile, attention to detail, written and verbal communication skills– using evidence and applying judgement to balance pace, rigor and risk

 
 
At SPECTRAFORCE, we are committed to maintaining a workplace that ensures fair compensation and wage transparency in adherence with all applicable state and local laws. This position’s starting pay is: $ 49.00/hr.