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USA_Regulatory Associate - Level 3

Lancesoft
  • Warren, NJ
  • Instant Apply
30+ days ago

Job Description

Title: Regulatory Associate
Pay Rate $47.00 49.15/hr on W2
Location:Warren, NJ 07059
Duration: 12 Months
Day Shift: 8 am - 5 PM


Job Description:
Regulatory Affairs Senior Associate
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 Client/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

Numbers & Facts

LocationWarren, NJ
IndustryStaffing/Employment Agencies
Company Size2,000 to 2,499 employees
Year Founded2000
Websitehttp://www.lancesoft.com/

About Company

We are a $125 Million, NMSDC-certified Minority & Woman owned Workforce Solutions Company headquartered in the DC metro area with presence across US with global presence - Canada, Mexico, India, UK, Malaysia, Indonasia, Hongkong, Singapore, UAE. We are specialized in providing Workforce Solutions, SOW project delivery, Engineering Solutions, Creative Services. We currently support 100+ Fortune companies globally and across multiple industry segments. We are currently supporting several massive programs across industry segment nationally/globally (Intel, Ally, AMD, QUALCOMM, Morgan Stanley, Kraft/ Mondelez, MNP, Amdocs, Dell, SanDisk, Medtronic, Becton Dickinson, GE, Lockheed Martin, UTC, L-3 Communications, Caterpillar, BMW, Mercedes Benz, National Grid, Dominion, Energy Future Holdings, PSEG, 3M, Fidelity, Aetna, Humana, Johnson & Johnson, Pfizer, Merck etc). 

All qualified applicants will receive consideration for employment without regard to race, color, religion, sex, sexual orientation, gender, identity, national origin, disability, or protected veteran status.

Skills

  • Agile Programming Methodologiesunmatched
  • Biologyunmatched
  • Biotech and Pharmaceuticalunmatched
  • Chemistryunmatched
  • Communication Skillsunmatched
  • Cross-Functionalunmatched
  • Detail Orientedunmatched
  • Establish Prioritiesunmatched
  • FDA (Food and Drug Administration)unmatched
  • FDA Requirementsunmatched
  • Healthcareunmatched
  • Leadershipunmatched
  • Maintain Complianceunmatched
  • Manufacturingunmatched
  • Medical Equipmentunmatched
  • People Managementunmatched
  • Performance Metricsunmatched
  • Presentation/Verbal Skillsunmatched
  • Process Improvementunmatched
  • Product Developmentunmatched
  • Product Documentationunmatched
  • Product Lifecycleunmatched
  • Product Reviewsunmatched
  • Product/Service Launchunmatched
  • Project/Program Managementunmatched
  • Regulationsunmatched
  • Regulatory Complianceunmatched
  • Regulatory Requirementsunmatched
  • Riskunmatched
  • Strategic Planningunmatched
  • Systems Maintenanceunmatched
  • Team Playerunmatched
  • Time Managementunmatched
  • Writing Skillsunmatched

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