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Specialist, Regulatory Affairs

Job in Lincoln, Lancaster County, Nebraska, 68511, USA
Listing for: Allergan
Full Time position
Listed on 2026-03-04
Job specializations:
  • Healthcare
    Healthcare Compliance
Salary/Wage Range or Industry Benchmark: 60000 - 80000 USD Yearly USD 60000.00 80000.00 YEAR
Job Description & How to Apply Below

Job Description

Coordinate, prepare, or review regulatory submissions for domestic or international projects.

Responsibilities
  • Provide technical review of data or reports that will be incorporated into regulatory submissions to assure scientific rigor, accuracy, and clarity of presentation.
  • Review product promotional materials, labeling, batch records, specification sheets, or test methods for compliance with applicable regulations and policies.
  • Maintain current knowledge base of existing and emerging regulations, standards, or guidance documents.
  • Interpret regulatory rules or rule changes and ensure that they are communicated through corporate policies and procedures.
  • Determine the types of regulatory submissions or internal documentation that are required in situations such as proposed device changes or labeling changes.
  • Advise project teams on subjects such as premarket regulatory requirements, export and labeling requirements, or clinical study compliance issues.
  • Prepare or maintain technical files as necessary to obtain and sustain product approval.
  • Coordinate efforts associated with the preparation of regulatory documents or submissions.
  • Prepare or direct the preparation of additional information or responses as requested by regulatory agencies.
Qualifications
  • 3 year working experience with a minimum of 2 years experience required in Regulatory, R&D or related area
  • Minimum of 1 years experience preferred in pharmaceutical regulatory affairs.
  • Having experience interfacing with government regulatory agencies and proven skill at developing and implementing successful China regulatory strategies.
  • Biologics experience a plus. Experience in Gastro, Liver, CV, Urology, CNS, Vaccine, etc. is a plus
  • Fluent English both oral and written
  • Working Computer Operation skill
  • Is willing to travel
  • Experience working in a complex and matrixed environment is required. Dependent on individual aptitude
  • Up to date knowledge of legislation
  • Self motivated
Additional Information

Abb Vie is an equal opportunity employer and is committed to operating with integrity, driving innovation, transforming lives and serving our community. Equal Opportunity Employer/Veterans/Disabled.

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