Regulatory Affairs Rotational Program — Medical Devices

Abbott; Santa Clara (CA); On-site; USD 70,000 - 90,000; Full time

Benefits offered by this job

Free medical coverage in HIP PPO plan

Excellent retirement plan with high-em

Tuition reimbursement

FreeU education benefit

Recognized as a great place to work

Job summary

Abbott is seeking candidates for the Medical Device Regulatory Affairs Development (RAD) Program with rotations in Alameda, Pleasanton, Santa Clara, CA, Minneapolis, MN or Plano, TX. The program provides three 1-year rotations, with responsibilities spanning regulatory submissions, documentation preparation, and support for global regulatory operations.

Ideal candidates have a life sciences or engineering background, strong communication skills, and the ability to adapt in a matrixed, fast-paced

Qualifications

• Ability to work in a highly matrixed and geographically diverse business environment.
• Strong verbal and written communication across multiple levels.
• Domestic travel to various US locations based on rotational assignment.

Responsibilities

• Assists in the preparation of regulatory applications (including annual reports) to achieve departmental and organizational objectives.
• Creates, reviews and approves engineering changes.
• Acts as a regulatory representative responsible for review and analysis of applicable regulatory guidelines.
• Reviews protocols and reports to support regulatory submissions.
• Supports all Company initiatives as identified by management and in support of QMS/EMS and other regulatory requirements.

Skills

Regulatory knowledge

Verbal and written communication

Team collaboration

Attention to detail

Multitasking

Regular attendance

Mobility to US locations

Education

BA/BS in life sciences or engineering

Tools

Regulatory database

SharePoint

Job description

Abbott is seeking candidates for the Medical Device Regulatory Affairs Development (RAD) Program with rotations in Alameda, Pleasanton, Santa Clara, CA, Minneapolis, MN or Plano, TX. The program provides three 1-year rotations, with responsibilities spanning regulatory submissions, documentation preparation, and support for global regulatory operations.

Ideal candidates have a life sciences or engineering background, strong communication skills, and the ability to adapt in a matrixed, fast-paced