Regulatory Affairs Specialist

Yoh
Maryland Heights, MO, US
$34 an hour
Full-time

Yoh is seeking a Regulatory Affairs Specialist for our Pharmaceutical client here in St. Louis, Missouri. Join a growing team!

Position Type : Contract (Hybrid)

Rate : $30-$34 / hr

Hours : 8 : 00 am - 5 : 00 pm

Position Summary :

  • Plan / author / compile drug product dossiers in CTD format for expansion to international markets
  • Plan / author / compile / submit / manage variations for marketed products outside the United States Respond to health authority information requests and comments to achieve approval Review and assess CMC regulatory impact and provide regulatory strategy for post-approval changes proposed at the manufacturing site
  • Participate in cross-functional teams and provide health authority requirements needed for support of initial international filings and post-approval changes Facilitate the creation of foreign language labeling content to meet local health authority requirements
  • Maintain regulatory knowledge of current guidelines and regulations.
  • Maintain current regulatory databases and produce various reports as needed.

Essential Functions

  • Authoring, organization, and preparation of CTD regulatory filings; also includes peer review of filings.
  • Understand, identify potential regulatory risks and recommend strategies based on current ICH and health authority requirements
  • Manage multiple priorities Attend necessary trainings and seminars to keep abreast of new and / or changes in the Regulatory profession.

Process, interpret, and provide recommendations for complex, unusual issues.

Critically review documentation for regulatory submissions and provide input for necessary revisions.

Requirements (Education)

  • Bachelor Degree in scientific discipline required or equivalent work experience. 3 or more years of Regulatory experience or related field required.
  • Self-starter who takes initiative to learn, grow and excel as a Regulatory Affairs professional.
  • Background in manufacturing, research and development, or quality assurance sufficient to understand how products are produced and marketed.
  • Strong organizational skills, strong attention to detail, ability to problem solve and to work well with others and cross-functionally.
  • Cross-functional interaction experience, coordinating activities, driving assigned submissions to completion, and working to align communications with other departments is required.

Estimated Min Rate

$30.00

Estimated Max Rate

$34.00

Note : Any pay ranges displayed are estimations. Actual pay is determined by an applicant's experience, technical expertise, and other qualifications as listed in the job description.

All qualified applicants are welcome to apply.

Yoh, a Day & Zimmermann company, is an Equal Opportunity Employer. All qualified applicants will receive consideration for employment without regard to race, color, religion, sex, sexual orientation, gender identity, national origin, disability, or status as a protected veteran.

Visit

https : / / www.yoh.com / applicants-with-disabilities

to contact us if you are an individual with a disability and require accommodation in the application process.

For California applicants, qualified applicants with arrest or conviction records will be considered for employment in accordance with the Los Angeles County Fair Chance Ordinance for Employers and the California Fair Chance Act.

All of the material job duties described in this posting are job duties for which a criminal history may have a direct, adverse, and negative relationship potentially resulting in the withdrawal of a conditional offer of employment.

12 days ago
Related jobs
Promoted
VirtualVocations
Saint Charles, Missouri

A company is looking for a Principal Regulatory Affairs Specialist, US Regulatory Policy. FDA regulatory requirements and policyRegulatory experience within the medical device industry or a regulatory agencyExperience in advocacy related to healthcare policy and regulationsStrong research and analyt...

Promoted
Yoh
Maryland Heights, Missouri

Yoh is seeking a Regulatory Affairs Specialist for our Pharmaceutical client here in St. Plan/author/compile/submit/manage variations for marketed products outside the United States Respond to health authority information requests and comments to achieve approval Review and assess CMC regulatory imp...

Promoted
VirtualVocations
Saint Charles, Missouri

A company is looking for a Regulatory Affairs Specialist I to manage regulatory documentation and submissions. ...

Promoted
Yoh
St. Louis, Missouri

Regulatory Affairs Specialist . Review and assess CMC regulatory impact and provide regulatory strategy for post-approval changes proposed at the manufacturing site. Self-starter who takes initiative to learn, grow and excel as a Regulatory Affairs professional. This individual will need to have a s...

Curium Live Forward
St. Louis, Missouri

The (Contractor) Regulatory Affairs Specialist responsibilities encompass the support of international drug product applications. Review and assess CMC regulatory impact and provide regulatory strategy for post-approval changes proposed at the manufacturing site. Self-starter who takes initiative to...

Beacon Hill
Maryland Heights, Missouri

The Regulatory Affairs Specialist responsibilities encompass the support of international drug product applications. Review and assess CMC regulatory impact and provide regulatory strategy for post-approval changes proposed at the manufacturing site. Self-starter who takes initiative to learn, grow ...

STERIS
St. Louis, Missouri

Manager, Regulatory Affairs and other Regulatory Affairs staff with all regulatory matters. Reporting to the Manager, Regulatory Affairs within the RA Department, the incumbent is responsible for supporting the development and administration of STERIS’s global regulatory responsibilities. Regulatory...

Spectrum Brands
Earth City, Missouri

As the Senior Regulatory Specialist, you will work with cross functional teams, providing guidance and direction to ensure regulatory compliance across the organization. The Senior Regulatory Specialistutilizes people skills, regulatory knowledge and experience gained to support internal cross-funct...

Yoh, A Day & Zimmermann Company
St. Louis, Missouri

Regulatory Affairs Specialist . Review and assess CMC regulatory impact and provide regulatory strategy for post-approval changes proposed at the manufacturing site. Self-starter who takes initiative to learn, grow and excel as a Regulatory Affairs professional. This individual will need to have a s...

Yoh, A Day & Zimmermann Company
Maryland Heights, Missouri

Yoh is seeking a Regulatory Affairs Specialist for our Pharmaceutical client here in St. Plan/author/compile/submit/manage variations for marketed products outside the United States Respond to health authority information requests and comments to achieve approval Review and assess CMC regulatory imp...