Regulatory Specialist

Apolis; St. Louis (MO); On-site; USD 23,000 - 39,000; Full time

Job summary

Apolis is seeking a Regulatory Specialist to support R&D projects by guiding regulatory activities and coordinating import/export requirements for research samples. You will maintain regulatory plans, documentation, and compliance, partnering with R&D, Quality, Operations, Logistics, and external stakeholders.

The role involves developing regulatory plans, monitoring regulations, and ensuring proper recordkeeping. It is an onsite, 12-month+ contract in St.

Qualifications

• Bachelor’s degree in Life Sciences, Regulatory Affairs, Chemistry, Biology, or related field.
• Experience in regulatory, laboratory, pharmaceutical, biotech, or life sciences preferred.
• Knowledge of research sample import/export regulations preferred.
• Strong organization, communication, analytical, and problem-solving skills.
• Proficiency with documentation and standard business software.

Responsibilities

• Support regulatory requirements for R&D projects and sample shipments.
• Develop and maintain regulatory plans and documentation.
• Monitor applicable regulations and internal procedures.
• Coordinate import/export compliance for research samples.
• Identify and elevate regulatory risks or shipment issues.
• Partner with cross-functional teams to resolve compliance questions.
• Support process improvements and regulatory recordkeeping.

Skills

Organization

Communication

Analytical

Problem-solving

Education

Bachelor’s degree in Life Sciences, Regulatory Affairs, Chemistry, Biology, or related field

Tools

MS Office

Documentation software

Job description

Up to $28 per hour St. Louis, MO Onsite Job Classification: Professional Job Location: ONSHORE Estimated Project Duration: 12 months

Job Title- Regulatory Specialist
Location- St. Louis, MO 63102
Duration- 12 Month+ Contract

Job Summary: Support R&D projects by providing regulatory guidance and coordinating import/export requirements for research samples. Maintain regulatory plans, documentation, and compliance activities while partnering with R&D, Quality, Operations, Logistics, and external stakeholders.

Key Responsibilities:

• Support regulatory requirements for R&D projects and sample shipments.
• Develop and maintain regulatory plans and documentation.
• Monitor applicable regulations and internal procedures.
• Coordinate import/export compliance for research samples.
• Identify and elevate regulatory risks or shipment issues.
• Partner with cross-functional teams to resolve compliance questions.
• Support process improvements and regulatory recordkeeping.

Qualifications:

• Bachelor’s degree in Life Sciences, Regulatory Affairs, Chemistry, Biology, or related field.
• Experience in regulatory, laboratory, pharmaceutical, biotech, or life sciences preferred.
• Knowledge of research sample import/export regulations preferred.
• Strong organization, communication, analytical, and problem-solving skills.
• Proficiency with documentation and standard business software.