SonicJobs Logo
Left arrow iconBack to search

Sr. Compliance Specialist

Thermo Fisher Scientific
Posted 4 months ago, valid for 12 days
Location

St. Louis, MO, US

Salary

Competitive

Contract type

Full Time

By applying, a Sonicjobs account will be created for you. Sonicjobs's Privacy Policy and Terms & Conditions will apply.

SonicJobs' Terms & Conditions and Privacy Policy also apply.

Sonic Summary

info
  • The Senior Regulatory Compliance Specialist position requires an advanced degree with 6 years of experience or a bachelor's degree with 8 years of experience in compliance, quality systems, or regulatory affairs.
  • This role involves leading regulatory compliance activities, focusing on health authority and client audits, and ensuring adherence to Good Manufacturing Practices (GMP).
  • Key responsibilities include managing audit preparations, responses, and corrective actions, as well as collaborating with cross-functional teams to enhance compliance strategies.
  • Candidates should possess expertise in quality management systems, regulatory standards, and compliance management software, along with strong project management and analytical skills.
  • The salary for this position is competitive, though specific figures are not provided in the job description.

Work Schedule

Standard (Mon-Fri)

Environmental Conditions

Adherence to all Good Manufacturing Practices (GMP) Safety Standards, Cleanroom: no hair products, jewelry, makeup, nail polish, perfume, exposed piercings, facial hair etc... allowed, Office, Some degree of PPE (Personal Protective Equipment) required (safety glasses, gowning, gloves, lab coat, ear plugs etc.)

Job Description

The Senior Regulatory Compliance Specialist is responsible for leading and managing regulatory compliance activities with a strong focus on health authority and client audits. This role ensures that audit observations are effectively addressed, corrective and preventive actions (CAPAs) are robust and sustainable, and compliance with applicable regulations and standards is continuously maintained.

Key Responsibilities

Audit Management

  • Lead the planning, coordination, and execution of health authority inspections (e.g., FDA, EMA, MHRA) and client audits.
  • Serve as the primary point of contact during audits, ensuring timely and accurate communication with auditors.
  • Prepare audit-ready documentation and ensure site/functional readiness through routine assessments and mock audits.

Audit Response & Remediation

  • Oversee the review, classification, and response to audit observations, ensuring clarity, accuracy, and regulatory alignment.
  • Partner with cross-functional teams to develop comprehensive responses that address root causes.
  • Ensure timely submission of audit responses and commitments to regulatory authorities and clients.

CAPA Management & Effectiveness

  • Lead CAPA development, ensuring root cause analyses are thorough and scientifically sound.
  • Review and approve CAPA plans for adequacy, feasibility, and compliance risk mitigation.
  • Monitor CAPA implementation and verify effectiveness through appropriate metrics, trending, and follow-up activities.
  • Drive continuous improvement of CAPA processes to enhance compliance and operational performance.

Regulatory Compliance Oversight

  • Ensure ongoing compliance with applicable regulations (e.g., GMP, GLP, GCP as applicable) and internal quality systems.
  • Interpret regulatory requirements and translate them into actionable procedures and controls.
  • Support regulatory inspections and internal audits by providing subject matter expertise.

Cross-Functional Collaboration

  • Collaborate with Quality, Operations, Regulatory Affairs, and other stakeholders to ensure alignment on compliance strategies.
  • Provide guidance and training to teams on audit readiness, inspection conduct, and CAPA best practices.

Metrics & Reporting

  • Track, trend, and report audit findings, CAPA status, and compliance metrics to senior management.
  • Identify systemic issues and drive proactive improvements to reduce compliance risk.



REQUIREMENTS:
• Advanced Degree plus 6 years of experience, or Bachelor's Degree plus 8 years of experience in compliance, quality systems, or regulatory affairs
• Professional certifications in Quality Systems, Regulatory Compliance or others
• Expertise in quality management systems and regulatory standards (ISO, GMP, FDA)
• Experience with compliance management software (Veeva, MasterControl, trackwise)
• Proven ability to develop and implement standard operating procedures (SOPs)
• Strong project management and risk assessment capabilities
• Effective stakeholder management and cross-functional collaboration skills
• Advanced problem-solving and analytical skills
• Strong written and verbal communication abilities
• Demonstrated ability to lead internal/external audits
• Proficiency in Microsoft Office Suite and relevant compliance tools
• Strong attention to detail and ability to maintain accurate records
• Ability to work independently while contributing to team objectives
• Travel may be required




Learn more about this Employer on their Career Site

Apply now in a few quick clicks

By applying, a Sonicjobs account will be created for you. Sonicjobs's Privacy Policy and Terms & Conditions will apply.

SonicJobs' Terms & Conditions and Privacy Policy also apply.