Compliance Manager at Overnight Freight inc
Stockton, CA 95205, USA -
Full Time


Start Date

Immediate

Expiry Date

08 Nov, 25

Salary

0.0

Posted On

08 Aug, 25

Experience

0 year(s) or above

Remote Job

Yes

Telecommute

Yes

Sponsor Visa

No

Skills

Chemistry, Project Management Skills, Compliance Management, Life Sciences, Communication Skills

Industry

Pharmaceuticals

Description

JOB SUMMARY

We are seeking a dedicated and detail-oriented Compliance Manager to oversee and ensure adherence to regulatory standards within our organization. The ideal candidate will possess a strong background in chemistry, manufacturing, and controls, with a thorough understanding of FDA regulations and compliance management. This role is crucial in maintaining the integrity of our clinical trials and ensuring that all processes meet quality assurance standards.

EXPERIENCE

  • Bachelor’s degree in a relevant field such as Chemistry, Life Sciences, or related discipline; advanced degree preferred.
  • Proven experience in compliance management within the pharmaceutical or biotechnology industries.
  • Strong knowledge of FDA regulations, clinical trial processes, and quality assurance principles.
  • Demonstrated project management skills with the ability to lead cross-functional teams effectively.
  • Excellent research skills with a keen attention to detail.
  • Strong communication skills, both written and verbal, with the ability to convey complex information clearly. Join our team as a Compliance Manager where you can make a significant impact on our operations while ensuring that we uphold the highest standards of quality and regulatory adherence.
    Job Types: Full-time, Part-time, Contract, Temporary
    Pay: $11.00 - $25.00 per hour
    Expected hours: 20 – 40 per week

Benefits:

  • Relocation assistance

Ability to Commute:

  • Stockton, CA 95205 (Required)

Ability to Relocate:

  • Stockton, CA 95205: Relocate before starting work (Required)

Work Location: In perso

How To Apply:

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Responsibilities
  • Develop, implement, and manage compliance programs to ensure adherence to FDA regulations and industry standards.
  • Oversee the compliance aspects of clinical trials, ensuring all research activities comply with applicable laws and guidelines.
  • Conduct regular audits and assessments to identify areas for improvement in compliance practices.
  • Collaborate with cross-functional teams to promote a culture of compliance throughout the organization.
  • Provide training and guidance on compliance-related issues to staff at all levels.
  • Monitor changes in regulatory requirements and update policies and procedures accordingly.
  • Prepare reports on compliance activities for senior management and regulatory bodies.
  • Manage projects related to compliance initiatives, ensuring timely completion and alignment with organizational goals.
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