Compliance Associate - San Diego

The company is seeking a Compliance Associate to support their Annual Compliance Review and test compliance procedures associated with investment guidelines and restrictions mandated by the Adviser's clients and applicable rules/regulations for multiple internal departments/busin ...

We are PCI. Our investment is in People who make an impact, drive progress and create a better tomorrow. · Life changing therapies. Global impact. Bridge to thousands of biopharma companies and their patients.This position has the utmost responsibility for compliance with the rul ...

We are PCI.Our investment is in People who make an impact · , drive progress and create a better tomorrow. · The Sr. Compliance Associate I will utilize their skills to hosts customer · and regulatory audits, assist in the execution of internal audits, and provide support to the ...

Under the direction of the Manager, Quality & Regulatory Affairs, the Quality Assurance and Compliance Specialist II participates in maintaining a Quality Management System that supports the manufacture of FDA-regulated biologic blood, cell and tissue products and other related r ...

+Capricor Therapeutics is a biotechnology company seeking an individual to join their Quality Compliance department. The ideal candidate will conduct internal and external audits to ensure compliance with applicable regulations and standards. · +Responsibilities include planning, ...

We are seeking an individual to join our Quality Compliance department. This role conducts internal and external audits to ensure our biopharma operations comply with applicable regulations, standards, and company procedures.,Responsibilities: Plan conduct report riskbased GxP au ...

We are seeking an individual to join our Quality Compliance department. This role conducts internal and external audits to ensure our biopharma operations comply with applicable regulations, standards, and company procedures. · ...

We are seeking an individual to join our Quality Compliance department. This role conducts internal and external audits to ensure our biopharma operations comply with applicable regulations, · Plan, conduct and report risk-based GxP audits across manufacturing. · Lead and support ...

The Quality Assurance and Compliance Specialist II participates in maintaining a Quality Management System that supports the manufacture of FDA-regulated biologic blood, cell and tissue products. · ...

The Associate Director leads quality assurance activities to protect data integrity and regulatory readiness across Acadia Pharmaceuticals' nonclinical and clinical portfolio. ...

+Job summary: · About Acadia Pharmaceuticals · Acadia is committed to turning scientific promise into meaningful innovation that makes the difference for underserved neurological and rare disease communities around the world.+ · +Plan schedule coordinate conduct internal external ...

The Associate Director plays a critical role in protecting data integrity and regulatory readiness across the company's nonclinical and clinical portfolio. · Plan, schedule, coordinate, and conduct internal and external GLP/GCP audits of company functions and Contract Service Pro ...

The Business and Workforce Compliance Division ensures that SANDAG activities comply with all applicable federal,state,and local requirements related to Business and Workforce Compliance, · This position will collaborate with internal and external stakeholders to maximize opportu ...

Associates in Store Support positions are responsible for a variety of non-sales functions. This may include ensuring an outstanding customer order fulfillment experience. · ...

The Store Support position is responsible for various non-sales functions including customer order fulfillment and administrative services. · Ensure an outstanding customer order fulfillment experience. · Assist customers in the lot or provide administrative services. · ...

We are seeking a Regulatory Affairs Associate II with hands-on medical device regulatory experience to support U.S. and global submissions. · Prepare and manage U.S. and global regulatory submissions (FDA, EU MDR) · Support change assessments and regulatory impact analyses ...

This position provides support and coordination of critical quality and compliance systems for Global Operations R&D California. · Responsible and accountable for a wide range of tasks attributable to quality systems and other Global Operations compliance systems. · ...

We are seeking a Regulatory Affairs Associate to support U.S. and global regulatory submissions for medical device products. · Bachelor's Degree required, preferably in pharmacy, biology, chemistry, pharmacology, engineering or related subject. · 2–4 years of Regulatory Affairs e ...

The Associate Director/Director Drug Safety & Pharmacovigilance Quality & Compliance would report directly into the Chief Safety Officer and have a team below them. · This leader is responsible for overseeing PV quality systems compliance oversight and alliance management while m ...