ZipRecruiter

Log In

2

Remote Inventory Control Specialist Jobs in Riverside, CA

JenaValve

Senior Manager, Clinical Compliance

Irvine, CA · On-site +1

$160K - $170K/yr

Remote - Home Office Summary: Reporting to the Vice President, Clinical Affairs, the Senior Manager ... This individual directly manages the Specialist, Clinical Compliance. Job Responsibilities:

New

Saratech

CAM Technical Manager

Mission Viejo, CA · Remote

$60 - $65/hr

The CTM needs to be a highly skilled engineering specialist with strong skills in mechanical ... This is a full-time remote position. Ideal candidates will possess the following qualifications ...

Henry Schein, Inc.

Manager, Accounting

Placentia, CA · On-site +1

$110.69K - $152.20K/yr

... inventory cost accounting is compliant with US GAAP. This position will manage a hybrid / remote ... Responsible for maintaining an effective internal control structure along with compliance with SOX, ...

Henry Schein

Manager, Accounting

Placentia, CA · On-site +1

$110.69K - $152.20K/yr

... inventory cost accounting is compliant with US GAAP. This position will manage a hybrid / remote ... Responsible for maintaining an effective internal control structure along with compliance with SOX, ...

ABB

Strategic KAM - eOEM

La Verne, CA · Remote

... specialists within scope) to achieve the sales targets, through high performance ... While this is a remote position, successful candidates should be located in a major metro area in ...

New

ABB

Strategic KAM - eOEM

Irvine, CA · Remote

... specialists within scope) to achieve the sales targets, through high performance ... While this is a remote position, successful candidates should be located in a major metro area in ...

New

next page

Showing results 1-20

People also search for

All JobsRemote Inventory Control Specialist JobsRemote Inventory Control Specialist Jobs in Riverside, CA

Remote Inventory Control Specialist information

See Riverside, CA salary details

$13

$21

$30

How much do remote inventory control specialist jobs pay per hour?

As of May 31, 2026, the average hourly pay for remote inventory control specialist in Riverside, CA is $21.39, according to ZipRecruiter salary data. Most workers in this role earn between $18.08 and $23.32 per hour, depending on experience, location, and employer.

What is the difference between Remote Inventory Control Specialist vs Remote Warehouse Associate?

AspectRemote Inventory Control SpecialistRemote Warehouse Associate
CredentialsInventory management certifications, ERP system knowledgeLogistics or warehouse operation certifications
Work EnvironmentOffice or remote, focused on data and system managementRemote or on-site, involved in physical or virtual warehouse tasks
Industry UsageRetail, manufacturing, distribution companiesLogistics, supply chain, e-commerce warehouses
Search/Comparison IntentManaging inventory levels remotely, system oversightHandling warehouse operations remotely or on-site

The Remote Inventory Control Specialist primarily manages inventory data, oversees stock levels, and uses ERP systems remotely. In contrast, the Remote Warehouse Associate focuses on warehouse operations, including stock handling and order fulfillment, either remotely or on-site. Both roles are essential in supply chain management but differ in their focus and daily tasks.

What are the most commonly searched types of Inventory Control Specialist jobs in Riverside, CA? The most popular types of Inventory Control Specialist jobs in Riverside, CA are:
What are popular job titles related to Remote Inventory Control Specialist jobs in Riverside, CA? For Remote Inventory Control Specialist jobs in Riverside, CA, the most frequently searched job titles are:
What job categories do people searching Remote Inventory Control Specialist jobs in Riverside, CA look for? The top searched job categories for Remote Inventory Control Specialist jobs in Riverside, CA are:
What cities near Riverside, CA are hiring for Remote Inventory Control Specialist jobs? Cities near Riverside, CA with the most Remote Inventory Control Specialist job openings:
Remote Inventory Control Specialist jobs near you
Infographic showing various Remote Inventory Control Specialist job openings in Riverside, CA as of May 2026, with employment types broken down into 1% As Needed, 62% Full Time, 32% Part Time, 1% Temporary, 3% Contract, and 1% Nights. Highlights an 96% Physical, 2% Hybrid, and 2% Remote job distribution, with an average salary of $44,483 per year, or $21.4 per hour.
Senior Manager, Clinical Compliance

Senior Manager, Clinical Compliance

JenaValve

Irvine, CA • On-site, Remote

$160K - $170K/yr

Full-time

Posted 2 days ago

Job description

Job Title: Senior Manager, Clinical Compliance
Role Level: People Manager
Supervisor/Manager Title: VP, Clinical Affairs
Job Location & Environment: Remote - Home Office
Job Description Summary: Reporting to the Vice President, Clinical Affairs, the Senior Manager, Clinical Compliance owns the clinical compliance program for JenaValve's active clinical studies. This includes the audit program (internal and investigational site), vendor qualification and quality oversight, department procedure lifecycle, regulatory intelligence, and internal training. The role works in close partnership with the Quality organization to ensure alignment on quality systems, audit scheduling and conduct, and CAPA processes, and serves as the primary compliance bridge between Clinical Affairs and Quality. This individual directly manages the Specialist, Clinical Compliance.
Job Responsibilities:
  • Develop and execute a risk-based audit program covering internal processes and investigational sites; author audit plans and reports, and lead inspection readiness activities including TMF health assessments and mock inspections; partner with Quality on audit scheduling, joint audit conduct, and preparation for regulatory agency inspections (FDA, EU Notified Body) and corporate quality audits.
  • Own CAPA and non-conformance management for the department; serve as the central accountability point for CAPA status, effectiveness checks, and closure, coordinating with functional owners across sub-teams; maintain alignment with Quality on CAPA creation, classification, and tracking to ensure consistency with enterprise quality system requirements.
  • Own the vendor qualification and ongoing quality oversight program for CROs, core labs, EDC vendors, and other clinical service providers; issue and track SCARs, evaluate corrective action responses, and escalate unresolved quality issues with contract implications to leadership.
  • Lead the Clinical Affairs procedure lifecycle, including authoring, reviewing, and approving SOPs and work instructions; coordinate the annual review cycle across sub-departments; maintain the controlled document management system in alignment with enterprise quality system standards, serving as the primary liaison to Quality on document control processes and procedure governance.
  • Monitor and communicate regulatory developments and GCP guidance updates (FDA, ICH, EU CTR); evaluate impact on operations and procedures and serve as the department's internal GCP compliance subject matter expert.
  • Design and deliver the Clinical Affairs internal training program, including GCP onboarding, procedural updates, and audit corrective action training; maintain training matrices and completion records for all department personnel.
  • Directly manage and develop the Specialist, Clinical Compliance; provide day-to-day direction, performance feedback, and professional development support.
  • Support continuous process improvement and PMA/IDE activities as they relate to compliance, study conduct quality, and regulatory commitments; complete training for internal SOPs and maintain current regulatory knowledge.

Required Education and Experience:
  • 7+ years in clinical research, clinical operations, or clinical quality assurance; medical device experience strongly preferred.
  • Minimum 3 years dedicated GCP audit or clinical compliance experience; demonstrated experience as a lead auditor conducting both site and vendor/CRO audits required.
  • Bachelor's degree or higher in life sciences, health sciences, or a related field required; advanced degree preferred.
  • Thorough knowledge of ICH E6(R3), FDA regulations (21 CFR Parts 11, 50, 54, 56, 812), and ISO 14155; demonstrated SOP authorship and procedure lifecycle management experience.
  • Prior people management experience; ability to lead and develop direct reports in a fast-paced, growing organization.
  • Cardiovascular or structural heart therapeutic area experience is a significant advantage.

Skills and Abilities Required for This Job:
  • Lead auditor competency (planning, execution, report writing, finding classification); lead auditor certification (ASQ, RAPS, or equivalent) preferred.
  • Experience with CAPA programs and risk-based quality management (RBQM); strong analytical and root cause analysis skills.
  • Ability to influence without direct authority across clinical operations, data management, biostatistics, regulatory affairs, and medical affairs; proven cross-functional credibility.
  • Excellent written and oral communication skills; able to produce clear audit reports, procedure documents, and executive compliance summaries; proficient in Microsoft Office Suite and eTMF/document management systems.

Physical Requirements:
  • Standard office environment requirements.
  • Travel up to 25%, primarily for investigational site audits, vendor audits, clinical meetings, and periodic home office visits.

Apply