Top 62 Associate manager Jobs in Poway Ca

Associate Regulatory Affairs Manager (San Diego) - Bilingual (Mandarin Speaking)
CorDx —San Diego, CA
- $80,000 - $120,000 a year
- Full-time
- Mid-level
- Office
- Mentoring
- Health insurance
- Dental insurance
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Executive Recruiting - Sourcing Associate Manager
Accenture —San Diego, CA
- $68,300 - $218,800 a year
- Full-time
- Mid-level
- US work authorization
- Military encouraged
- Paid holidays
- Disability insurance
5d
Associate Field Services Technology Manager
Hilton —San Diego, CA
- $67,500 - $95,000 a year
- Weekends as needed
- Mid-level
- Hotel
- High school diploma or GED
- Paid parental leave
- Employee stock purchase plan
3d
Associate Store Manager
J.Crew Factory —San Marcos, CA
- Weekends as needed
- Sales
- Merchandising
- Mid-level
- Paid holidays
- Health insurance
3d
Manager/ QA Associate, GxP Quality Systems
Ionis Pharmaceuticals, Inc. —Carlsbad, CA
- $70,844 - $102,371 a year
- Hybrid work
- Data analysis skills
- Mid-level
- 3 years
Quick Apply
4d
Oracle ICM Configuration Lead - Associate Manager
Accenture —San Diego, CA
- $68,300 - $218,800 a year
- Full-time
- Oracle
- ERP systems
- Mid-level
- Paid holidays
- Disability insurance
4d

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Associate Regional Operations Manager SNF Dialysis
DAVITA —Canal Winchester, OH
We are proud to be an equal opportunity workplace and comply with state and federal affirmative action requirements. DaVita is a clinical leader!
Executive Recruiting - Sourcing Associate Manager
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associate manager jobs near poway ca

Associate Regulatory Affairs Manager (San Diego) - Bilingual (Mandarin Speaking)

CorDx -
San Diego, CA

Quick Apply

Job Details

Full-time
$80,000 - $120,000 a year

Benefits

Health insurance
Dental insurance
401(k)
Paid time off
Vision insurance

Qualifications

FDA submissions
Records management
Project management experience in healthcare
Regulatory submission editing and review
Managing projects
Productivity software
Document management systems
Cross-functional communication

Full Job Description

Who is CorDx？

CorDx a multi-national biotech organization focused on pushing the limits of innovation and supply in global health. With over 2,100 employees across the world, serving millions of users in over 100 countries, CorDx delivers rapid testing and point-of-care medical device solutions used in the detection of infectious disease such as COVID-19, pregnancy, drugs of abuse, biomarkers, and more. CorDx is at the cutting edge of technology, artificial intelligence, and data science with the goal of delivering diagnostic solutions to some of the most critical questions in healthcare.

Job Type: Full time
Job Title: Associate Regulatory Affairs Manager
Location: Onsite - San Diego, CA

Position Summary:

The Associate Regulatory Affairs Manager will support the development, review, and submission of regulatory documents for medical device and IVD products. This role will assist in managing regulatory projects, ensuring compliance with FDA, ISO 13485, and other global regulatory requirements. The Associate Manager will work cross-functionally with internal teams and external partners to support product approvals and maintain regulatory compliance throughout the product lifecycle.

Key Responsibilities:

Assist in the preparation, review, and submission of regulatory documentation for new products, product changes, and ongoing compliance.
Support the regulatory submission process for 510(k), Technical Files, and other regulatory filings.
Provide regulatory guidance to cross-functional teams during product development and post-market activities under the direction of senior management.
Help track and manage submission timelines, regulatory project plans, and documentation.
Stay informed on changes in FDA, ISO 13485, IVDR, and other global regulations, communicating relevant updates to the team.
Conduct regulatory assessments for product modifications and assist in defining appropriate submission strategies.
Participate in internal and external audits, inspections, and regulatory agency communications as assigned.
Contribute to the maintenance of regulatory files and submission records in accordance with internal procedures and regulations.
May provide oversight and mentorship to junior staff or specialists on assigned projects.

Requirements

Master’s degree in Regulatory Affairs, Life Sciences, Engineering, or a related field.
4–6 years supporting or managing 510(k) submissions and regulatory filings.
Experience participating in regulatory audits and inspections preferred.
Strong organizational, document management, and project coordination skills.
Excellent communication, problem-solving, and cross-functional collaboration abilities.
Detail-oriented with the ability to manage multiple regulatory projects and priorities.
Proficient in Microsoft Office and regulatory document management systems.
Ability to work independently and proactively while seeking guidance for complex issues.

Benefits

Highly competitive compensation package.
Comprehensive medical, dental, and vision insurance.
401(k) plan with generous company contributions.
Flexible paid time off (PTO) policy.
Additional substantial benefits.

Equal Opportunity Statement: We are an equal opportunity employer committed to inclusion and diversity. We do not discriminate based on race, gender, religion, sexual orientation, age, color, marital status, veteran status, disability status, national origin, or any other protected characteristic.

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associate manager jobs in poway ca

Associate Regulatory Affairs Manager (San Diego) - Bilingual (Mandarin Speaking)

Executive Recruiting - Sourcing Associate Manager

Associate Field Services Technology Manager

Associate Store Manager

Manager/ QA Associate, GxP Quality Systems

Oracle ICM Configuration Lead - Associate Manager

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