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US Browse · Alameda · Other - Healthcare

Other - Healthcare in Alameda

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Director, Medical Events Group & Npr – Abbott Diabetes Care
Abbott
Alameda, California, United States
Full time
Base: $172,000.00 – $344,000.00; bonus/equity: not...
Not specified
Global medical device reporting regulations
Fda iso 13485 eu mdr compliance
Post-market surveillance leadership
The Director will lead global medical device vigilance and post-market surveillance ensuring worldwide compliance with FDA, ISO 13485, and EU MDR standards
39 days ago
Complaint Investigation Technician (first Shift)
Abbott
Alameda, California, United States
Full time
Base: $25.00 – $50.00ph; bonus/equity: not specifi...
Fully onsite
+2y experience
Routine laboratory testing of medical devices
Documenting investigation activities accurately
Handling multiple tasks efficiently
The Complaint Investigation Technician will perform routine testing in a laboratory setting of medical devices associated with returns due to customer complaints while ensuring timely closure
39 days ago
Senior Manager Clinical Operations
Abbott
Alameda, California, United States
Full time
Base: $148,700.00 – $297,300.00; bonus/equity: not...
Hybrid
Senior
10+ years in clinical research
5+ years in clinical operations leadership
Site/lab/cro startup and activation experience
This strategic leadership role ensures timely activation, operational excellence, and quality compliance for clinical programs across the Diabetes Care division
39 days ago
Principal Regulatory Affairs Specialist (business Partnerships).
Abbott
Alameda, California, United States
Full time
Base: $100,000.00 – $200,000.00; bonus/equity: not...
Onsite
Senior
Bachelor's degree in scientific discipline
Experience with regulatory submissions for medical devices
Knowledge of 21 cfr 820 and iso 13485 standards
This role involves developing global regulatory strategies for strategic business initiatives involving cloud and sensor-based external partnerships within the Diabetes Care Division
39 days ago
Senior Specialist Regulatory Affairs
Abbott
Alameda, California, United States
Full time
Base: $86,700.00 – $173,300.00; bonus/equity: not ...
**
Senior
Review labeling advertising and promotional materials
Ensure compliance with regulatory agency guidelines
Support product development for digital health products
This role supports the commercialization of new digital products including generative AI technologies designed to help millions of patients
39 days ago
Ehr Implementation Manager
Abbott
Alameda, California, United States
Full time
Base: $128,000.00 – $256,000.00; bonus/equity: not...
Onsite
+6y experience
3+ years healthcare experience
Bachelor's degree or mba
Strategic partnership execution
This role is part of the FreeStyle Libre Ecosystem and Strategic Partnerships team within Abbott Diabetes Care
39 days ago
Senior Director, Customer Innovation And Product Management
Abbott
Alameda, California, United States
Full time
Base: $218,700.00 – $437,300.00; bonus/equity: not...
**
10 years relevant business experience
Bachelor's degree in engineering or basic science
Sound understanding of regulated markets
This role leads the Innovation and Product Management team within Abbott Diabetes Care to identify and advance new products from conception through engineering specification
42 days ago
Specialist Regulatory Affairs
Abbott
Alameda, California, United States
Full time
Base: $81,500.00 – $141,300.00; bonus/equity: not ...
Onsite
+2y experience
Review labeling and promotional materials
Coordinate regulatory advertising activities
Support digital product development submissions
This role supports the commercialization of new digital products and features including generative AI technologies designed to help millions of patients
42 days ago
Supervisor Complaint Handling
Abbott
Alameda, CA, United States
Full time
Base: $100,000.00 – $200,000.00; bonus/equity: not...
**
+4y experience
Minimum 4 years quality experience
Experience in regulated environment
Leading non-exempt employees
The role involves direct supervision of non-exempt employees evaluating and closing customer complaint cases for Abbott Diabetes Care products
44 days ago
Clinical Data Manager
Abbott
Alameda, CA, United States
Full time
Base: $90,000.00 – $180,000.00; bonus/equity: not ...
**
+4y experience
4+ years clinical or medical research experience
Expert sql query skills for data sets
Electronic data capture system proficiency
This role is critical to the successful collection, reporting, and analysis of clinical trial data within the Abbott Diabetes Care Division
44 days ago
Principal International Regulatory Product Specialist - Diabetes Care (on-site)
Abbott
Alameda, California, United States
Full time
Base: $100,000.00 – $200,000.00; bonus/equity: not...
On-site
Senior
Bachelor's degree in scientific discipline
Experience in regulatory submissions
Knowledge of 21 cfr 820 and iso 13485
This role involves working on-site at the Alameda, CA location to ensure efficient and compliant business processes within the Diabetes Care Division
46 days ago
Specialist Regulatory Affairs
Abbott
Alameda, CA, United States
Full time
Base: $81,500.00 – $141,300.00; bonus/equity: not ...
Onsite
+2y experience
Review labeling and promotional materials
Coordinate regulatory advertising activities
Support digital product development teams
This role supports the commercialization of new digital products and features including generative AI technologies designed to help millions of patients in the US
49 days ago
Regulatory Affairs Manager - International Compliance Operations – Diabetes Care (on-site)
Abbott
Alameda, CA, United States
Full time
Base: $114,000.00 – $228,000.00; bonus/equity: not...
On-site
+8y experience
8 years medical device industry experience
5 years fda submission preparation
Class i ii iii device regulatory knowledge
This role provides end-to-end support for the regulatory department to ensure efficient and compliant business processes within the Diabetes Care Division
49 days ago
Gsm Director, Business Data Strategy
Abbott
Alameda, California, United States
Full time
Base: $197,300.00 – $394,700.00; bonus/equity: not...
**
Data governance and ethics leadership
Regulated medical device environment experience
End-to-end data product ownership
The role leads the development of a comprehensive data strategy roadmap within Abbott Diabetes Care to improve product quality and customer experience
49 days ago
Principal Regulatory Affairs Specialist – Apac - Diabetes Care (on-site)
Abbott
Alameda, CA, United States
Full time
Base: $100,000.00 – $200,000.00; bonus/equity: not...
On-site
Senior
Bachelor's degree in scientific discipline
Experience with 21 cfr 820 and iso 13485
Strategic planning for product registration
This role leads strategic planning to ensure timely regulatory registration and release of diabetes care products into the Asia Pacific market
49 days ago
Regulatory Affairs Manager – Apac - Diabetes Care (on-site)
Abbott
Alameda, CA, United States
Full time
Base: $114,000.00 – $228,000.00; bonus/equity: not...
On-site
+5y experience
Manage regulatory specialists team
Develop global regulatory strategies
Prepare medical device submissions
This role involves managing a small team to oversee the Diabetes Care product portfolio in the Asia Pacific region while ensuring efficient and compliant business processes
49 days ago
Laboratory Operations Associate I - Facilities
iQ Biosciences
Alameda, CA, US
**
Equipment maintenance and calibration
Temperature monitoring of freezers
Liquid nitrogen handling
The role supports laboratory operations with a primary focus on maintaining lab equipment and facilities to enable preclinical research studies
51 days ago
Senior Manager Medical Affairs
Abbott
Alameda, CA, United States
Full time
Base: $130,700.00 – $261,300.00; bonus/equity: not...
Hybrid (25% travel)
Senior
Expertise in cardiometabolic health
Experience with continuous monitoring devices
Manage global cross-functional teams
The Senior Manager will lead medical affairs activities for Lingo, a new biosensing technology tracking biomarkers like glucose and ketones
52 days ago
Principal Regulatory Affairs Specialist – Diabetes Care (on-site)
Abbott
Alameda, CA, United States
Full time
Base: $100,000.00 – $200,000.00; bonus/equity: not...
On-site
Senior
Us submissions for in vitro diagnostic devices
Experience with 21 cfr 820 and iso 13485
Medical device regulation (2017/745) knowledge
The Principal Regulatory Affairs Specialist will develop global regulatory strategies for continuous glucose monitoring systems and new product introductions
52 days ago
Senior Manager Medical Affairs
Abbott
Alameda, CA, United States
Full time
Base: $130,700.00 – $261,300.00; bonus/equity: not...
Senior
Expertise in cardiometabolic health
Experience with continuous monitoring devices
Global cross-functional team collaboration
This role supports the Lingo division's mission to democratize healthcare through biosensing technology that tracks biomarkers like glucose and ketones
52 days ago
Principal Regulatory Affairs Specialist – Diabetes Care (on-site)
Abbott
Alameda, CA, United States
Full time
Base: $100,000.00 – $200,000.00; bonus/equity: not...
**
Senior
Us regulatory submissions experience
In vitro diagnostic devices knowledge
21 cfr 820 compliance expertise
Abbott is a global healthcare leader focused on revolutionizing glucose monitoring with new sensing technology for people with diabetes
52 days ago
Specialist Regulatory Affairs
Abbott
Alameda, CA, US
Full time
Base: $81,500.00 – $141,300.00; bonus/equity: not ...
+13y experience
Review labeling advertising promotional materials
Support regulatory submissions for digital products
Collaborate with software development teams
This role supports the commercialization of new digital products and features including generative AI technologies designed to help millions of patients
52 days ago
Manager, Product Quality Engineering
AbbVie
Alameda, CA, United States
Full time
$114,000.00 – $228,000.00 py
**
+6y experience
Product complaint investigations
Capa system ownership
Post-market surveillance
Responsible for initiating and owning investigations associated with trends and emerging issues with product complaints, captured in the CAPA system
53 days ago
Clinical Research, Associate I
AbbVie
Alameda, California, United States
Full time
Base: $73,900.00 – $116,000.00; bonus/equity: not ...
**
+2y experience
Ich gcp
Iso 14155
Study site visits
The CRA will ensure quality, accuracy and integrity of clinical trial data throughout the full lifecycle of multiple clinical trials according to the Code of Federal Regulations, ICH GCP, and ISO14155
64 days ago
Senior Manager Medical Affairs
AbbVie
Alameda, California, United States
Full time
Base: $130,700.00 – $261,300.00; bonus/equity: not...
Senior
Expertise in cardiometabolic health
Experience with continuous monitoring devices
Cross-functional team collaboration
Abbott is a global healthcare leader that helps people live more fully at all stages of life with a diverse portfolio including diagnostics, medical devices, and nutritionals
75 days ago

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Other - Healthcare in Alameda

Director, Medical Events Group & Npr – Abbott Diabetes Care

Complaint Investigation Technician (first Shift)

Senior Manager Clinical Operations

Principal Regulatory Affairs Specialist (business Partnerships).

Senior Specialist Regulatory Affairs

Ehr Implementation Manager

Senior Director, Customer Innovation And Product Management

Specialist Regulatory Affairs

Supervisor Complaint Handling

Clinical Data Manager

Principal International Regulatory Product Specialist - Diabetes Care (on-site)

Specialist Regulatory Affairs

Regulatory Affairs Manager - International Compliance Operations – Diabetes Care (on-site)

Gsm Director, Business Data Strategy

Principal Regulatory Affairs Specialist – Apac - Diabetes Care (on-site)

Regulatory Affairs Manager – Apac - Diabetes Care (on-site)

Laboratory Operations Associate I - Facilities

Senior Manager Medical Affairs

Principal Regulatory Affairs Specialist – Diabetes Care (on-site)

Senior Manager Medical Affairs

Principal Regulatory Affairs Specialist – Diabetes Care (on-site)

Specialist Regulatory Affairs

Manager, Product Quality Engineering

Clinical Research, Associate I

Senior Manager Medical Affairs