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Weekday Capacity Development Jobs (NOW HIRING)

First & 42

Development & Campaign Manager

Portage, MI · On-site

... capacity needed to support the institution's long-term philanthropic growth. Working closely with ... Schedule/Work Hours Full-time position with primarily weekday business hours. Occasional evenings ...

PPG

Superintendent, Weekday Night

Cleveland, OH · On-site

$100K - $115K/yr

Develop productivity/capacity plans for materials, machines, and employees and develop plans for ... Lead team of Production Supervisors and ensure development through coaching. * Manage product ...

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Weekday Capacity Development information

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$92K

How much do weekday capacity development jobs pay per year?

As of Sep 14, 2026, the average yearly pay for weekday capacity development in the United States is $55,773.00, according to ZipRecruiter salary data. Most workers in this role earn between $44,500.00 and $61,000.00 per year, depending on experience, location, and employer.

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Weekday Capacity Development jobs near you

Research and Development Project Manager

San Clemente, CA • Hybrid

Weekday AI
Human Resources Consulting Services • 11 - 50 employees
Learn more about Weekday AIexternal

Full-time

Re-posted 15 days ago

Job description

This role is for one of the Weekday's clients

Now Hiring: Senior Project Manager - R&D | Medical Device New Product Development
San Clemente, CA (Hybrid)
Competitive Salary | Long-Term Role

Various shifts might be available, with compensation varying based on the selected shift.

We are currently looking for a seasoned Senior Project Manager with extensive experience in Medical Device New Product Development (NPD) to lead enterprise-level R&D projects within a highly regulated healthcare setting.

The successful candidate should possess practical expertise in managing products throughout the entire medical device development process - including design inputs, verification and validation, regulatory submissions, and product launch.

Requirements

Qualifications We Seek:
Extensive experience in Medical Device New Product Development (NPD)
In-depth knowledge of Design Controls
Proven background in supporting FDA 510(k), MDR, and other regulatory submissions
Capacity to perform effectively in fast-paced and ambiguous R&D settings
Demonstrated track record of driving alignment across cross-functional teams including R&D, Regulatory, Quality, Operations, and Supply Chain
Experience with supporting product launch and ongoing sustaining engineering efforts

Primary Responsibilities:
Lead complex R&D and New Product Development initiatives within FDA-regulated contexts
Oversee project execution from initial concept through to commercialization
Manage schedules, budgets, resources, risks, and deliverables associated with projects
Coordinate multidisciplinary teams such as Regulatory Affairs, Quality, Manufacturing, Operations, Marketing, and Supply Chain
Support design control activities, including product performance, assembly integrity, safety, labeling, packaging, as well as verification and validation tasks
Collaborate with stakeholders to establish project scope, validation strategies, and requirements in dynamic development environments
Ensure compliance of all projects with FDA, ISO 13485, GMP, and MDR standards
Deliver executive-level project status updates and communications

Required Qualifications:
Bachelor's degree mandatory
Minimum of 4 years' experience in Project Management within Medical Device or regulated healthcare industries
Experience in Design Controls and Medical Device Development Lifecycle
Strong comprehension of NPD processes and regulatory frameworks
Skilled in MS Project, Excel, PowerPoint, SharePoint, and other related project management tools

This role represents a fantastic opportunity for a self-driven individual who excels in early-stage product development and can lead execution across multiple teams independently.

Must-have skills

R&D medical device Medical Devices Medical Device R&D Biomedical Device Design Biomedical Devices

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