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Part Time Manager Cmc Regulatory Jobs (NOW HIRING)

Propedix, Inc.

Technical Project Manager

Irvine, CA · On-site +1

$5K - $6K/mo

Program Director/Technical Project Manager (part time) Position Overview: The Program Director ... Lead integrated program planning across R&D, CMC, regulatory, quality, supply chain, and marketing.

Propedix, Inc.

Technical Project Manager

Irvine, CA · On-site

$5K - $6K/mo

Program Director/Technical Project Manager (part time) Position Overview: The Program Director ... Lead integrated program planning across R&D, CMC, regulatory, quality, supply chain, and marketing.

Propedix, Inc.

Technical Project Manager

Irvine, CA · On-site

$5K - $6K/mo

Program Director/Technical Project Manager (part time) Position Overview: The Program Director ... Lead integrated program planning across R&D, CMC, regulatory, quality, supply chain, and marketing.

Thekey

Care Manager

Needham, MA

As a Part-Time Geriatric Care Manager, you are responsible to provide a holistic, client-centered ... Manager (CMC) or Certified Case Manager (CCM) Demonstrated knowledge of aging, dementia, and/or ...

TheKey

Care Manager

Needham, MA · On-site

As a Part-Time Geriatric Care Manager, you are responsible to provide a holistic, client-centered ... CMC) or Certified Case Manager (CCM) • Demonstrated knowledge of aging, dementia, and/or ...

North Memorial Health

Manager, Regulatory

Robbinsdale, MN · On-site

$50.64 - $63.29/hr

Manager, Regulatory Robbinsdale, MN Posting Date: May 29 2026 Requisition Number: 513720 Why North ... Most part-time and all full-time positions are eligible for benefits. * Health & Welfare Benefit ...

Comprehensive Mobile Care

Part-Time Dentist

Tucson, AZ

$900/wk

ASAP Compensation: $900 per visit Position Summary Comprehensive Mobile Care (CMC) is seeking a ... Diagnose and manage oral health conditions commonly seen in geriatric patients. * Educate patients ...

Claire's

Supervisor/Manager Part-Time

Danbury, CT · On-site

$21 - $23/hr

Claire's - A Career that's always in style Part-Time Manager/3rd Key Holder Opportunity About the ... regulations. All positions will be compensated at or above the legally mandated minimum wage for ...

Claire's

Supervisor/Manager Part-Time

Danbury, CT

$21 - $23/hr

Claire's - A Career that's always in style Part-Time Manager/3rd Key Holder Opportunity About the ... regulations. All positions will be compensated at or above the legally mandated minimum wage for ...

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Part Time Manager Cmc Regulatory information

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$54.5K

$110.7K

$182K

How much do part time manager cmc regulatory jobs pay per year?

As of Jun 12, 2026, the average yearly pay for part time manager cmc regulatory in the United States is $110,733.00, according to ZipRecruiter salary data. Most workers in this role earn between $77,500.00 and $136,500.00 per year, depending on experience, location, and employer.

What are the key skills and qualifications needed to thrive as a Part Time Manager CMC Regulatory, and why are they important?

To thrive as a Part Time Manager CMC Regulatory, you need a solid background in chemistry, manufacturing, and controls (CMC) regulations, along with experience in regulatory submissions for pharmaceuticals or biologics. Familiarity with regulatory databases, eCTD publishing tools, and knowledge of ICH guidelines are typically required, often supported by a relevant scientific degree. Strong project management, attention to detail, and effective communication help in coordinating cross-functional teams and ensuring regulatory compliance. These skills are crucial for ensuring timely product approvals and maintaining compliance with global regulatory standards.

What are some typical challenges faced by a Part Time Manager in CMC Regulatory, and how can they be effectively managed?

A Part Time Manager in CMC (Chemistry, Manufacturing, and Controls) Regulatory often faces challenges in balancing a flexible schedule with the fast-paced demands of regulatory submissions and project deadlines. Managing cross-functional communication is key, as the role requires close collaboration with manufacturing, quality, and R&D teams to gather and verify technical documentation. To be effective, it's important to set clear priorities, maintain organized records, and establish regular check-ins with stakeholders. Leveraging digital collaboration tools and being proactive in addressing potential compliance gaps can help ensure regulatory milestones are met without delays.

What does a Part Time Manager CMC Regulatory do?

A Part Time Manager CMC (Chemistry, Manufacturing, and Controls) Regulatory is responsible for ensuring that pharmaceutical products comply with regulatory requirements related to their manufacturing, quality, and documentation. This role involves preparing and reviewing CMC sections of regulatory submissions, coordinating with different departments to gather necessary data, and staying updated on changing regulations. As a part-time manager, they may handle these tasks on a reduced schedule, often supporting multiple projects or submissions. Their work is critical to obtaining and maintaining regulatory approval for drug products, ensuring patient safety and product quality.
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What cities are hiring for Part Time Manager Cmc Regulatory jobs? Cities with the most Part Time Manager Cmc Regulatory job openings:
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What job categories do people searching Part Time Manager Cmc Regulatory jobs look for? The top searched job categories for Part Time Manager Cmc Regulatory jobs are:
Part Time Manager Cmc Regulatory jobs near you
Infographic showing various Part Time Manager Cmc Regulatory job openings in the United States as of June 2026, with employment types broken down into 100% Part Time. Highlights an 100% In-person job distribution, with an average salary of $110,733 per year, or $53.2 per hour.
Intern - Regulatory Affairs, CMC (year-round)

Intern - Regulatory Affairs, CMC (year-round)

BeiGene, Inc.

Remote

Part-time

Medical, Dental, Vision, Life, Retirement, PTO

Posted 8 days ago

Job description

BeOne continues to grow at a rapid pace with challenging and exciting opportunities for experienced professionals. When considering candidates, we look for scientific and business professionals who are highly motivated, collaborative, and most importantly, share our passionate interest in fighting cancer.
General Description/Scope of Responsibilities (Internship):
BeOne is seeking a motivated and talented individual to join our Reg CMC small molecule team which offers meaningful project experiences that gives interns the opportunity to gain valuable Biotech experience as they complete their academic journey.
The Regulatory Affairs CMC Intern will support regulatory projects consistent with company goals by working closely with the hiring manager and cross-functional team members, including Quality Assurance, Supply Chain, CMC, and IT. The focus of the internship is for the intern to develop a deeper understanding of the drug development process and regulatory requirements in a professional work environment, while contributing to process optimization in knowledge management. Specifically, the intern will:
  • Be exposed to the broad scope of global Regulatory Affairs and specifically CMC Regulatory Affairs and the role's contribution to drug development and patients' access to medicines.
  • Learn about the role of global Health Authorities in the drug development process.
  • Gain hands-on experience in preparing regulatory documents for submission to global health authorities.
  • Acquire knowledge about the differences in regulatory requirements across regions.
  • Experience CMC technical product development and manufacturing functions in relation to regulatory affairs.

Essential Functions of the Internship:
  • Responsible for maintaining accurate CMC information in the BeOne Regulatory Information Management system
  • Data remediation
  • Create and maintain CMC Submission Content
  • Upload HA Correspondence/HA Questions/Commitments
  • Maintain internal Regulatory CMC trackers
  • Contribute to Reg CMC process improvements
  • Support the drafting of CTD CMC sections to ensure on-time and high-quality global applications for direct submission to Health Authorities as needed.
  • Provide support to Reg CMC team or hiring manager with Regulatory submissions and other tasks as needed

Supervisory Responsibilities:
  • No

Computer Skills: Proficient in Microsoft Office
Education Required: Active enrollment (Graduate or Ph.D.) in an accredited college or university pursing a degree in a scientific discipline (e.g., life sciences, chemistry, biology, biotechnology, materials science, etc.) with a minimum 3.0 GPA
Other Qualifications:
  • Awareness of processes for working in a regulated field preferred
  • Basic knowledge of healthcare industry and strong passion for biotech
  • Legally authorized to work in the United States without needing sponsorship for employment now or in the future
  • Ability to work independently on assignments with routine check-ins
  • Strong written and oral communication skills
  • Organized, responsible, resourceful, and detail-oriented
  • Able to work in a cross-cultural team environment with members across different time zones
  • Able to work remotely using MS TEAMS and other collaboration tools

Travel: None
Global Competencies
When we exhibit our values of Patients First, Driving Excellence, Bold Ingenuity and Collaborative Spirit, through our twelve global competencies below, we help get more affordable medicines to more patients around the world.
  • Fosters Teamwork
  • Provides and Solicits Honest and Actionable Feedback
  • Self-Awareness
  • Acts Inclusively
  • Demonstrates Initiative
  • Entrepreneurial Mindset
  • Continuous Learning
  • Embraces Change
  • Results-Oriented
  • Analytical Thinking/Data Analysis
  • Financial Excellence
  • Communicates with Clarity

Salary Range: $ - $ per hour
BeOne is committed to fair and equitable compensation practices. Actual compensation packages are determined by several factors that are unique to each candidate, including but not limited to job-related skills, depth of experience, certifications, relevant education or training, and specific work location. Packages may vary by location due to differences in the cost of labor. The recruiter can share more about the specific salary range for a preferred location during the hiring process. Please note that the listed range reflects the base salary or hourly range only. Non-Commercial roles are eligible to participate in the annual bonus plan, and Commercial roles are eligible to participate in an incentive compensation plan. All Company employees have the opportunity to own shares of BeOne Medicines Ltd. stock because all employees are eligible for discretionary equity awards and to voluntarily participate in the Employee Stock Purchase Plan. The Company has a comprehensive benefits package that includes Medical, Dental, Vision, 401(k), FSA/HSA, Life Insurance, Paid Time Off, and Wellness.
We are proud to be an equal opportunity employer. BeOne does not discriminate on the basis of race, religion, color, sex, gender identity, sexual orientation, age, disability, national origin, veteran status or any other basis covered by appropriate law. All employment is decided on the basis of qualifications, merit, and business need. In order to ensure reasonable accommodation for individuals protected by Section 503 of the Rehabilitation Act of 1973, the Vietnam Era Veterans' Readjustment Assistance Act of 1974, Title I of the Americans with Disabilities Act of 1990, and any other applicable federal, state or local laws, applicants who require reasonable accommodation in the job application process may contact accommodationsus@beonemed.com.
BeiGene logo

About BeiGene

Sourced by ZipRecruiter

BeiGene (NASDAQ: BGNE; HKEX: 06160; SSE: 688235) is a global, science-driven biotechnology company focused on developing innovative and affordable medicines to improve treatment outcomes and access for patients worldwide. With a broad portfolio of more than 40 clinical candidates, we are expediting development of our diverse pipeline of novel therapeutics through our own capabilities and collaborations. We are committed to radically improving access to medicines for two billion more people by 2030. BeiGene has a growing global team of over 8,200 colleagues across five continents. For more information, please visit www.beigene.com .

Industry

Health care and social assistance

Company size

5,001 - 10,000 Employees

Headquarters location

Cambridge, MA, US

Year founded

2010

Social media

Twitter

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