Represent CSL in official regulatory CMC capacities, acting as an authorized official or ... Maintain strong, positive relationships with regulators and ensure timely responses to inquiries ...
Represent CSL in official regulatory CMC capacities, acting as an authorized official or ... Maintain strong, positive relationships with regulators and ensure timely responses to inquiries ...
GRA CMC Specialist
King Of Prussia, PA · On-site
Represent CSL in official regulatory CMC capacities, acting as an authorized official or ... Maintain strong, positive relationships with regulators and ensure timely responses to inquiries ...
GRA CMC Specialist
King Of Prussia, PA · On-site
Represent CSL in official regulatory CMC capacities, acting as an authorized official or ... Maintain strong, positive relationships with regulators and ensure timely responses to inquiries ...
GRA CMC Specialist
King Of Prussia, PA · On-site
Represent CSL in official regulatory CMC capacities, acting as an authorized official or ... Maintain strong, positive relationships with regulators and ensure timely responses to inquiries ...
GRA CMC Specialist
King Of Prussia, PA · On-site
Represent CSL in official regulatory CMC capacities, acting as an authorized official or ... Maintain strong, positive relationships with regulators and ensure timely responses to inquiries ...
Senior Director, Regulatory CMC
South San Francisco, CA · On-site
$260 - $295/hr
Maintain CMC Regulatory document control system * Monitor regulatory guidelines and trends related to CMC; interpret regulations and guidance to provide advice to company leadership and CMC teams
Senior Director, Regulatory CMC
South San Francisco, CA · On-site
$260 - $295/hr
Maintain CMC Regulatory document control system * Monitor regulatory guidelines and trends related to CMC; interpret regulations and guidance to provide advice to company leadership and CMC teams
Software Developer Strategy CMC
$75 - $85/hr
Maintain the Strategy CMC application and supporting containerized infrastructure post-deployment * Develop operational procedures, documentation, and best practices for long-term support * Mentor ...
Software Developer Strategy CMC
$75 - $85/hr
Maintain the Strategy CMC application and supporting containerized infrastructure post-deployment * Develop operational procedures, documentation, and best practices for long-term support * Mentor ...
Director, RA CMC
Irvine, CA · On-site
$140 - $180/hr
Medical
Dental
Vision
Retirement
PTO
Builds and maintains relationships within the Regulatory Affairs functional areas and the Operations and Research & Development (R&D) organizations. Represents RA CMC on product development and life ...
Director, RA CMC
Irvine, CA · On-site
$140 - $180/hr
Medical
Dental
Vision
Retirement
PTO
Builds and maintains relationships within the Regulatory Affairs functional areas and the Operations and Research & Development (R&D) organizations. Represents RA CMC on product development and life ...
GRA CMC Specialist
King Of Prussia, PA · On-site
Represent CSL in official regulatory CMC capacities, acting as an authorized official or ... Maintain strong, positive relationships with regulators and ensure timely responses to inquiries ...
GRA CMC Specialist
King Of Prussia, PA · On-site
Represent CSL in official regulatory CMC capacities, acting as an authorized official or ... Maintain strong, positive relationships with regulators and ensure timely responses to inquiries ...
Director, Regulatory CMC
South San Francisco, CA · On-site
$275K - $280K/yr
Design and implement innovative global CMC regulatory strategies to secure approvals and maintain compliance for clinical and commercial products, identifying potential risks and creating robust ...
Director, Regulatory CMC
South San Francisco, CA · On-site
$275K - $280K/yr
Design and implement innovative global CMC regulatory strategies to secure approvals and maintain compliance for clinical and commercial products, identifying potential risks and creating robust ...
Senior Director, Regulatory CMC
South San Francisco, CA · On-site
$260K - $295K/yr
Maintain CMC Regulatory document control system * Monitor regulatory guidelines and trends related to CMC; interpret regulations and guidance to provide advice to company leadership and CMC teams
Senior Director, Regulatory CMC
South San Francisco, CA · On-site
$260K - $295K/yr
Maintain CMC Regulatory document control system * Monitor regulatory guidelines and trends related to CMC; interpret regulations and guidance to provide advice to company leadership and CMC teams
Associate II, CMC Operations
Waltham, MA · On-site
Support the Associate Director, CMC Operations by maintaining and updating appropriate CMC tracking tools, proactively communicating key issues and other critical topics, and escalating concerns in a ...
Associate II, CMC Operations
Waltham, MA · On-site
Support the Associate Director, CMC Operations by maintaining and updating appropriate CMC tracking tools, proactively communicating key issues and other critical topics, and escalating concerns in a ...
Sr. Director, Regulatory CMC
Somerville, MA · Hybrid
$163K - $216K/yr
... while maintaining product supply and inspection readiness. The Senior Director serves as a key ... Own and drive global CMC change management strategy, assessing manufacturing, analytical, raw ...
Sr. Director, Regulatory CMC
Somerville, MA · Hybrid
$163K - $216K/yr
... while maintaining product supply and inspection readiness. The Senior Director serves as a key ... Own and drive global CMC change management strategy, assessing manufacturing, analytical, raw ...
Senior Director, Regulatory CMC
South San Francisco, CA · On-site
$245K - $285K/yr
Maintain a centralized archive for tracking and monitoring the status of regulatory CMC commitments and agency reporting obligations. Create and issue status reports and other communication to the ...
Senior Director, Regulatory CMC
South San Francisco, CA · On-site
$245K - $285K/yr
Maintain a centralized archive for tracking and monitoring the status of regulatory CMC commitments and agency reporting obligations. Create and issue status reports and other communication to the ...
Senior Director, Regulatory CMC
South San Francisco, CA · On-site
$245K - $285K/yr
Maintain a centralized archive for tracking and monitoring the status of regulatory CMC commitments and agency reporting obligations. Create and issue status reports and other communication to the ...
Quick apply
Senior Director, Regulatory CMC
South San Francisco, CA · On-site
$245K - $285K/yr
Maintain a centralized archive for tracking and monitoring the status of regulatory CMC commitments and agency reporting obligations. Create and issue status reports and other communication to the ...
Director Regulatory Affairs (CMC)
$158K - $209K/yr
Lead all RA-CMC operations through all phases of clinical development; from FIH through post-approval maintenance. * Communicate and collaborate with global counterparts effectively, ensuring ...
Quick apply
Director Regulatory Affairs (CMC)
$158K - $209K/yr
Lead all RA-CMC operations through all phases of clinical development; from FIH through post-approval maintenance. * Communicate and collaborate with global counterparts effectively, ensuring ...
Director, CMC Stability
Norwood, MA · On-site
$167 - $300.70/hr
PTO
Build and maintain effective stability operating models, governance, and decision forums that ... CMC control strategies. * Oversee authoring and review of stability sections for regulatory ...
Director, CMC Stability
Norwood, MA · On-site
$167 - $300.70/hr
PTO
Build and maintain effective stability operating models, governance, and decision forums that ... CMC control strategies. * Oversee authoring and review of stability sections for regulatory ...
Senior Director, Regulatory CMC
South San Francisco, CA · On-site
$180K - $237K/yr
Maintain CMC Regulatory document control system * Monitor regulatory guidelines and trends related to CMC; interpret regulations and guidance to provide advice to company leadership and CMC teams
Senior Director, Regulatory CMC
South San Francisco, CA · On-site
$180K - $237K/yr
Maintain CMC Regulatory document control system * Monitor regulatory guidelines and trends related to CMC; interpret regulations and guidance to provide advice to company leadership and CMC teams
Director, Regulatory CMC
South San Francisco, CA · On-site
$275K - $280K/yr
Design and implement innovative global CMC regulatory strategies to secure approvals and maintain compliance for clinical and commercial products, identifying potential risks and creating robust ...
Director, Regulatory CMC
South San Francisco, CA · On-site
$275K - $280K/yr
Design and implement innovative global CMC regulatory strategies to secure approvals and maintain compliance for clinical and commercial products, identifying potential risks and creating robust ...
Lead the preparation and maintenance of the CMC / quality sections for regulatory submissions including initial submission of IND, IMPD/CTA, NDA, MAA and amendments to Health Authorities (HAs), and ...
Lead the preparation and maintenance of the CMC / quality sections for regulatory submissions including initial submission of IND, IMPD/CTA, NDA, MAA and amendments to Health Authorities (HAs), and ...
Director, RA CMC
North Chicago, IL · On-site
$144K - $190K/yr
Medical
Dental
Vision
Retirement
PTO
Builds and maintains relationships within the Regulatory Affairs functional areas and the Operations and Research & Development (R&D) organizations. Represents RA CMC on product development and life ...
Director, RA CMC
North Chicago, IL · On-site
$144K - $190K/yr
Medical
Dental
Vision
Retirement
PTO
Builds and maintains relationships within the Regulatory Affairs functional areas and the Operations and Research & Development (R&D) organizations. Represents RA CMC on product development and life ...
Director, Global CMC Regulatory
$153K - $202K/yr
The Director, Global CMC Regulatory is a strategic leadership role responsible for developing, driving, and executing global commercial CMC regulatory strategies to secure and maintain marketing ...
Director, Global CMC Regulatory
$153K - $202K/yr
The Director, Global CMC Regulatory is a strategic leadership role responsible for developing, driving, and executing global commercial CMC regulatory strategies to secure and maintain marketing ...
Cmc Maintenance information
See salary details
$12.50 - $16.48
4% of jobs
$16.48 - $20.45
12% of jobs
$22.77 is the 25th percentile. Wages below this are outliers.
$20.45 - $24.43
16% of jobs
The median wage is $28.30 / hr.
$24.43 - $28.41
19% of jobs
$28.41 - $32.39
15% of jobs
$36.07 is the 75th percentile. Wages above this are outliers.
$32.39 - $36.36
11% of jobs
$36.36 - $40.34
7% of jobs
$40.34 - $44.32
7% of jobs
$44.32 - $48.30
4% of jobs
$48.30 - $52.27
3% of jobs
$52.27 - $56.25
2% of jobs
$12
$31
$56
How much do cmc maintenance jobs pay per hour?
What is the difference between Cmc Maintenance vs Cmc Technician?
| Aspect | Cmc Maintenance | Cmc Technician |
|---|---|---|
| Certifications | Typically requires certifications in maintenance, HVAC, or electrical systems | Often requires similar certifications, focusing on hands-on technical skills |
| Work Environment | Maintenance teams, industrial or commercial facilities | Fieldwork, repair shops, or on-site at facilities |
| Employer & Industry Usage | Used by facilities management, manufacturing, and industrial companies | Commonly used in similar industries, focusing on technical repair roles |
Both Cmc Maintenance and Cmc Technician roles involve technical skills, certifications, and work in industrial or commercial settings. The main difference lies in the scope: Cmc Maintenance often refers to broader maintenance responsibilities, while Cmc Technician typically emphasizes hands-on repair and troubleshooting tasks.
What is a CMC Maintenance job?
What are the key skills and qualifications needed to thrive as a CMC Maintenance technician?
What are some of the common challenges faced by CMC Maintenance professionals and how can they be addressed?
What cities are hiring for Cmc Maintenance jobs?
Cities with the most Cmc Maintenance job openings:
What are the most commonly searched types of Cmc Maintenance jobs?
The most popular types of Cmc Maintenance jobs are:
What states have the most Cmc Maintenance jobs?
States with the most job openings for Cmc Maintenance jobs include:
What job categories do people searching Cmc Maintenance jobs look for?
The top searched job categories for Cmc Maintenance jobs are:

Job description
Team Lead, Global Regulatory Affairs x 2
The Team Lead, Global Regulatory Affairs CMC - Biological & Non-Biol. Products is responsible for:
Partnering closely with CSL’s R&D, Manufacturing, Quality, Regulatory Affairs stakeholders to address regulatory strategy challenges and deliver innovative, timely regulatory solutions that meet evolving CMC regulatory and compliance requirements for the assigned product portfolio.
Defining global regulatory strategies, objectives, and policies that advance and support the development, registration, and lifecycle management of CSL’s biological & non-biol. products.
Represent CSL in official regulatory CMC capacities, acting as an authorized official or responsible person in interactions with regulatory agencies.
This role promotes strong cross-functional collaboration and effective communication across Global Operations, R&D, Global Regulatory Affairs, and other relevant CSL business functions to drive alignment and support CSL’s strategic business objectives.
Reporting relationships
- Role that this position reports to: Team Lead, Global Regulatory Affairs CMC - Biological & Non-Biol. Products
- Role/s that report to this position: N/a
Main Responsibilities and Accountabilities
- Lead the global regulatory CMC strategy across the assigned development and commercial biological & non-biol. product portfolio, collaborating closely with cross-functional leaders in Global Regulatory Affairs CMC, Global Regulatory Affairs, R&D, Quality, Global Operations, and other business functions.
- Manage the development and submission of high-quality, compliant CMC regulatory submissions and submission components, including new marketing applications, clinical trial applications, variations/supplements, periodic compliance reports and renewals. Ensure timely execution aligned with regulatory expectations and business goals.
- Ensure accurate and timely change control assessments of change control notifications in CSL’s quality management system for biological & non-biol. product-related change controls. This includes the country-specific reporting category and detailed submission documentation requirements.
- Leverage external insights to refine strategies and implement innovative regulatory approaches that enhance CSL’s competitive positioning for its biological & non-biol. product portfolio.
- Represent CSL in official regulatory CMC capacities, acting as an authorized official or responsible person in interactions with regulatory agencies. Maintain strong, positive relationships with regulators and ensure timely responses to inquiries and requests. Facilitate timely decision-making and guidance from health authorities through effective communication and relationship management.
- Develop strategic and tactical plans for Global Regulatory Affairs CMC, advising Global Regulatory Affairs CMC leadership and CSL stakeholders on regulatory requirements and their implications for project timelines, compliance, and business strategy. Contribute to the evaluation of new business opportunities in collaboration with development teams.
- Provide regulatory consultation to internal CSL functions, including Global Operation functions, R&D, and IT, to support the design and implementation of business processes that ensure regulatory compliance and operational excellence.
- Provides tactical and strategic regulatory input and guidance, including active participation in problem solving analysis by assessing and proposing alternative solutions to issues and prepare contingency plans while still meeting regulations.
- Maintains an ongoing and interactive relationship with regional and local regulatory teams to assure that all aspects of the company’s regulatory activities are conducted in full compliance with applicable regulations and at the highest level of ethical standards.
- Ensure regulatory policies and procedures are developed and implemented in accordance with applicable international standards and requirements.
- Support the creation and execution of regulatory policies, processes, and SOPs that meet global regulatory requirements while driving operational efficiency and effectiveness across Global Operations and its stakeholder network.
- Support the outsourcing of regulatory activities, including submission quality assurance, to ensure timely and compliant delivery of services aligned with business and regulatory requirements.
Position Qualifications and Experience Requirements
Education & Experience
- A bachelor’s degree in biological or chemical sciences, or a related field is required; an advanced degree (e.g., MS, PhD) is strongly preferred.
- Over 5 years of progressive experience in regulatory roles within the biologics or plasma industry, demonstrating increasing levels of responsibility.
- Strong technical foundation with in-depth knowledge of global regulations and international standards governing drug product development, manufacture, registrations, and life-cycle management.
- Proven expertise in authoring, reviewing, and managing regulatory submissions ensuring accuracy, compliance, and timely delivery.
- Demonstrated ability to lead cross-functional teams and collaborate effectively with key stakeholders.
- For the Level 6 and Level 7 roles, skilled in motivating, mentoring, and guiding diverse teams within a matrixed organizational structure, fostering a culture of accountability and excellence.
- Skilled in motivating, mentoring, and guiding diverse teams within a matrixed organizational structure, fostering a culture of accountability and excellence.
- Exceptional oral and written communication skills, with a strong ability to negotiate, influence, and represent regulatory positions effectively.
- Committed to the highest standards of compliance, integrity, and adaptability, with a strong focus on aligning regulatory strategy with evolving business needs.
- Ability to use precedent and previous experience to develop innovative and flexible approaches to achieve goals.
Competencies
- Ensures Accountability: Follows through on commitments and makes sure others do the same; Acts with a clear sense of ownership; Takes personal responsibility for decisions, actions, and failures; Establishes clear responsibilities and processes for monitoring work and measuring results; Designs feedback loops into work.
- Drives Results: Has a strong bottom-line orientation; Persists in accomplishing objectives despite obstacles and setbacks; Has a track record of exceeding goals successfully; Pushes self and helps others achieve results.
- Drives Vision & Purpose: Talks about future possibilities in a positive way; Creates milestones and symbols to rally support behind the vision; Articulates the vision in a way everyone can relate to; Creates organization-wide energy and optimism for the future; Shows personal commitment to the vision.
- Instills Trust: Follows through on commitments; Is seen as direct and truthful; Keeps confidences; Practices what he/she preaches; Shows consistent between words and actions.
- Communicates Effectively: Is effective in a variety of communication settings: one-on-one, small and large groups, among diverse styles and position levels, with internal and external stakeholders/audiences. Attentively listens to others; Adjusts to fit the audience and the message; Provides timely and helpful information to others across the organization; Encourages the open expression of diverse ideas and opinions.
- Builds Effective Teams: Establishes common objectives and a shared mindset; Creates a feelings of belonging and strong team morale; Shares wins and rewards team efforts; Fosters open dialogue and collaboration among the team.
- Drives Engagement: Structures the work so it aligns with people's goals and motivators; Empowers others; Makes each person feel his/her contributions are important; Invites input and shares ownership and visibility; Shows a clear connection between people's motivators and the organizational goals.
- Manages Ambiguity: Deals comfortably with the uncertainty of change; Effectively handles risk; Can decide and act without the total picture; Is calm and productive, even when things are up in the air; Deals constructively with problems that do not have clear solutions or outcomes.
- Collaborates: Works cooperatively with others across the site, matrix, network and enterprise to achieve shared objectives; Represents own interests while being fair to others and their areas; Partners with others to get work done; Credits others for their contributions and accomplishments; Gains trust and support of others.
- Decision Quality: Makes sound decisions, even in the absence of complete information; Relies on a mixture of analysis, wisdom, experience, and judgment when making decisions; Considers all relevant factors and uses appropriate decision-making criteria and principles; Recognizes when a quick 80% solution will suffice.
- Global Perspective: Looks toward the broadest possible view of an issue or challenge; Thinks and talks in global and network terms; Understands the position of the organization within a global, network and enterprise context; Knows the impact of global trends on the organization.
- Being Resilient: Is confident under pressure; Handles and manages crises effectively; Maintains a positive attitude despite adversity; Bounces back from setbacks; Grows from hardships and negative experiences.
About Commonwealth Serum Laboratories
Sourced by ZipRecruiter
Commonwealth Serum Laboratories (CSL) is a global leader in biotechnology, based in King of Prussia, Pennsylvania. The company originates from Australia, founded in 1916 by the Australian government to service the country’s health needs. Since then, CSL has expanded operations to become a multinational specialty biotechnology company that researches, develops, and manufactures vaccines and plasma protein biotherapies. Their mission is underpinned by focused, patient-driven values. Our commitment to saving lives and protecting people's health by providing safe and effective products is a testament to the difference we are making. One of their considerate achievements includes establishing one of the largest influenza vaccine providers in the world through their brand Seqirus.
Industry
Scientific research and development services
Company size
10,000+ Employees
Headquarters location
King of Prussia, PA, US