Average salary: $128,618 /yearly
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$30 - $40 per hour
...materials, repair notes, hour-meter readings, and serial numbers.Document repairs to meet Cal-Line, manufacturer (including Bandit and CMC), customer, billing, and warranty requirements, including photos and failed-part retention when required.Communication &...SuggestedWeekly payRemote workMonday to Friday- ...it's what's inside that counts _______________________________ There’s more to CMC than our products and the buildings, structures, and roads they go into. At CMC, it’s the people inside our recycling centers, fabrication plants, manufacturing facilities, steel mills...SuggestedWork at officeLocal areaImmediate start
- ...it's what's inside that counts _______________________________ There’s more to CMC than our products and the buildings, structures, and roads they go into. At CMC, it’s the people inside our recycling centers, fabrication plants, manufacturing facilities, steel mills...SuggestedFor contractorsWork experience placementWork at officeLocal areaImmediate start
- ...drug development expertise, we are focused on accelerating meaningful medical breakthroughs. Position Overview The Director, Regulatory CMC will provide strategic leadership for global Chemistry, Manufacturing, and Controls (CMC) regulatory activities across a portfolio of...SuggestedContract work
$212.5k - $250k
...per week on‑site Employee Value Proposition: Join our dynamic and expanding mid‑size company in the role of Director for Regulatory CMC directly reporting to Executive Director, Regulatory CMC. Your expertise will play a pivotal and visible role in advancing CMC strategy...SuggestedFor contractors3 days per week$133.2k - $172.37k
...empowered to fulfil their aspirations. Join Kite and help create more tomorrows.## Job Description## The Manager, Global Regulatory CMC will support Kite’s autologous CAR T cell therapy portfolio, providing regulatory CMC leadership for global clinical development and...SuggestedFull timeWork at officeRemote workRelocationFlexible hours- ...is currently expanding its pharmaceutical division. As part of this growth, the organization is seeking a Regulatory Affairs Manager CMC to join their Regulatory team in San Francisco. This is an exciting opportunity to play a hands-on role in regulatory strategy and submissions...Suggested
$150k - $170k
...risk management, and delivery of program milestones. This role requires a strong foundation in project management with an emphasis on CMC knowledge and the ability to support Clinical Development activities as needed. The ideal candidate is a proactive, solutions-...SuggestedWork at officeLocal areaRemote work- ...Administrative Assistant, CMC Be the calm, capable center of gravity for a fast-moving Technical Operations team owning complex calendars, high-stakes logistics, and cross-functional projects for leaders who rely on you to make the day run smoothly. This role puts you...SuggestedContract workWork at officeLocal areaShift work
$133.2k - $172.37k
...Join Kite and help create more tomorrows. Job Description This is an office based/hybrid position. The Manager, Regulatory Affairs CMC is located in El Segundo, CA, Thousand Oaks, CA, Foster City, CA or Parsippany, NJ. Kite is transitioning from its current Santa Monica...SuggestedContract workWork at officeLocal areaRemote workRelocationFlexible hours$207k - $253k
The Director of Regulatory Affairs, Chemistry Manufacturing Controls (CMC) provides strategic leadership and functional ownership for global CMC regulatory activities supporting the Company’s cell therapy products and associated delivery devices from clinical development...SuggestedWork at officeRemote workRelocationWeekend work$206k - $254k
...preventative actions, deviations, and investigations. Author and review necessary technical sections in IND/IMPD/NDA supporting global CMC regulatory submissions and remain current on Health Authority guidance and expectations. Represent DS/CMC and participate in cross...SuggestedContract workTemporary workWork at officeLocal areaWork from homeShift work- Taiho Oncology, Inc. seeks a senior Director to lead global regulatory CMC activities, coordinating strategy, submissions, and approvals across US, EU, and other regions. This role partners with internal teams and external consultants to ensure compliant development and...Suggested
- Experienced Project Manager Leading cross-functional CMC activities for early-stage biopharma development programs, including process development, analytical, quality, regulatory, and supply chain functions. Primary objectives involve developing integrated project plans...Suggested3 days per week
$162.5k - $227.5k
Associate Director, CMC Project Management Vir Biotechnology, Inc. is a clinical-stage biopharmaceutical company focused on powering the immune system to transform lives by discovering and developing medicines for serious infectious diseases and cancer. Its clinical-stage...SuggestedFull timeFor contractorsWork at officeRemote workWork visa3 days per week- ...as visiting existing or new clients and promoting WuXi XDC’s services at conferences/trade shows. Responsibilities: Participate in CMC projects. Coordinate with sponsors and internal expertise to design appropriate studies to meet regulatory requirements and project’s...Contract workWork experience placementWorldwide
$175k - $215k
...Manufacturing Location: Redondo Beach Compensation: $175,000 - $215,000 / year Description As a Staff or Principal Manufacturing Engineer for CMC Applications at Impulse Space, you will own the end-to-end ceramic matrix composite manufacturing capability, from material selection...Permanent employmentFull time- Dendreon Pharmaceuticals LLC in California is seeking a Manager of Regulatory Affairs (CMC) to lead regulatory strategies for biologics, cell, and gene therapies. You will drive submissions, provide strategic guidance, and coordinate with cross-functional teams to ensure...
$159k - $207k
Key Accountabilities/Core Job Responsibilities: Organize, manage, and drive CMC strategies, plans, and deliverables for drug candidates from research, pre-IND, and first-in-human through later phases, including pivotal Phase 2/3 and NDA/MAA/BLA submissions. Manage CRO/CMO...$143.23k - $185.35k
...working and three days working onsite. Key Responsibilities Regulatory Strategy and Program Leadership Lead or support integrated global CMC regulatory strategies for both T-cell drug product and LVV, with clear differentiation between early-stage, pivotal/late-stage,...For contractorsWork at officeLocal areaRemote workRelocationFlexible hours- Enigma Search in the United States is seeking a Director, Regulatory CMC to lead global regulatory activities for small molecules and monoclonal antibodies, shaping strategies for accelerated development and successful product registrations. The role partners with CMC,...
- Neurona Therapeutics, a neuroscience-focused cell therapy company, is seeking a Senior Manager/Associate Director, CMC Project Management to lead integrated CMC planning and execution across multiple cross-functional teams supporting clinical supply, late-stage development...
$159k - $207k
...meaningful therapeutics to patients. Denali Therapeutics is seeking to recruit a leader who will be responsible for organizing and managing CMC strategies, deliverables, and timelines for Denali’s programs, including oversight of contract manufacturing organizations. As a...Contract workLocal area- Denali Therapeutics Inc. is seeking a Principal Scientist for the Large Molecule Analytical Development team to lead commercial analytical lifecycle activities. The role focuses on providing technical analytical expertise for in-country testing, method transfers, and international...
$181.62k - $211.89k
...new commercial product, and to work in a dynamic and collaborative cross functional team environment. Job Purpose The Senior Manager, CMC Analytical, is responsible for the execution and oversight of analytical development and quality control activities supporting late-...Contract workWork experience placement- The Senior CMC Consultant for Viral Vector Analytics provides key support for analytical strategy integrated with product development and launch programs . Primary accountability and focus on clinical and commercial retroviral vector analytical testing, enabling advancement...Work experience placementShift work
- Kite Pharma, Inc. is seeking a Manager, Regulatory Affairs CMC to lead regulatory submissions and lifecycle activities for LVV and cell therapy programs. This office-based/hybrid role is located in El Segundo, CA with relocation consideration to Thousand Oaks, CA, or other...Work at officeRelocation
$35 - $55.25 per hour
...Job Description Drug Development Program Manager - CMC (part time) – Pharmaceutical Industry QUICK FACTS \n Location: San Diego, CA, 92130 \n Pay range: $35.00 - $55.25 per hour \n Shifts: Part-time, 24 hours per week (3 days of your choice M-Th) \n Duration...Hourly payContract workPart timeLocal areaShift workQualStaff Resources
San Diego, CA21 days ago$181.16k - $224.72k
Associate Director, CMC Regulatory Affairs Job Category : Development - Ionis Requisition Number : IONIS004158 Posted : October 9, 2026 Full-Time Locations Showing 1 location Headquartered in Carlsbad, California, and with offices in Boston, Massachusetts, and Dublin, Ireland...Full timeRemote work- Kite Pharma, Inc. hires for a Manager, Global Regulatory CMC to lead regulatory CMC submissions and lifecycle management across global CAR‑T programs. The role requires coordinating with Technical Operations, Quality, Process Development and Regulatory teams in US, EU,...
