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Project Manager Cdmo Jobs in Houston, TX (NOW HIRING)

Senior Program Manager

Spring, TX ยท On-site

$106K - $106K/yr

The Senior Program Manager will lead multiple client Process Development and GMP Manufacturing ... Science minimum required 5+ years in CDMO and GMP environment2+ years in Project ...

Extensive experience managing complex programs in biotech, pharma, or CDMO environments * Strong ... PMP or equivalent project management certification preferred * Strong problem-solving mindset with ...

Extensive experience managing complex programs in biotech, pharma, or CDMO environments * Strong ... PMP or equivalent project management certification preferred * Strong problem-solving mindset with ...

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Project Manager Cdmo information

See Houston, TX salary details

$42.5K

$92.2K

$147.5K

How much do project manager cdmo jobs pay per year?

As of Aug 22, 2026, the average yearly pay for project manager cdmo in Houston, TX is $92,212.00, according to ZipRecruiter salary data. Most workers in this role earn between $71,600.00 and $107,900.00 per year, depending on experience, location, and employer.

What is a project manager CDMO?

A Project Manager CDMO (Contract Development and Manufacturing Organization) is responsible for overseeing pharmaceutical or biotech projects outsourced to CDMOs. They coordinate between clients and internal teams to ensure timely delivery, quality, and compliance with regulatory standards. Their role includes managing project timelines, budgets, and resources, as well as communicating progress and addressing issues that may arise during drug development and manufacturing processes.

How does a project manager at a CDMO typically coordinate between clients and internal teams throughout a project lifecycle?

A Project Manager at a Contract Development and Manufacturing Organization (CDMO) acts as the central point of contact for clients and internal teams, ensuring clear communication and alignment of project goals. They regularly facilitate meetings, track project milestones, and proactively address potential issues or changes in scope. This involves close collaboration with departments such as R&D, manufacturing, quality assurance, and regulatory affairs to meet client expectations and project timelines. Effective project managers also document progress and maintain transparent reporting to both clients and internal stakeholders.

What are the key skills and qualifications needed to thrive as a project manager in a CDMO, and why are they important?

To excel as a Project Manager in a CDMO, you need a strong background in project management, life sciences, and regulatory compliance, often supported by a relevant degree and PMP certification. Familiarity with project management software (like MS Project or Smartsheet), quality management systems, and industry-specific regulations such as GMP are typically required. Outstanding organizational, communication, and stakeholder management skills help you effectively coordinate cross-functional teams and client expectations. These competencies are vital for delivering complex projects on time and within budget while maintaining regulatory standards and client satisfaction.

What cities near Houston, TX are hiring for Project Manager Cdmo jobs?

Cities near Houston, TX with the most Project Manager Cdmo job openings:

Infographic showing various Project Manager Cdmo job openings in Houston, TX as of August 2026, with employment types broken down into 100% Full Time. Highlights an 86% In-person, and 14% Remote job distribution, with an average salary of $92,212 per year, or $44.3 per hour.

Manufacturing Supervisor (Cell Therapy CDMO)

Cellipont Bioservices

The Woodlands, TX โ€ข On-site

$54K - $73K/yr

Full-time

Medical, Retirement, PTO

Re-posted 13 days ago


Job description

"Bridging Innovation to Cure

"Developing and manufacturing your cell therapies from benchtop to bedside"

Summary

Cellipont Bioservices is growing, and we are looking for a Manufacturing Supervisorย who believes in the potential bridging of client's discoveries to patient cures and who want to challenge the status quo and take Cellipont and its clients to the next level.

The Manufacturing Supervisor will provide hands-on direction for manufacturing personnel and activities. This position requires extensive technical expertise in aseptic techniques. Provide expertise in writing/reviewing SOPs, Batch Records, Deviations, CAPA's and other technical document/compliance documents as it relates to the Manufacturing Operations. The Manufacturing Supervisor is also responsible for ensuring all personnel activities are executed timely and cost effectively to ensure customer and stakeholder satisfaction. This role will also require the individual to demonstrate strong customer service capability, ability to work cross-functionally and possess strong leadership skills.

The Role

  • Oversee and schedule the manufacturing operations and personnel
  • Leads a manufacturing team to identify issues and propose adequate solutions
  • Responsible for training manufacturing personnel on the use of the Batch records, scheduling, ordering of raw materials, components and supplies, setting up production batches, and maintaining inventory
  • Ensure batches adhere to established Quality standards
  • GMP batch review and close-out with Quality Assurance group
  • Conduct interviews and provide input for hiring new manufacturing specialist.
  • Provide daily production updates to production managers, client representatives, and project managers
  • Provide guidance for continuous improvement initiatives within the Manufacturing team
  • Represent the department to clients and on cross-functional project teams
  • May operate production equipment and inspect, label, or package products
  • Work with Manufacturing, Quality, Engineering and Technology groups on issues and identifies process improvement opportunities
  • Ensure the completeness and accuracy of manufacturing documentation per approved procedures.
  • Identify and support the implementation of process efficiencies and areas for improvement
  • Ensures solutions are consistent with organization's objectives
  • Responsible for establishing performance standards, employee coaching and development, determining employee responsibilities, evaluating performance and rewarding as appropriate
  • Perform additional duties as needed

The Candidate

  • Bachelor's Degree - Life Sciences or Chemical Engineering and minimum 5 - 7 years in GMP environment with experience in GMP manufacturing operations/Cell Therapy/Human Cell Cultivation. CDMO experience preferred.
  • 3 years minimum of leadership/management experience in a GMP environment
  • Experience in writing, executing and reviewing SOPs / MBRs while maintaining proper GDP guidelines.
  • Good mechanical aptitude, familiar with general equipment associated with Cell and Gene Therapy Processing.
  • Detail oriented and highly motivated, follow oral and written instructions, communicate effectively, think logically, and thrive independently and/or in a fast-paced team environment
  • Must be proficient in Word and Excel.
  • Ability to interpret process trends and data and react appropriately to unexpected outcomes.
  • Innovative spirit, strong initiative and work ethic, and positive attitude
  • Ability to work flexible hours and inconsistent schedules as necessary to meet production demands and timelines
  • Must be available to work 2nd shift (2:00 PM โ€“ 11:00 PM), Monday through Friday, with occasional weekend or holiday support as needed

Work Environment

  • Comfortable in a fast-paced small company environment with minimal direction and able to adjust workload based upon changing priorities
  • Ability to work off-shift and extra hours as required
  • Weekends & Holidays as required

POSITION BENEFITS

  • Opportunities for career growth within an expanding team
  • Defined career path and annual performance review & feedback process
  • Cross-functional exposure to other areas of within the organization
  • Robust benefit package designed for unique Health & Wellness needs, including coverage for your furry family members
  • 401K strong employer match
  • Tuition Reimbursement
  • Employee Referral Bonuses
  • Flexible work schedules and PTO based on role/level, increasing 1 PTO day each year and paid holidays
  • Gain experience in the cutting-edge cell therapy space

"At Cellipont Bioservices, we look for candidates with an innate desire to serve. Our "family" approach ensures you will get the mentorship you need to develop a satisfying career here!"

Notice to Agency and Search Firm Representatives

Cellipont Bioservices is not accepting unsolicited resumes from agencies and/or search firms for this job posting. Resumes submitted to any Cellipont Bioservices employee by a third-party agency and/or search firm without a valid written & signed search agreement, will become the sole property of Cellipont Bioservices. No fee will be paid if a candidate is hired for this position as a result of an unsolicited agency or search firm referral.