Jobs in the United States

25+ jobs

Group jobs by employerEmail me new jobs Save this search

Added just now
Civil Engineer Intern
Aurora Tech Services
San Antonio, TX
Work as part of a team, under the supervision of a Team Lead or Project Manager.
Added just now
GC
Water Resources Market Leader
Geosyntec Consultant
Lakewood, CO
- $142,540 to $199,555 USD / year
…leader, you will be responsible for a combination of technical project execution, client relationship management and water resource subject matter expertise, task and team leadership, while…
Added just now
IC
Assistant Project Manager Intern (Summer 2027) - National Travel
Interstates Companie
Fort Collins, CO
- $31,533 USD / year
As an Assistant Project Manager at Interstates, you'll work closely with our field crews to keep projects on track and ensure we deliver excellent work to clients, all while taking on some…
Added just now
IC
Project Manager - Manufacturing
Interstates Companie
Fort Collins, CO
- $31,533 USD / year
We are looking for the future leaders on our Interstates Project Management team. At Interstates, we specialize in Electrical Construction, Engineering, Instrumentation, and Automation.…
Added just now
SC
Project Manager - Power Generation
Stanley Consultants
Denver, CO
- $40,123 USD / year
Job Title - Project Manager, Power GenerationLocation - Austin, TX | Chicago, IL | Denver, CO (Centennial) | Muscatine, IA | or Remote, USJob Type - Hybrid Requisition ID - 11399
Added just now
SC
Senior Project Manager - Nuclear
Stanley Consultants
Denver, CO
- $40,123 USD / year
Job Title - Senior Project Manager, NuclearLocation - Austin, TX | Chicago, IL | Denver, CO (Centennial) | Muscatine, IA | or Remote, USJob Type - Hybrid Requisition ID - 11401
Added just now
SC
Senior Project Manager - Power Generation
Stanley Consultants
Denver, CO
- $40,123 USD / year
Job Title - Senior Project Manager, Power GenerationLocation - Austin, TX | Chicago, IL | Denver, CO (Centennial) | Muscatine, IA | or Remote, USJob Type - Hybrid Requisition ID - 11400
Added just now
UO
Business Services Professional - 1.0 FTE
University of Colorado Denver
Aurora, CO
- $56,995 to $76,374 USD / year
Hybrid - this role is eligible for a hybrid schedule of 3 days per week on campus and as needed for in-person meetings
Added just now
W
ASSOCIATE ENGINEER
WELLS
Brighton, CO
- $31,533 USD / year
Under the direct supervision of a Senior Engineer, Engineer, or the Engineering Manager, the Associate Engineer assists in the design of precast structures and supports project teams to…
Added just now
WR
Utah Watershed Resilience Manager
World Resources Institute
Denver, CO
- $40,123 USD / year
Working closely with WRI's Research & Project Development Manager, Utah Watershed Coordinator, and the broader U.S. Forests and Water team, the Manager will lead complex multi-partner…
Added just now
TC
VDC Manager - Self Perfom Concrete
Turner Construction
Denver, CO
- $115,000 to $178,000 USD / year
…preconstruction, engineering, and field installation of VDC project…
Added just now
J
Labs and Residencies Manager
Remote, United States
- $150,000 to $165,000 USD / year
The Labs and Residencies Manager will build, scale, and oversee our labs, residencies, and future educational initiatives, acting as a key ambassador to build meaningful relationships with…
Added 1 min ago
Senior AV Project Manager
Diversified
CA
Employee must possess a valid driver’s license in their state of residence
Added 1 min ago
Senior Database Administrator
Treasure Island Resort & Casino
Welch, MN
Must have the ability to independently lift up to 25+ pounds occasionally
Added 1 min ago
Applications Manager
Treasure Island Resort & Casino
Welch, MN
Must have a good sense of balance, and be able to bend and kneel and stoop · Must have the ability to independently lift up to 25+ pounds occasionally
Added 1 min ago
K
Project Manager I
Kforce
Charlotte, NC
- $56 to $66 USD / hour
A client with Kforce is seeking a Project Manager I to join their team in Charlotte, NC. This role will be responsible for independently leading small to medium Finance and Actuarial…
Added 1 min ago
K
Tax Manager
Kforce
Quincy, MA
- $150,000 to $200,000 USD / year
Active CPA license required
Added 1 min ago
Senior Manager, Aviation Technical Consultant - Remote US
ICF
Reston, VA
MUST HAVE Requirements- · Must have valid U.S
Added 2 mins ago
IT Technical Director / System Architect Subject Matter Expert (SME)
Quantum Sky
Aurora, CO
…coordinated automation and DevOps improvement effort across development, infrastructure, database, and cybersecurity teams, reducing manual work, improving release reliability, and…
Added 2 mins ago
Process Automation Engineer - Models (EE26139)
TMEIC Corporation Americas
Roanoke, VA
· Collaborate with project engineering team to ensure inter-operation of software modules into overall project
Added 2 mins ago
Process Automation Engineer - L2 (EE26140)
TMEIC Corporation Americas
Roanoke, VA
Customize and test project-specific control and automation software for PC, PLC, and drive based industrial systems meeting project schedules
Added 2 mins ago
Analyst - Bus System Dvlmpt
Ally Bank
Detroit, MI
Hybrid roles are generally expected to be in the office a certain number of days per week as indicated by your manager
Added 2 mins ago
Manager, Brand Value Chain New Product Launch - Too Faced
Estée Lauder Companies
NY · New York
Must possess the ability to multi-task, establish priorities and yet be flexible in an ever-changing environment
Added 3 mins ago
PW
Project Engineer III
Prince William Water
Woodbridge, VA
- $55.11 to $72.32 USD / hour
Must possess and maintain a valid driver’s license consistent with Prince William Water policy requirements
Added 3 mins ago
Pre-Construction and Design Manager
National Church Residences
Columbus, OH
As Pre-Construction and Design Manager, you are responsible for leading pre-construction efforts on a development pipeline valued in excess of $50 million. This position is the Owner’s lead…

CURIA

Quality Program Manager

Albuquerque, NM, United States

Apply on hcug.fa.us2.oraclecloud.com About employer

Applications open in a new tab.

Job details

Posting language: English
Posted: Nov 13, 2026

Original job description

Quality Program Manager, NPI in Albuquerque, NM Build your future at Curia, where our work has the power to save lives Curia is a global contract development and manufacturing organization (CDMO) with over 30 years of experience partnering with pharmaceutical and biotech companies to provide life-saving treatments to patients. At Curia, we are on a mission to advance our customers’ therapies from curiosity to cure and ultimately to improve patients’ lives. We proudly offer

Generous benefit options (eligible first day of employment)
Paid training, vacation and holidays (vacation accrual begins on first day of employment)
Career advancement opportunities
Education reimbursement
401K program with matching contributions
Learning platform
And more!

The Quality Program Manager serves as the primary customer-facing Quality representative for assigned client programs at Curia's Albuquerque sterile manufacturing facility. Acting as the Quality counterpart to Project Management, this role provides strategic oversight and coordination of quality activities associated with New Product Introduction (NPI), technology transfer, process validation, commercialization, and lifecycle management of sterile pharmaceutical products. The position serves as the primary liaison between customers and the Quality organization, ensuring customer expectations, regulatory requirements, quality agreements, and site quality systems are effectively integrated throughout the product lifecycle. The role works closely with Project Management, Manufacturing, Quality Control, Technical Services, Validation, Regulatory Affairs, Supply Chain, and Engineering to identify and mitigate quality and compliance risks while supporting successful execution of customer programs. This position requires extensive experience in sterile pharmaceutical manufacturing, strong customer relationship management skills and the ability to influence cross-functional teams in a complex CDMO environment.

Essential Duties and Responsibilities:

Customer Quality Relationship Management

Serve as the primary Quality point of contact for assigned customer programs.
Develop and maintain strong working relationships with Customer Quality, Technical Operations, Regulatory and Supply Chain representatives.
Partner with Project Management in customer governance meetings, project reviews and escalation discussions to provide quality perspective, compliance guidance and risk assessments.
Lead customer discussions involving quality systems, investigations, change controls, validation activities, product quality concerns and regulatory compliance matters.
Ensure customer notification requirements are fulfilled in accordance with Quality Agreements and regulatory expectations.
Support customer audits, site visits, due diligence assessments and quality-related business discussions. New Product Introduction and Technology Transfer
Provide Quality oversight and strategic guidance for New Product Introduction (NPI), technology transfer, and commercialization activities.
Participate in project planning activities to ensure appropriate quality support and risk management strategies are established.
Coordinate quality deliverables required to support product transfers, process validation, analytical method transfers, cleaning validation and commercial launch activities.
Assess quality and compliance risks associated with new products, manufacturing processes, facilities, equipment and analytical methods.
Provide Quality input into transfer assessments, validation strategies and product control strategies.
Ensure quality requirements are appropriately incorporated into project execution plans and timelines. Quality Systems Coordination
Coordinate quality support activities impacting assigned customer programs, including:
Deviations and investigations
Corrective and Preventive Actions (CAPAs)
Change controls
Risk assessments
Product impact assessments
Validation activities
Customer notifications
Product complaints
Annual Product Reviews / Product Quality Reviews
Regulatory commitments
Facilitate cross-functional discussions to ensure timely resolution of quality issues and customer concerns.
Monitor quality system performance and communicate issues that may impact project milestones, product quality, regulatory compliance or customer commitments. Compliance and Regulatory Support
Provide guidance on applicable FDA, EMA, Health Canada, ICH, and global cGMP requirements related to sterile pharmaceutical manufacturing.
Support regulatory inspections, customer audits and remediation activities related to assigned programs.
Evaluate quality and compliance risks and recommend appropriate mitigation strategies.
Ensure activities supporting customer programs are conducted in accordance with internal procedures, regulatory requirements and approved Quality Agreements. Cross Functional Program Support
Act as the Quality counterpart to PMO, ensuring quality activities remain aligned with overall program objectives and timelines.
Collaborate with Manufacturing, QC, Validation, Technical Services, Regulatory Affairs, Supply Chain, Engineering and Project Management to support successful program execution.
Escalate quality risks, compliance concerns and resource constraints that may impact project deliverables.
Provide leadership and coordination during issue resolution activities involving quality-related customer concerns. Continuous Improvement
Identify opportunities to improve NPI processes, technology transfer activities, customer-facing quality systems and cross-functional collaboration.
Drive standardization and best practices for Quality support of customer programs.
Support development and reporting of quality performance metrics associated with customer projects and new product introductions.
Read/interpret SOPs to ensure compliance
Maintain up to date trainings
Other duties as assigned

Education & Experience:

Required

Bachelor’s degree in chemistry, Biology, Microbiology, Engineering, Pharmaceutical Sciences or related scientific discipline.
Minimum 10-15 years of experience within the pharmaceutical, biotechnology or CDMO industry.
Minimum 8 years of Quality Assurance experience supporting sterile pharmaceutical manufacturing.
Demonstrated experience supporting New Product Introduction, technology transfer, validation and commercialization programs.
Experience serving as a customer-facing Quality representative within a GMP-regulated environment.
Strong knowledge of aseptic processing, sterile manufacturing, quality systems and global regulatory requirements.
Experience supporting sterile injectable products through clinical and commercial lifecycle stages.
Working knowledge of aseptic processing, contamination control strategies, process validation, cleaning validation, environmental monitoring and microbiological controls.
Experience supporting technology transfers, process performance qualification (PPQ), and New Product Introduction (NPI) programs.
Familiarity with FDA, EMA, Health Canada, MHRA, and ICH expectations applicable to sterile drug product manufacturing. Preferred
Advanced degree in a scientific or engineering discipline.
Prior experience in a sterile injectable CDMO environment.
Experience supporting FDA, EMA and Health Canada inspections.
PMP, ASQ, RAC or equivalent professional certification.

Supervisory Responsibilities:

This position does not have direct personnel management responsibility; however, the incumbent is expected to provide leadership and coordination across cross-functional teams supporting customer programs, New Product Introduction (NPI), technology transfer, validation and commercial manufacturing activities. The position may provide mentoring, guidance and technical direction to Quality personnel and project team members.

Other Skills and Abilities:

Fosters a collaborative and positive work environment
Champions change
Promotes a safe and healthy work environment by actively identifying and addressing potential hazards, following established safety protocols, participating in safety training programs, and fostering a culture of awareness and responsibility among team members.
Demonstrates strong attention to detail
Ability to analyze complex technical, quality, operational and project-related information and apply risk-based decision-making principles. Ability to interpret quality metrics, statistical trending, validation data, process performance data and compliance information to identify risks and support business decisions.

Other Qualifications:

Must pass a background check Must pass a drug screen May be required to pass Occupational Health Screening

Education, experience, location and tenure may be considered along with internal equity when job offers are extended. We do not accept unsolicited assistance from any headhunters or recruitment firms for any of our job openings. All resumes or profiles submitted by search firms to any employee at Curia, in any form without a valid, signed search agreement by an authorized signatory in place for the specific position, approved by Talent Acquisition, will be deemed the sole property of Curia. No fee will be paid in the event the candidate is hired by Curia because of the unsolicited referral.

All interested applicants must apply online. Please be aware of scammers. Curia will only send offer letters and requests for sensitive personal information from a curiaglobal.com email address. Curia is an Equal Opportunity Employer. All qualified applicants will receive consideration for employment without regard to race, color, religion, sex, sexual orientation, gender identity, national origin, or protected veteran status and will not be discriminated against on the basis of disability. Curia is an E-Verify employer.

Apply on hcug.fa.us2.oraclecloud.com About employer

More about this job

Skills

Regulatory affairs
Supply chain management
Pharmaceutical processes
Project management
Regulatory compliance
Quality control systems
Risk management
Cleaning
Manufacturing processes
Manage quality
Inspection
Leadership
Process improvement
Collaboration
Reporting
Biotechnology
Quality assurance
Good manufacturing practices
PMP
Personnel management
Coaching
Attention to detail
Decision making
Recruitment

Report this job

Work requirements

Jobs in the United States