The Senior Program Manager III is responsible for managing the successful technical transfer of client programs and products to Curia. This includes the management of a client-Curia cross functional team that manages all aspects of client program including, but not limited to, scheduling, logistics, regulatory strategies, equipment procurement, validation strategy, and all other items as necessary to complete technical transfer of the client’s program.

The Chemist III provides advanced analytical testing and technical leadership within the Chemistry Department supporting internal manufacturing and external customer programs. The laboratory performs testing of raw materials, in-process samples, finished products, stability samples, plant water, and particulates to support manufacturing and quality operations. This role independently performs and troubleshoots complex analytical testing using a variety of laboratory instrumentation, ensuring compliance with approved methods, specifications, and regulatory requirements. The Chemist III interprets and evaluates data, leads or supports method transfers, validations, investigations, and new product onboarding, and ensures accuracy and integrity of all analytical documentation. In addition, the Chemist III serves as a technical resource, providing mentorship and training to junior staff, authoring and reviewing technical documents, and collaborating cross-functionally with Quality, Manufacturing, Validation, Engineering, and customers. The role also supports continuous improvement initiatives, regulatory inspections, and maintains a state of GMP/GLP compliance and inspection readiness.

The Manager, Manufacturing Quality Assurance (MQA) is responsible for directing and overseeing all MQA activities to ensure consistent quality support of daily manufacturing operations and product lot release. This role serves as the primary Quality liaison for internal departments, providing guidance on product, process, and material issues while ensuring adherence to regulatory, corporate, and customer quality standards. Key responsibilities include in-process and final product inspections, on-the-floor batch record review, 24/7 QA oversight, and support for validation, change control, and deviation investigations. The MQA Manager leads the hiring, training, and development of MQA staff and drives continuous improvement initiatives aligned with current regulations and best industry practices. Additionally, the role supports strategic and global quality projects, fosters cross-functional collaboration, and ensures that all manufacturing operations consistently produce safe, effective, and high-quality products.

The Associate Director of Training and Development will manage Albuquerque’s centralized hands-on training function called Sterile University. Sterile University helps attract, train and retain talent by providing development paths for technicians, reinforcing our shared culture tied to values & mission, and designing engaging on-time training. This position is responsible for the oversight and effective management of New Hire Orientation. The position is also responsible for coordinating and managing site-wide training programs to ensure we have a skilled workforce that can meet safety, quality, and production targets. The Associate Director will manage a team of training specialists, some of which are aligned to manufacturing shifts. They will set high performance expectations, provide ongoing feedback and professional development opportunities for team members, and foster a culture of continuous learning and talent growth within the organization. Some classroom facilitation is required.

The Production Support Operator ensures compliance with cGMP standards, maintains accurate and thorough documentation, and contributes to ongoing training and process improvement efforts to optimize production efficiency and product quality. Responsibilities are comprised of supporting the timely manufacturing of parenteral products, including vial preparation, fill line operation, lyophilizer loading/unloading, and vial sealing, all conducted in an aseptic environment according to Current Good Manufacturing Practice (cGMP). The role encompasses setting up, operating, sanitizing, and sterilizing equipment and manufacturing areas within a cleanroom setting. Key tasks include preparing, washing, and sterilizing vials, performing batch calculations and formulations, and ensuring compliance with all relevant regulations and procedures. The operator maintains current good documentation practices (cGDP) for all activities and actively participates in training and continuous improvement initiatives to enhance production processes and efficiency. Responsibilities also extend to sanitizing aseptic and controlled areas using specialized solutions and equipment, adhering to sanitization protocols during sterile processing, and strictly following Standard Operating Procedures (SOPs) for all sanitization and documentation tasks. Additionally, the role involves the preparation, sterilization, cleaning, and decontamination of both dedicated and non-dedicated manufacturing equipment in a cleanroom environment. The operator handles the compounding or formulation of drug solutions, using costly raw materials and hazardous chemicals, while adhering to safety protocols and wearing appropriate personal protective equipment.

The Manufacturing Engineering Technician provides technical and operational support for the manufacture of sterile parenteral products in a controlled and aseptic environment. This role supports manufacturing operations by ensuring compliance with current Good Manufacturing Practices (cGMP), company procedures, and regulatory requirements while promoting safe, efficient, and compliant production activities. The Manufacturing Engineering Technician partners closely with Manufacturing Engineering, Quality, and Operations personnel to support equipment readiness, manufacturing processes, troubleshooting efforts, personnel development, and continuous improvement initiatives. This position requires strong technical aptitude, attention to detail, and the ability to maintain a consistent presence within manufacturing operations to support business needs.

The Manager of Analytical Chemistry is responsible for overseeing all operations within the Analytical Chemistry Laboratory. This role encompasses a wide range of duties, including personnel management (hiring, conducting performance reviews, managing performance, scheduling, etc.), budget preparation and management, and ensuring the lab is audit-ready for both regulatory bodies and customers. The Manager will also be responsible for developing and maintaining departmental metrics, representing the department in various internal and external meetings, and collaborating with both internal stakeholders and external customers to deliver exceptional service. Additionally, this position involves fostering a culture of continuous improvement, ensuring compliance with Good Laboratory Practices (GLP) and Good Manufacturing Practices (GMP), and leading initiatives to enhance laboratory efficiency and effectiveness.

The Chemist III provides advanced analytical testing and technical leadership within the Chemistry Department supporting internal manufacturing and external customer programs. The laboratory performs testing of raw materials, in-process samples, finished products, stability samples, plant water, and particulates to support manufacturing and quality operations. This role independently performs and troubleshoots complex analytical testing using a variety of laboratory instrumentation, ensuring compliance with approved methods, specifications, and regulatory requirements. The Chemist III interprets and evaluates data, leads or supports method transfers, validations, investigations, and new product onboarding, and ensures accuracy and integrity of all analytical documentation. In addition, the Chemist III serves as a technical resource, providing mentorship and training to junior staff, authoring and reviewing technical documents, and collaborating cross-functionally with Quality, Manufacturing, Validation, Engineering, and customers. The role also supports continuous improvement initiatives, regulatory inspections, and maintains a state of GMP/GLP compliance and inspection readiness.

The Manager of Quality Compliance plays a critical leadership role within the Curia Albuquerque team, overseeing key elements of the Quality System to ensure sustained regulatory compliance and continuous improvement. This role is responsible for leading internal and external audits, managing Annual Product Quality Reviews (APQRs), and supporting customer and regulatory interactions. The Manager ensures alignment with Curia Global Standards and applicable regulatory guidelines, including ICH Q10, FDA 21 CFR Parts 210/211, EMA, and other international health authorities. The position leads the inspection readiness program, facilitates gap assessments, and drives the execution of remediation plans to address audit findings. This individual provides strategic guidance to site teams on Quality System improvements, supports Quality Improvement Plans (QIPs), and utilizes metrics to monitor trends and identify areas requiring action. The role requires strong cross-functional collaboration and the ability to lead compliance initiatives across departments to meet quality objectives and regulatory expectations.

The Validation Specialist III is a senior-level professional responsible for leading the development, review, and execution of complex validation protocols supporting manufacturing, quality, and regulatory compliance. This role provides advanced technical expertise and strategic guidance on equipment, process, system, and computer system validations in accordance with cGMP, FDA regulations, and industry standards such as GAMP. The Validation Specialist III leads cross-functional validation projects, coordinates validation activities across multiple departments, and ensures seamless integration with production and quality timelines. This role authors and approves comprehensive validation master plans, protocols, and technical reports while driving continuous improvement initiatives to optimize validation processes. Additionally, the Validation Specialist III mentors junior validation staff, supports regulatory inspections and audits, manages validation-related investigations and deviations, and collaborates with external vendors and regulatory bodies. This position plays a key role in shaping validation strategies and ensuring organizational readiness for new product introductions and regulatory submissions.

The Quality Program Management Supervisor will oversee and guide the QA batch record review and product disposition team. The supervisor is responsible for fostering strong client quality relationships and ensuring the timely review and disposition of executed batch records (clinical, commercial, and media fills). This role works closely with cross-functional teams to monitor and support the stages of the batch disposition process, including manufacturing and quality reviews, to ensure deliverables are completed on schedule to meet supply commitments. Key responsibilities include supporting the establishment, tracking, and improvement of batch record review and disposition cycle times. The role also involves coordinating shipments with the warehouse, participating in critical DEV review meetings to provide quality input, and contributing to the preparation of weekly and monthly metrics for senior leadership. Additionally, the supervisor will assist with identifying and implementing process improvements and support other QA areas as assigned by QA management.

The Microbiology Manager is responsible for overseeing the daily operations of the Microbiology laboratory and leading strategic planning for the lab and its staff. They serve as the subject matter expert on contamination control and microbiological testing of parenteral drug products. This role involves significant participation in customer and regulatory audits, new client interactions, site metrics meetings, site-wide improvement projects, budgeting, and data review and interpretation, including protocols, investigations, and lab documentation. The manager is accountable for the entire laboratory team and handles staff management duties such as performance reviews, disciplinary actions, and ensuring proper training. Operating with limited supervision, this position requires the ability to work independently as well as collaboratively on cross-functional teams.

The Process Engineer IV will execute and oversee advanced engineering functions such as process design, scale-up, and meticulous documentation control. This position will collaborate closely with cross-functional teams, including R&D, Quality Assurance, and Production, providing technical leadership and expertise to drive process improvements, enhance operational efficiency, and ensure compliance with industry standards such as cGMP and FDA regulations.

The Automation Controls Engineer II is responsible for maintaining the control and data acquisition systems of the manufacturing, packaging, and support equipment at the site, including Supervisory Control and Data Acquisition (SCADA) systems, PLC (Programmable Logic Controllers), and Human Machine Interface (HMI) devices. Provides technical review and counsel on a variety of technical issues related to his/her expertise, and constantly looks for opportunities related to efficiency, reliability, and obsolescence, to identify business opportunities aligned with the site and company goals.

The Microbiology Supervisor is responsible for overseeing the daily operations of the microbiology laboratory, including scheduling and directing the work of analysts and technicians. This role ensures compliance with cGMP requirements, company policies, and regulatory standards by coordinating microbiological testing, environmental monitoring, and laboratory studies. The Supervisor provides technical expertise, training, and guidance to laboratory staff; monitors equipment performance and laboratory supplies; and supports investigations, audits, and cross-functional initiatives. Additionally, the Microbiology Supervisor collaborates closely with the Microbiology Manager and other departments to maintain laboratory readiness, ensure data integrity, and drive continuous improvement within the microbiology function.

The Senior Principal Validation Engineer oversees Validation Contractors for the Albuquerque expansion and other key site projects. The majority of this role involves supervising relevant contractors at the Albuquerque site, including reviewing project proposals, interviewing, completing bid analysis, and selecting contractors. Responsibilities include managing projects and daily activities, overseeing validation activities, reviewing change controls, maintaining validated equipment, and updating validation documents such as the Validation Master Plan(s). Additional duties involve coordinating with departments to ensure timely completion of risk assessments, IQ, OQ, and PQ activities for new components, equipment, systems, and utilities, as well as developing and executing validation protocols for processes, equipment, utilities, and test systems. The role also supports new product introductions, equipment re-qualification schedules, and ensuring plant readiness post-shutdowns. The Senior Principal Validation Engineer will work with engineering, contractors, and facilities personnel to ensure proper system installation and operation, providing technical support for validated systems.

The Metrology Technician II is responsible for the calibration, maintenance, and repair of various types of measurement and test equipment (M&TE) throughout the facility to ensure accuracy and compliance with industry standards. This role involves scheduling and performing calibrations, troubleshooting instrumentation issues, and maintaining detailed calibration records. The technician will work with both analog and digital equipment, including but not limited to gauges, transducers, temperature and humidity sensors, calipers, micrometers, top-loading balances, and floor scales. Additionally, this role requires coordination with external vendors to ensure timely calibration of designated equipment by certified laboratories.

The Site Head of Quality at the Albuquerque, NM facility is responsible for establishing and maintaining the site quality system to meet the regulatory expectations and cGMP requirements for various global regions. This position’s responsibilities include leading the site Quality organization, which consists of Compliance & Quality Systems, Quality Operations (IQA, MQA and Sterility Assurance), Validation, and Quality Control by providing leadership and guidance in quality decision making. The Quality Control laboratories include both the chemistry and microbiology teams. The Site Head of Quality is also responsible for directing and providing leadership for the implementation of Curia global standards and procedures to ensure quality decisions are made conforming to highest standards and in the successful operation of the Quality Organization.

The Process Engineer IV will execute and oversee advanced engineering functions such as process design, scale-up, and meticulous documentation control. This position will collaborate closely with cross-functional teams, including R&D, Quality Assurance, and Production, providing technical leadership and expertise to drive process improvements, enhance operational efficiency, and ensure compliance with industry standards such as cGMP and FDA regulations.

The Environmental Monitoring (EM) Analyst conducts microbiological tasks to aid production, such as monitoring cleanrooms for microorganisms and particles. They manage personnel sampling and certification in a cleanroom environment and perform non-routine sample collection for Standard Operating Procedures (SOPs) or investigations.