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.

The Control Electrician II is responsible for maintaining and supporting the electrical and control systems for all manufacturing equipment, utilities, and facilities to ensure the safe and efficient production of quality products.

The Associate Director of Automation Engineering is responsible for managing a team of automation engineers and supporting contractors to ensure operations performance for various manufacturing, quality, and research automated systems.

The Principal Manufacturing Engineer plays a critical leadership role in supporting and advancing manufacturing operations, with a strong emphasis on sterile/aseptic filling equipment and pharmaceutical manufacturing processes.

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 Production Supervisor supports the timely manufacturing of parenteral products in an aseptic environment according to Current Good Manufacturing Practice (cGMP).

The HVAC Mechanic II performs a wide range of tasks related to the construction, installation, maintenance, and repair of heating, ventilation, air conditioning, and refrigeration (HVAC/R) systems within the facility. In addition to core mechanical responsibilities, this role supports broader physical plant operations, including inspections, diagnostics, and preventive maintenance of building systems and production support equipment. The HVAC Mechanic II demonstrates advanced troubleshooting skills, works independently on moderately complex tasks, and may provide guidance to junior technicians as needed. Responsibilities may extend into other skilled trade areas such as electrical work, plumbing, sheet metal, welding, and general maintenance. The mechanic is expected to complete work orders and PMs on schedule, maintain accurate records, and ensure compliance with safety and regulatory standards. This position collaborates with cross-functional teams, attends meetings or committee assignments when required, and may be called upon to work overtime based on operational needs. The HVAC Mechanic II plays a critical role in sustaining a safe, comfortable, and compliant environment that supports manufacturing and facility operations.

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.

The Microbiologist I is responsible for performing microbiological testing and quality activities to support product production, environmental monitoring, and product release in a pharmaceutical manufacturing environment. This role ensures compliance with regulatory requirements and company standards by conducting microbiological assays, analyzing trends, and accurately documenting and reporting results. The QC Microbiologist I collaborates with cross-functional teams to identify potential microbiological risks, troubleshoot deviations, and contribute to continuous improvement initiatives to maintain product quality and patient safety.

Curia provides global contract research and manufacturing services to the pharmaceutical and biotechnology industries. Join our talented workforce, where a commitment to excellence and a customer focused attitude is everything. We pursue excellence because our work has the power to improve patients’ lives with the pharmaceuticals we develop and manufacture.

The Mechanical Equipment Engineer will work in supporting manufacturing operations both on the manufacturing floor and off, spending time within the manufacturing operations is required and will be a priority at times.

The Warehouse Operations falls within the Materials Management department. The Materials Management department effectively and efficiently directs supply chain functions to ensure that corporate manufacturing and quality goals for manufacturing operations are met. Materials Management department consist of managing customer order processing, materials planning, procurement, inventory control, warehousing, shipping and receiving operations. The Material Handler will perform efficient warehouse operation duties to support Manufacturing operations, receive incoming material, deliver production components and supplies, transport materials, stage materials, and issue materials in Ross ERP against work orders, bin replenishment and shipping activities.

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 Quality Program Manager II is a key member of the quality management team, responsible for ensuring the effective execution of quality programs within the framework of cGMP regulations. This mid-level role interfaces with internal and external stakeholders, including CURIA-Albuquerque customers, to manage quality-related activities, resolve issues, and facilitate batch release processes in accordance with customer and regulatory requirements.

The Aseptic Core Monitor (ACM) I role is an intermediate level role. The ACM I partners with manufacturing to provide support in the aseptic process oversite and tier one decision making activities. A successful candidate will demonstrate skills in intrapersonal communication, conflict resolution, critical thinking, decision making and the ability to break down complex concepts and teach them to others. The ACM I must communicate effectively during collaborations with production partners and escalate urgently to facilitate path forward decisions. The ACM I will work collaboratively on a routine basis with management, front line manufacturing/support group technicians and with senior MQA OTF team members.

Curia provides global contract research and manufacturing services to the pharmaceutical and biotechnology industries. The EM Analyst performs microbiological activities in support of production. The EM Analyst performs environmental monitoring of the cleanrooms for microbial and particulate counts. Directs and coordinates personnel sampling and certification in a cleanroom setting. Performs all non-routine sample collection in support of SOP or investigation requirements.

The Clinical Lab Assistant Phlebotomist is able to work independently and with minimal supervision and/or oversight. Successful candidates have the experience and skillset to perform one or more identified modalities. Compensation is dependent on the number of modalities performed. Candidates without experience may be considered for a paid apprenticeship level. Regular in-person attendance during scheduled work hours is essential.

The Clinical Lab Assistant Phlebotomist is able to work independently and with minimal supervision and/or oversight. Successful candidates have the experience and skillset to perform one or more identified modalities. Compensation is dependent on the number of modalities performed. Candidates without experience may be considered for a paid apprenticeship level. Regular in-person attendance during scheduled work hours is essential.

Under general supervision, performs waived, moderate or high complexity laboratory tests for the purpose of diagnosis and treatment of disease. Performs maintenance, basic troubleshooting and repairs of laboratory equipment. Runs and evaluates quality control testing to ensure equipment is functional prior to patient testing. May assist with the implementation and oversight of waived point of care testing. Staff in this job description meet the qualifications for designation as “Testing Personnel” for moderate and high complexity testing under CLIA regulations.

Perform a variety of histology laboratory functions, which include processing of specimens, embedding, microtomy, H&E staining and slide distribution. Produce quality tissue processing and histologic specimens to the expectations of pathologists and clients.