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Curia Aseptic Core Monitor in Albuquerque, New Mexico

Summary:

Curia provides global contract research and manufacturing services to the pharmaceutical and biotechnology industries. The Aseptic Core Monitor (Albuquerque, NM) will oversee all activities in the aseptic environment to ensure continual compliance with cGMP and provide mentoring on aseptic techniques for all aseptic personnel. This position requires expertise in all aspects of aseptic manufacturing of the sterile product, the ability to work hands-on, strong leadership skills, and the ability to collaborate in a cross-functional environment. The individual will work closely with all departments in the manufacturing environment and reports metrics to site management regularly. 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 patient’s lives with the pharmaceuticals we develop and manufacture.

Essential Duties and Responsibilities:

  • Perform daily visual audits of aseptic behavior inside the core during fills, lyophilize loading/unloading, and sanitization processes. Communicate openly to all personnel in the aseptic core to provide feedback and mentoring regarding observed performance. Take immediate action when non-compliance and/or undesired behavior by personnel in the facility is observed.

  • Provide corrective action training based on visual audits by providing immediate feedback. Partner with Operations/Quality/Training Leadership to make recommendations for enhancements to aseptic processes. Complete daily inspections of the physical conditions of the aseptic core.

  • Review the aseptic technique associated with media fills and help complete documentation. Presence in the Aseptic Core is required during all manufacturing events. Responsible for training personnel in Aseptic Techniques and processes.

  • Reports metrics and trends to site management regularly. Assumes additional duties and responsibilities as assigned.

Supervisory Responsibilities:

This job has no supervisory responsibilities

Education and/or Experience

BS, preferably in Microbiology or a related field or equivalent experience with less than three (3) years of previous professional experience. The ability to gown and work daily in an aseptic manufacturing environment. Proficient in Microsoft Excel, Word, and PowerPoint. Basic quality tools (i.e. Pareto charts, histograms, cause-and-effect, root cause analysis). Industrial GMP experience in an FDA-regulated pharmaceutical environment. Aseptic Processing experience, including proficiency in Aseptic Gowning qualifications.

Language/Communication Skills

Ability to read, analyze and interpret professional journals, technical procedures, and governmental regulations. Strong written and verbal communication and presentation skills including the ability to independently write develop and write procedures.

Mathematical Skills

Ability to calculate formulas and amounts such as concentration, percentage, area, volume, and proportion. Ability to apply the mathematical concepts from algebra and geometry.

Reasoning Ability

Ability to solve problems with a variety of variables using experience. Ability to interpret instructions furnished in written, oral, diagram, or schedule form.

Other Qualifications:

Must pass a background check

Must pass a drug screen

Physical Demands

While performing the duties of this job, the employee is regularly required to sit; use hands to manipulate, handle, and feel; and be able to talk and hear. The employee frequently is required to reach with hands and arms. The employee is required to stand; walk, and occasionally required to climb or balance; stoop, kneel, crouch, or crawl. The employee must occasionally lift and/or move up to 10 pounds. Specific vision abilities required by this job include close vision, and the ability to adjust focus.

Work Environment

While performing the duties of this job, the employee is occasionally exposed to moving mechanical parts. The noise level in the work environment is usually quiet.

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.

Note

This job description in no way states or implies that these are the only duties to be performed by the employee(s) incumbent in this position. Employees will be required to follow any other job-related instructions and to perform any other job-related duties requested by any person authorized to give instructions or assignments. All duties and responsibilities are essential functions and requirements and are subject to possible modification to reasonably accommodate individuals with disabilities. To perform this job successfully, the incumbents will possess the skills, aptitudes, and abilities to perform each duty proficiently. Some requirements may exclude individuals who pose a direct threat or significant risk to the health or safety of themselves or others. The requirements listed in this document are the minimum levels of knowledge, skills, or abilities. This document does not create an employment contract, implied or otherwise, other than an “at-will” relationship.

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