Manufacturing Associate

Manufacturing Associate Medix - 3.7 Baltimore, MD Job Details Contract Up to $24 an hour 19 hours ago Qualifications Machine operation Pharmaceutical regulatory compliance Safety standards in production Mid-level Industrial equipment troubleshooting Manufacturing standard operating procedures Continuous improvement Batch records Pharmaceutical plant experience Organizational skills Cleaning Quality standards in production Manufacturing maintenance 1 year Aseptic technique Cross-functional collaboration Communication skills Cross-functional communication Engineering validation Full Job Description Job Summary Seeking candidates with experience in pharmaceutical or biopharmaceutical manufacturing to support GMP production operations in a regulated environment. This role may support upstream, downstream, formulation, fill/finish, or related manufacturing activities depending on business needs. Responsibilities include operating process equipment, preparing materials, following batch records and SOPs, documenting manufacturing activities, and collaborating cross-functionally with Quality, Maintenance, Engineering, Validation, and other operational teams. Key Responsibilities Support manufacturing operations in a cGMP-regulated environment Operate, clean, and maintain manufacturing/process equipment according to SOPs Execute production activities following batch records and standard procedures Perform calculations, measurements, and documentation to ensure quality and compliance standards are met Assist with process scale-up, technical transfer, validation, engineering, or continuous improvement activities as needed Accurately complete batch records, logbooks, and production documentation Collaborate with cross-functional teams to troubleshoot production, equipment, or material issues Support preparation and staging of materials for manufacturing activities Adhere to all GMP, safety, and compliance requirements Qualifications Degree, diploma, certificate, or equivalent experience in a scientific or technical field preferred 1-3+ years of experience in pharmaceutical, biopharmaceutical, or related GMP manufacturing environments Working knowledge of cGMP regulations and manufacturing documentation practices Experience operating within a regulated production environment Strong communication, teamwork, and organizational skills Ability to follow detailed procedures and maintain accurate documentation Experience supporting upstream, downstream, formulation, fill/finish, or aseptic manufacturing operations is a plus

For California Applicants:

We will consider for employment all qualified Applicants, including those with criminal histories, in a manner consistent with the requirements of applicable federal, state and local laws, including the City of Los Angeles' Fair Chance Initiative for Hiring Ordinance (FCIHO), Los Angeles Fair Chance Ordinance for Employers (ULAC), The San Francisco Fair Chance Ordinance (FCO) , and the California Fair Chance Act (CFCA). This position is subject to a background check based on its job duties, which may include patient care, working with vulnerable populations, access to financial and confidential information, driving, working with heavy machinery, or working in a warehouse or laboratory environment. Due to these job duties, this position has a significant impact on the business operations and reputation, as well as the safety and well-being of individuals who may be cared for as part of the job position or who may interact with staff or clients.