- Novo Nordisk Inc. (West Lebanon, IN)
- …is a process engineer who specializes in the cleaning and sterilization of GMP pharmaceutical manufacturing equipment in line with Novo Nordisk and FDA requirements. ... cover, frocks/coveralls, shoe covers, snood, face mask, sterile gloves, and to follow GMP processes at all times. Examples of prohibited materials in cleanroom areas… more
- Cipla (Fall River, MA)
- …Specialist is responsible for the creation and revision of new and existing GMP batch production records as well as SOP's. In this role the Documentation ... Associate degree with 4-6 years knowledge and experience of GMP documentation required. Bachelor's degree in science, biochemistry, pharmaceutical engineering,… more
- Formation Bio (New York, NY)
- …compliance with the highest standards, including Good Manufacturing Practices ( GMP ), Good Laboratory Practices (GLP), Good Clinical Practices (GCP), Good ... CSV is preferred. Strong working knowledge of global regulatory requirements, including GMP , GCP, and ICH guidelines. Expertise in Quality Management Systems (QMS).… more
- Merck & Co. (Durham, NC)
- …Troubleshooting, Field Failure Analysis, Good Manufacturing Practices ( GMP ), Maintenance Operations, Manufacturing Operations, Mechanical Engineering, Mechanical ... Maintenance, Plant Maintenance, Pneumatics, Preventive Maintenance, Production SchedulingPreferred Skills:Current Employees apply HERE Current Contingent Workers apply HERE US and Puerto Rico Residents Only:Our company is committed to inclusion, ensuring that… more
- Aequor (Davie, FL)
- …Hands-on EHS work in clinical or manufacturing environments. Familiarity with GMP , GLP, and other regulatory frameworks. Exposure to biological, chemical, or ... radiological safety protocols. Industrial hygiene experience is a must more
- Aequor (Tampa, FL)
- …on SOPs to remain current for job requirements, logbook entries and GMP documentation. Attend applicable meetings, discussions, etc., in support of these projects ... to meet the Production Schedule. Participate in safety processes and meetings as applicable. Maintain a positive, professional and confidential relationship with sponsors. Comply with all state and federal regulatory requirements and guidelines. Other… more
- Cipla (Fall River, MA)
- …Minimum of three (3) years' experience in quality assurance in a GMP pharmaceutical manufacturing operation and work environment. Experience in MDI preferred. ... KNOWLEDGE, SKILLS, AND ABILITIES Proficient user of personal computer hardware and software applications such as Microsoft Office tools, SAP, and other business applications. Must be able to influence decision-making and facilitate completion of work toward… more
- Aptyx (Charlotte, NC)
- …skills Preferred: Experience in a regulated environment (FDA, ISO 13485, GMP ) Medical device, electronics assembly, or R&D lab environment experience Knowledge ... of basic engineering parts, components, or manufacturing processes Physical Requirements Ability to regularly lift up to 30 lbs Standing, walking, bending, and moderate physical activity required in lab/warehouse environments more
- Merck & Co. (Rahway, NJ)
- …Products, Cross-Functional Teamwork, Deviation Management, Good Manufacturing Practices ( GMP ), Leadership, Manufacturing Scale-Up, New Product Introduction Process, ... Packaging Engineering, Process Optimization, Product Packaging Design, Project Leadership, Risk Management, Root Cause Analysis (RCA), Technical Leadership, Technical ProjectsPreferred Skills: Current Employees apply HERE Current Contingent Workers apply HERE… more
- Cipla (Hauppauge, NY)
- …closely working with QA department. Picks materials from Released inventory following GMP rules as required per production schedule, pick list, or production record ... requirement. Make the necessary documentation entries Deliver materials to specified locations using PIT. Load outbound freight as specified in BOL's after confirming material or production descriptions, lot numbers, count and quantities using PIT. Perform… more
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