Noven Pharmaceuticals is a leading pharmaceutical company committed to delivering innovative healthcare solutions. As we continue to expand our reach and impact, we are seeking a dynamic and analytical individual to join our team as a Sales Analyst. As a Sales Analyst reporting to the Senior Manager of Business Analytics, your primary responsibility will be to support the Commercial team. You will play a crucial role in delivering data insights, offering analytical guidance, and providing strategic operational support to the field sales team, marketing, and managed care team....

Provide technical support to manufacturing, engineering, and other departments while working on assignments that may be complex in nature. Responsible for design and implementation of manufacturing processes using considerable judgment and initiative for resolving design and implementation issues. Apply engineering principles and standards for electrical, mechanical, electromechanical, and /or optical procedures and tests in areas such as manufacturing, development, maintenance, quality, testing, and engineering projects. Design, establish specifications, construct, inspect, adjust, test, document and maintain equipment, components, devices and systems following proper procedures and instructions.  

The QC Document Reviewer is responsible for auditing all data in LIMS, Empower, laboratory worksheets, Laboratory notebooks, calibration protocols/reports and raw data archives to ensure the validity and accuracy of the data for finished product, intermedia, raw materials, components.

·         The primary purpose of this position is to lead Quality Engineering (QE) activities for product and process support including Validation of Manufacturing Processes, Cleaning Processes, and Test Methods, Qualification of Equipment, Utilities, and Facilities, Risk Management, and Annual Product Reviews. ·        

Provide technical support to manufacturing, engineering and other departments / teams by ensuring maximum equipment uptime, and addressing technical challenges. When not supporting manufacturing, technician shall perform scheduled PMs in timely manner as required by the CMMS system for work orders. Lastly, under limited supervision, performs and documents moderately complex technical functions relating to test, layout, quality control, fabrication, modification and assembly of mechanical equipment and/or components. 

Provide technical support to manufacturing, engineering and other departments / teams by ensuring maximum equipment uptime, and addressing technical challenges. When not supporting manufacturing, technician shall perform scheduled PMs in timely manner as required by the CMMS system for work orders. Lastly, under limited supervision, performs and documents moderately complex technical functions relating to test, layout, quality control, fabrication, modification and assembly of mechanical equipment and/or components. 

Responsibilities include critical evaluation of scientific documents, regulatory support, quality control, and effective communication of complex scientific information across multidisciplinary teams. This ensures trials are conducted accurately, efficiently, and in compliance with ethical and regulatory standards. Assures adherence to international Commission on Harmonization (ICH), Good Clinical Practices (GCP), and Code of Federal Regulations (CFR). Assures compliance with institutional Standard Operating Procedures (SOPs) and Policies, protocol requirements, and institutional reporting requirements. Performance of this position requires coordination and interaction among various research teams and team members.

The Mfg Operator BC performs all the general duties and operations to manufacture the product. An operator will operate machines and handle components using prescribed standard operating procedures and cGMP guidelines to manufacture and ensure the product meets the quality requirements. The operator will complete the necessary documentation and records to maintain quality control.

Perform Quality Assurance tasks such as sampling, inspections, and tests designed to ensure manufactured products are in compliance with internal SOP’s, Safety initiatives, Company policies, FDA and DEA regulations.  Document all work performed, ensuring accuracy and thoroughness.  Inform management of any deviations from established standards/procedures.

The Mfg Operator BC performs all the general duties and operations to manufacture the product. An operator will operate machines and handle components using prescribed standard operating procedures and cGMP guidelines to manufacture and ensure the product meets the quality requirements. The operator will complete the necessary documentation and records to maintain quality control.

Responsible for overall activities related to manufacturing and packaging of potential and existing products. Operate and maintain small production equipment.  Weigh, measure and check raw materials to assure batches manufactured contain proper ingredients and quantities.  Maintain records and cleanliness in compliance with cGMP, SOP, and Safety protocols.

Seeking Metrology/Calibration Technician (entry level) to calibrate and repair test instruments in accordance with precision standards and procedures. The ideal applicant is familiar with various test and measurement processes, self-motivated, a team player, and has a strong commitment to continuous improvement.

Directs and coordinates the packaging and or cartooning operation in accordance with Noven Pharmaceuticals Inc. SOPs and cGMP standards. The Lead Manufacturing Operator will set up, operate and change over packaging and or cartooning production equipment on the shift to which they are assigned. An LMO will assure that quality and documentation standards are maintained to ensure product compliance.

Directs and coordinates the packaging and or cartooning operation in accordance with Noven Pharmaceuticals Inc. SOPs and cGMP standards. The Lead Manufacturing Operator will set up, operate and change over packaging and or cartooning production equipment on the shift to which they are assigned. An LMO will assure that quality and documentation standards are maintained to ensure product compliance.

Responsible for overall activities related to manufacturing and packaging of potential and existing products. Operate and maintain small production equipment.  Weigh, measure and check raw materials to assure batches manufactured contain proper ingredients and quantities.  Maintain records and cleanliness in compliance with cGMP, SOP, and Safety protocols.

Responsible for overall activities related to manufacturing and packaging of potential and existing products. Operate and maintain small production equipment.  Weigh, measure and check raw materials to assure batches manufactured contain proper ingredients and quantities.  Maintain records and cleanliness in compliance with cGMP, SOP, and Safety protocols.

Responsible for overall activities related to manufacturing and packaging of potential and existing products. Operate and maintain small production equipment.  Weigh, measure and check raw materials to assure batches manufactured contain proper ingredients and quantities.  Maintain records and cleanliness in compliance with cGMP, SOP, and Safety protocols.

Responsible for overall activities related to manufacturing and packaging of potential and existing products. Operate and maintain small production equipment.  Weigh, measure and check raw materials to assure batches manufactured contain proper ingredients and quantities.  Maintain records and cleanliness in compliance with cGMP, SOP, and Safety protocols.

Responsible for overall activities related to manufacturing and packaging of potential and existing products. Operate and maintain small production equipment.  Weigh, measure and check raw materials to assure batches manufactured contain proper ingredients and quantities.  Maintain records and cleanliness in compliance with cGMP, SOP, and Safety protocols.

Responsible for overall activities related to manufacturing and packaging of potential and existing products. Operate and maintain small production equipment.  Weigh, measure and check raw materials to assure batches manufactured contain proper ingredients and quantities.  Maintain records and cleanliness in compliance with cGMP, SOP, and Safety protocols.