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  • 4701 International Blvd, Wilson, NC 27893, USA ● Req #148
    Wednesday, June 29, 2022
    Job SummaryThe Distribution Technician will ship, receive, and reconcile inventory in support of manufacturing and product development activities. The Warehouse and Inventory specialist must be experienced in a cGMP manufacturing environment and have a thorough understanding of the domestic and international movement of raw materials, components, and finished product. Primary Responsibilities Responsible for packaging product for shipment to external customers and ensuring proper documentation i ... More
  • 4701 International Blvd, Wilson, NC 27893, USA ● Req #147
    Wednesday, June 29, 2022
    Job Summary   The Quality Specialist I, Chemist is responsible for supporting the operations and manufacturing process by performing routine and non-routine analytical testing and GMP review in support of the analysis of raw materials, packaging components, ancillary solutions, in-process samples, finished product method development and/or transfers, cleaning/process validations, and stability samples.   Will follow standard procedures in accordance with cGMP, GLP, DEA and company po ... More
  • 4701 International Blvd, Wilson, NC 27893, USA ● Req #143
    Wednesday, June 29, 2022
    Job Summary: The Pharmaceutical Technician will efficiently, effectively, and safely clean, set-up, and operate machinery in the encapsulation/compression manufacturing area while adhering to applicable cGMPs, SOPs, FDA, and DEA guidelines. Primary Responsibilities: Follow Master Batch Records for the manufacturing and packaging of controlled, oral solid dose (OSD) and other dosage forms when required.Prepare raw materials, blends, and bulk accountability throughout manufacturing processes ... More
  • The Pharmaceutical Process Specialist will efficiently, effectively, and safely clean, set-up, and operate machinery in the packaging area while adhering to applicable cGMPs, SOPs, FDA, and DEA guidelines. This position requires the ability to work 40 hours per week and overtime as required. Primary Responsibilities   Follow Master Batch Records for the packaging of controlled, oral solid dose (OSD) and other dosage forms when required. Prepare raw materials ... More
  • Wilson, NC, USA ● Req #145
    Tuesday, June 7, 2022
    The Pharmaceutical Process Specialist will efficiently, effectively, and safely clean, set-up, and operate machinery in the packaging area while adhering to applicable cGMPs, SOPs, FDA, and DEA guidelines. This position requires the ability to work 40 hours per week and overtime as required. Primary Responsibilities Follow Master Batch Records for the packaging of controlled, oral solid dose (OSD) and other dosage forms when required.Prepare raw materials, blends, and bulk accountability through ... More
  • Stamford, CT, USA ● Virtual ● Req #137
    Wednesday, June 1, 2022
    Job Summary:Under the direction of the Senior Manager, theManager, Corporate Procurement is responsible for supporting the direction and oversight of the sourcing, procurement, and purchasing function of Clinical R&D. The individual will develop and foster external clinical partnerships and assist in contract development, financial and contract management. This position must take a broad, high-level approach to sourcing, incorporating business and corporate objectives and maximizing vendor value ... More
  • Job SummaryThe Quality Assurance (QA) Specialist II, QA Production Support is a position on the Second Shift. The candidate must demonstrate thorough understanding, knowledge, and ability in primary discipline. The QA Specialist II, QA Production Support is responsible for performing incoming sampling of materials, support room /line clearances and provide QA input into production event resolution to assure that quality operations are in conformance to GMP requirements. Also responsible for id ... More
  • Job Summary: The Pharmaceutical Technician will efficiently, effectively, and safely clean, set-up, and operate machinery in the encapsulation/compression manufacturing area while adhering to applicable cGMPs, SOPs, FDA, and DEA guidelines. Primary Responsibilities:  Follow Master Batch Records for the manufacturing and packaging of controlled, oral solid dose (OSD) and other dosage forms when required.Prepare raw materials, blends, and bulk accountability throughout manufacturing processe ... More
  • Wilson, NC, USA ● Req #132
    Friday, May 27, 2022
    Job SummaryThe Quality Specialist I, Chemist is responsible for supporting the operations and manufacturing process by performing routine and non-routine analytical testing and GMP review in support of the analysis of raw materials, packaging components, ancillary solutions, in-process samples, finished product method development and/or transfers, cleaning/process validations, and stability samples. Will follow standard procedures in accordance with cGMP, GLP, DEA and company policies and proc ... More
  • 4701 International Blvd, Wilson, NC 27893, USA ● Req #138
    Tuesday, May 17, 2022
    Job Summary Perform a variety of chemical analyses and GMP review of raw materials, packaging components, ancillary solutions, in-process samples, finished product samples, and stability samples in accordance with cGMP, GLP, DEA, and company policies and procedures.  Author and review protocols for method development, method validation, method transfer, and/or process validation.  Execute protocol testing, data review, report writing, and report reviewing.  Conduct equipment validations ... More
  • Stamford, CT, USA ● Virtual ● Req #135
    Friday, May 6, 2022
    Job Summary The Medicaid Program Specialist will be responsible for coordinating the day-to-day operations of Purdue’s Medicaid drug rebate payment program obligations governed by Purdue’s master service agreement with the Center for Medicare and Medicaid Services (CMS) Medicaid Drug Rebate Program and governing regulations. Primary Responsibilities Collaborate with Purdue’s third-party Medicaid processing vendor to validate all state Medicaid rebate invoices in accordance with industry best p ... More
  • Wilson, NC, USA ● Req #116
    Thursday, March 31, 2022
    Job Summary Provides facility leadership for site production operations which includes manufacturing and packaging. The position is responsible for ensuring all operations are carried out in compliance with all applicable regulations of the FDA, OSHA, DEA and company policies and procedures to ensure product quality, employee safety and product security. In addition, will be responsible for providing technical support in determining best method for providing optimum performan ... More
  • Job Summary Provide leadership to the off-shift (2nd and/or hybrid) Operations teams (Manufacturing and Packaging) and support functions ensuring that all operations are completed in compliance with all applicable cGMPs and in a manner to ensure employee safety, product quality and controlled substance security This position is capable of executing assignments independent of direct supervision and providing direct support in the achievement of facility goals and objectives.  This individ ... More
  • Stamford, CT, USA ● Req #95
    Tuesday, October 5, 2021
    Job Summary: The Manager, Pharmacovigilance (PV) Vendor Oversight will partner with the Purdue DSP team, and vendor to provide US PV expertise. The Manager, PV Vendor Oversight and Compliance will also be responsible for assisting PV leadership to provide oversight for DSP vendor activities in accordance with sponsor oversight regulatory requirements. PV Standards, Training & Compliance is a business area expert supporting the Executive Director, Safety Operations, Standards and Compliance ... More