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  • ● Req #152
    Wednesday, August 10, 2022
    Job Summary:   The Quality Assurance (QA) Specialist, Documentation Systems is a position that encompasses several Quality Systems. The position conducts technical quality compliance related activities in accordance with GxP regulations and internal Standard Operating Procedures. Primary responsibilities include coordinating documentation in support of global submissions, routine document revisions, document issuance, and documentation archives.   Primary Responsibili ... More
  • ● Req #150
    Thursday, July 14, 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 policies a ... More
  • ● 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
  • 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
  • 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
  • ● 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
  • 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