Archives

Senior Analyst, SAP FICO – Exton, PA 1 Year Contract Role is with a Pharmaceutical Client at their R&D manufacturing facilities located in Exton PA and is kicking off a project in early May 2017 time frame to set up SAP capabilities in order to be able to manufacture commercial product. SAP is already utilized at this …

Contract to Hire Based in RTP – North Carolina Duties: Responsible maintaining an advanced level of knowledge/understanding of the current Good Manufacturing Practices (cGMP) and Parenteral Manufacturing / Operations and Practices. Additionally, person is expected to continue expanding Process/Equipment Qualifications and to execute the manufacturing of parenteral drug products- in accordance with cGMPs, Company Policies/Performance …

Manufacturing Technician Temp to Perm – Maryland Duties: To support the manufacture of Commercial Gliadel wafers, including execution of approved SOPs and batch records to produce a quality product according to GMP guidelines. Takes responsibility for manufacturing a quality product, performs equipment cleaning and maintenance per approved procedures, reviews and edits documentation, and supports protocol …

Manufacturing Technician (2 Open)   1 Year Contract – Baltimore, MD The Manufacturing Technician II (POLYMER) supports the manufacture of Commercial Gliadel wafers, including execution of approved SOPs and batch records to produce a quality product according to GMP guidelines Takes responsibility for manufacturing a quality product, performs equipment cleaning and maintenance per approved procedures, …

Senior Packaging Equipment Engineer 1 Year Contract – Raleigh, NC Duties: This position will support Production Operational Units (OSD, OMO, Parenteral, and Gliadel), and PAR&D by providing the experience, technical expertise, leadership, and project management skills required to evaluate, select, procure, integrate, and validate any equipment needed for the current or future production needs of …

QA Inspector 6-12 Month Contract – Baltimore, MD   Provides routine QA support for the GMP manufacturing activities. Performs a variety of production-related inspections to ensure compliance with policies, practices and/or standard operating procedures. Takes appropriate measures to consistently produce error-free work. Supports QA Systems with administrative support, projects and special assignments. 1. Performs In-Process …