Coordinate and provide shipment quotations to Customer Engagement, Strategic Pricing and Sales departments Collaborate to determine the best shipment method, lead time and prices and all restrictions associated with shipments to best guide the customer when choosing the best shipping method Responsible for coordinating all necessary paperwork and pre approvals with variou

Responsible for the performing of tests and/or calibrations and evaluations or results related to GMP, ISO and non GMP materials and products as appropriate Responsible for troubleshooting basic issues with supervisory oversight Responsible for basic maintenance of equipment Sampling materials to be tested including, but not limited to, weekly water, RM and finished produ

Responsible for the performing of tests and/or calibrations and evaluations or results related to GMP, ISO and non GMP materials and products as appropriate Follow documented procedures and document test data as required Utilize the following techniques to characterize organic and inorganic chemicals FT NMR, GC/MS, GC, HPLC, FT IR and wet chemistry tests Write test proced

Management and disposal of hazardous and non hazardous wastes generated by chemical production laboratories Perform internal pick up and transport of hazardous and non hazardous wastes Coordinate waste pickup by outside vendors Update and maintain accurate waste logs Responsible for wastewater treatment, ensuring city, state, and federal regulations are met, including app

Answer the main telephone line and direct calls to appropriate employees Greet guests upon arrival and direct them to the appropriate employees Distribute orders/tasks via email or SalesForce to the appropriate Customer Engagement team member Responds to customer inquiries regarding shipping, order status, Certificate of Analysis, and Safety Data Sheets Create and email p

Isotope Entry Processing Initiating QC testing or sign thru documentation, coordinating review of data, labeling, and receipt into ERP. Outside Testing coordinating sampling and labeling of materials; initiating PO's; tracking and distribution of results; approving invoices; and communicating with outside laboratories. Coordinate/monitor testing of QC samples for all CIL

Synthesize molecules intended for Clinical Trials Materials (CTM) under cGMP guidelines in CIL's GMP facility Develop and optimize synthetic routes as necessary Create new or revise procedures and batch records as needed Participate in inter departmental meetings Participate in the preparation of project outlines for new projects Maintain the labs with the required equipm

Serve as Administrator of the document control database Assist with document revisions and final distribution after approval Review completed documentation, such as forms, logbooks, and batch records Ensure that appropriate records are properly controlled and manage the storage/filing of controlled documents Participate in the quality management system, which may include

Perform QC submission of GMP products/systems/processing aids Responsible for the inventory management processes and work on improving the inventory accuracy to reduce/eliminate inventory disruption in the supply chain Ensure the right level of safety stock for all critical/noncritical material to limit disruptions to our processes/production schedule Perform inventory co

Create processes and methods to gather supply chain data Analyze data to identify problematic areas and suggest improvements Plan and implement supply chain optimization projects (e.g. warehouse slotting, route planning) Develop requirements and standards (e.g. packaging, procurement, delivery) Oversee inventory procedures Discover the most cost effective shipping modes a

Perform room/line clearances Revision and creation of documents, including SOP's and forms Issuance, review, and tracking of training forms Create/Verify batch records and labels Issue/Review/Reconcile logbooks and controlled forms Assist with the initiation, tracking and final distribution of approved documents Perform any related work as required, based upon experience

Cambridge Isotope Laboratories, Inc. has an outstanding opportunity to work as part of the Good Manufacturing Practices (GMP) team in a fast paced environment based onsite in our Tewksbury, MA location. This is an entry level position for a motivated team player with a background in chemistry or related discipline. The GMP production chemist will be responsible for the ex

Greets guests upon arrival to the reception area and directs them to the appropriate staff member(s) Prints documentation for sales orders. This includes, but is not limited to Pick tickets, Certificate of Analysis (COA), Certificate of Origins (COO), safety data sheets and safety labels Runs tariff code reports for all international orders for shipping department Scans C

Enters into our internal computer system requests for price quotations and sales orders per procedures and customer specific requirements. Orders are received by phone, email and website from customers and/or distributors Make updates or changes to orders as necessary Relying on historical data, process knowledge and judgment, provides additional and/or special handling i

Comply with CIL's general and safety policies. Synthesize complex, non routine and/or routine target compounds generally containing 15N, 18O, D and/or 13C, in some instances using established SOPs. Design and develop new synthetic routes as necessary. Contribute to optimization of chemical routes to the targeted molecules and intermediates, and scalable, cost effective pr