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Boehringer Ingelheim · 1 day ago

Scientist I

Ridgefield, CT

Contract

Onsite

New Grad, Entry Level

$33/hr - $33/hr

Boehringer Ingelheim is a leading pharmaceutical company, and they are seeking a Scientist I to support formulation research and development activities. The role involves preparation of dosing formulations for toxicology studies, coordination of logistics for shipments, and ensuring compliance with regulatory requirements.

BiotechnologyHealth CareMedicalPharmaceutical

Comp. & Benefits

H1B Sponsor Likely

Responsibilities

Formulation preparation for in-house studies

Planning and conducting formulation research and development activities for preclinical studies

Preparation of oral and parenteral dosing formulations of test compounds for non-clinical early and later-stage toxicology studies

Compile method templates/ batch formulation records/ancillary documents

Handle pharmaceutical materials, excipients, oral dosage forms and parenterals

Coordinate formulation preparation activities with CRO partners, as needed

Support and manage logistics of test item and vehicle/diluent

Organize and facilitate logistics of requests (internal transfers and out-going shipments)

Plan and prioritize per project timeline needs for domestic and international shipments

Execution of requests (out-going shipments or internal transfers). Organize and transfer physical materials per requests from internal laboratories. Prepare material to be shipped to CROs, assemble packaging supplies, and provide temperature monitor to ensure material experience recommended storage conditions during shipment duration

Documentation/Coordination of request: Coordinate shipments, communicate with International (Imports Compliance) and supporting functions, logistics dock, send tracking number to CRO

Inventory management- Receive and store physical materials (test item and vehicle /diluent) per SOPs. Manage inventory lifecycle as per SOP

Prepare records for archival as per SOPs and GLP requirements

Lab duties- Ensuring EHS compliance, and conduction of regular lab inspection. Organization of supplies in the laboratory and in storage area

Excellent organization and communication skills

Know how to use MS Office (Excel, Word, PowerPoint, MS Teams)

Ability to multitask

Proactive attitude

Knowledge of database use a plus

Familiarity with a quality environment (GLP) a plus

Qualification

Formulation preparationPharmaceutical materials handlingInventory managementGLP complianceMS OfficeMultitaskingProactive attitudeDatabase useQuality environment familiarityCommunication skills

Required