Analyst I, Quality Control Incoming Job

Celgene Corporation is a global integrated biopharmaceutical company primarily engaged in the discovery, development and commercialization of innovative therapies designed to treat cancer and immune-inflammatory related diseases in patients with limited treatment options.

The Analyst I, QC Incoming is responsible for the daily operations of Incoming Quality Control. This position is responsible for sampling and inspection of incoming materials, including raw materials, packaging materials, primary components, single-use-system, and miscellaneous materials. This is a 2nd shift position in which overtime hours may occasionally be required.

* Performs sampling and inspection procedures, as necessary, for all incoming materials (raw materials, packaging materials, primary components, single-use-system, and miscellaneous materials). * Uses instrumentation, computerized systems, and tools (such as calipers) to perform analysis of incoming materials in accordance with governing procedures. * Collates and transfers completed data packets to internal customers. * Accurately follows and understands SOP and cGMP requirements, including documentation requirements. * Orders and maintains inventory for sampling, inspection and cleaning consumables. * Cleans and maintains sampling areas and associated equipment/supplies in accordance with governing procedures. * Cleans and maintains inspection areas and associated equipment/supplies in accordance with governing procedures. * Supports performance of preventative maintenance and/or safety evaluations in the sampling and inspection areas. * Assists in troubleshooting problems, under direct supervision. * Assists in revision of documents and completion of project tasks, as assigned. * Perform other duties as assigned.

**Education/Experience Requirements** * Minimally requires an Associate’s degree in a science with 4 years experience, (preferably in a regulated manufacturing environment with cGMP requirements), or a College degree (preferably in a science) with 2 years experience. * An equivalent combination of education, experience and training may substitute. **Computer/Software Skills** * Requires proficiency in basic MS Word, Outlook, Excel **Compliance Knowledge** * Requires ability to deal appropriately with regulatory agencies * Requires general knowledge of cGMP, OSHA, DEA, USP and EP **General Competencies** * Requires flexibility and ability to multi-task * Requires strong written and verbal communication skills * Requires strong organizational and time management skills * Requires strong critical reasoning and decision making skills * Requires strong teamwork and facilitation skills Written Communication * Requires ability to interpret / write general business documents * Requires ability to interpret / write technical documents * Problem Solving * Requires ability to solve routine problems * Level of Supervision * Requires direct supervision * Impact of decisions * Impacts one department * Impacts multiple departments * Requires uniform/ PPE to work in a manufacturing, warehouse, or laboratory environment * Requires screening (full physical, antineoplastic medical surveillance, etc…) * Requires the ability to wear a respirator * Requires safety alertness due to work around hazardous equipment and conditions * Requires personnel monitoring due to handling of hazardous substances * Requires eye examination to show 20/20 correctable vision * Requires doctor’s note if not able to push, pull, reach, balance and/or lift > 20 lbs * Requires set hours by Supervision