10/28 | Primary Role: This individual will work in the Supplier Quality sub-group of the Shire Human Genetic Therapies Quality Assurance department. This unit oversees contract manufacturing operations, supply chain operations and supplier quality functions performed on behalf of Shire. This position is responsible for successful, timely completion of goals and objectives that strengthen the Quality organ | Shire Pharmaceut... | | 0-2 | map | | | action |
10/15 | Primary Role: This is a second shift position. The hours are Wednesday to Saturday from 1400 - 0030. Responsibilities include the issuance and review of batch records/labels, review of test results, and Unpurified bulk product disposition of licensed product. Perform on the floor batch record review. Interpret documentation to ensure operations meet requirements of cGMP, internal SOPs and company p | Shire Pharmaceut... | | 0-2 | map | | | action |
10/15 | Primary Role: This individual will work in the Central Quality Assurance sub-group of the Shire Human Genetic Therapies Quality Assurance department. This unit oversees centralized functions which support internal and external GMP operations, such as QC, Supply Chain, Materials Management, Validation, Informational Services, Process Development, etc. This individual will support routine management | Shire Pharmaceut... | | 0-2 | map | | | action |
11/23 | Vertex Pharmaceuticals is seeing a QA Specialist to join our Quality Documentation group. The successful candidate: -Presents a more extensive understanding of Quality Assurance concepts and practices -Demonstrates emerging knowledge of applicable regulations and a moderate understanding of the interpretation and application of regulations and compliance concepts -Exercises a degree of independent | Vertex Pharmaceu... | | 2-5 | map | | | action |
11/16 | QA Specialist / GMP Quality Group The Quality Specialist is responsible for independently performing multiple activities in support of Quality initiatives. Applies technical proficiency and attention to detail in troubleshooting, as well as the ability to interpret and execute test plans, data and documentation review and final disposition with minimal supervision. Adapts to new work requests with | Commonwealth Sci... | | 2-5 | map | | | action |
11/11 | QA Specialist The Quality Specialist is responsible for independently performing multiple activities in support of Quality initiatives. Applies technical proficiency and attention to detail in “troubleshooting”, as well as the ability to interpret and execute test plans ,data and documentation review and final disposition with minimal supervision. Basic understanding of Quality Management Systems a | LAB PROS | | 2-5 | map | | | action |
10/28 | General Job Description This position is responsible for all Quality Systems activities involving compliance with applicable regulations for cGMP requirements. Performs manufacturing batch record and data review for the disposition of Phase l- II clinical products. Assist in the implementation and execution of QA systems to support manufacturing of products for clinical use. Independently prepares | Merrimack Pharma... | | 2-5 | map | | | action |
11/03 | JOB SUMMARY: The QA Specialist, (Document Reviewer) is responsible for the review of cGMP records. JOB RESPONSIBILITIES: 1. Review of cGMP documentation associated with batch records, protocols (method qualification/validation, process validation, cleaning qualification/validation, stability studies, installation operation and performance qualification, etc.) 2. Review of records associated with Q | Hyaluron Inc | | 10-20 | map | | | action |
10/23 | When do the words “banking” and “excitement” go together? When the Bank is Needham Bank! We’ve been around for a long time (1892), but don’t let our age fool you. We’re very young and forward-thinking in the way we treat our customers and our employees. However, we’re also old enough to know when it makes sense to expand, and that’s what we’re doing. As we grow, we are looking for some top-notch, d | Needham Bank | | 10-20 | map | | | action |
11/25 | Description: Responsible for providing quality assurance support to manufacturing, testing operations and other support functions relative to the production of commercial and/or clinical products for which Development Quality Assurance retains responsibility. Works closely with manufacturing operations, validation, engineering, testing groups, etc. to provide Quality oversight and support to the p | Pfizer, Inc. | | | map | | | action |
11/23 | Description: The QA Specialist in the Development Quality Unit is responsible for a diverse and challenging set of activities, all of which are related to setting and maintaining quality standards aligned with US FDA GMP and other applicable international GMP regulations and guidances. Activities for which this position may be required to take a lead role include, but are not limited to: drug subs | Pfizer, Inc. | | | map | | | action |