Documentation Specialist Salary at Dosespot BETA

Job Title: Drafter / Documentation Specialist Client: Medical Device Manufacturing Company Duration: 6 months with possible extension Location: Waltham, MA 02453 Shift: 8 AM to 5 PM (Monday to Friday) (Work from office 5 days a week ) Qualifications Education: •BS in a technical field or equivalent experience required. Experience with controlled data a plus. Experience: •3-5 years documentation change management experience in a manufacturing environment required / desired Skills: •AutoCAD and SolidWorks modelling/drafting •Communication skills and attention to detail Core Client Behaviors: •Think Big - Sets ambitious goals, thinks beyond the immediate, and works outside of own area for insight and inspiration to excel. •Own the Outcome - Takes a high degree of personal accountability, ownership, and embraces a customer-centric approach to prioritization, planning, and work. •Test. Decide. Go - Open-minded, willing to try new things, balances risk with agility in a culture of learning a

Company Overview: MACOM designs and manufactures semiconductor products for DataCenter, Telecommunication and Industrial and Defense applications.Headquartered in Lowell, Massachusetts, MACOM has design centers and salesoffices throughout North America, Europe and Asia. MACOM is certified to theISO9001 international quality standard and ISO14001 environmental managementstandard. MACOM has more than 65 years of application expertise withmultiple design centers, Si, GaAs and InP fabrication, manufacturing, assemblyand test, and operational facilities throughout North America, Europe, andAsia. Click here to view our facilities. In addition, MACOM offers foundryservices that represents a key core competency within our business. MACOM sells and distributes products globally via a saleschannel comprised of a direct field sales force, authorized salesrepresentatives and leading industry distributors. Our sales team is trainedacross all of our products to give our customers insights into our e

Job Title: Content Analyst II Location: Cumberland, RI 02864 Duration: 7 plus months (possible hire or long term) Work Type: Candidate will be expected to be in office 3-5 days a week in Cumberland, RI Position Overview: Reporting to the Training and Quality Supervisor with direct daily guidance provided by the Senior SOP and Communications Specialist, the Content Development and Communication Specialist is responsible for the accuracy and documentation of various procedures. This individual will create new, and improve upon existing standard operating procedures, job aids, customer letters, and supporting program execution information. Also, this individual will be responsible for identifying and continually making process approvements in alignment with evolving organizational priorities and strategy. Additionally, this role is responsible for all customer communications in partnership with the Senior SOP and Communications Specialist. Lastly, this role will support the quality and tr

This position will provide the department with AutoCAD and SolidWorks drafting as well as translate red-lined drawings to finished documents related to the Company branding project. This position requires creativity, resourcefulness, attention to detail, compliance to documentation control and applicable procedures and the ability to work independently. Primary Duties: Work cross functionally to support the creation, review and timely release of controlled change activity. Verify proposed changes, update documentation and initiate ECNs Ensure that all applicable procedures are followed. Work with Production Engineering to generate changes and update documentation based on red lines. Support drafting effort by utilizing AutoCAD and SolidWorks to create and update mechanical and electro-mechanical drawings to support business needs Responsible to provide internal customer service support for documentation requests. Qualifications: BS in a technical field or equivalent experience required

**Senior Document Specialist** Do you want to be part of an inclusive team that works to develop innovative therapies for patients? Every day, we are driven to develop and deliver innovative and effective new medicines to patients and physicians. If you want to be part of this exciting work, you belong at Astellas! Astellas Pharma Inc. is a pharmaceutical company conducting business in more than 70 countries around the world. We are committed to turning innovative science into medical solutions that bring value and hope to patients and their families. Keeping our focus on addressing unmet medical needs and conducting our business with ethics and integrity enables us to improve the health of people throughout the world. For more information on Astellas, please visit our website at www.astellas.com . **Astellas Institute for Regenerative Medicine (AIRM)** is a wholly owned subsidiary of Astellas Pharma Inc and focused on the development and commercialization of stem cell and regenerative

Signature Healthcare is Southeastern Massachusetts premier local provider of quality, personalized medical services. We are comprised of the award-winning not-for-profit Signature Healthcare Brockton Hospital; Signature Medical Group (SMG), a multi-specialty physician group of more than 150 physicians practicing in 18 ambulatory locations. We believe our distinctive Signature Healthcare team approach is the way healthcare should be: medical professionals across many locations communicating and collaborating, taking advantage of technologies and resources to make a difference in the lives and health of our patients. Position Summary: The CDS works collaboratively with Coding, Medicine, Nursing, Case Management, the Quality Department and ancillary staffs to perform concurrent analytical review of the medical record to ensure an accurate representation of the patients severity of illness. The goal of the position is to improv e documentation of all conditions and treatments from point of

Location: Boston, Massachusetts, United States (Hybrid ; 2-3) Job Overview: My client is seeking a Clinical Supply Chain Coordinator to manage documentation flow and provide administrative and project support to the Clinical Supply Chain (CSC) team. This role is key to improving departmental efficiency and maintaining compliance with regulatory guidelines (FDA, cGMP/cGLP/cGCP). It offers excellent opportunities for growth at the intersection of science, development, and business. Key Responsibilities: Manage emails and file documents in systems like eTMF, eQMS, Box, and SharePoint Support meetings with agenda prep, minutes, and presentations Track contracts, invoices, and POs Assist with onboarding, documentation, and knowledge management Identify and escalate issues, drive process improvements, and support cross-functional projects Qualifications: 3+ years of administrative experience (high school diploma required; degree preferred) Proficient in MS Office, Adobe, and document managem

Akkodis is seeking a Documentation Specialist I (Scientific) for a 6-month contract with a client. Title: Documentation Specialist I (logistic) Location: Waltham MA 02451 (Hybrid) Contract: 6 months Contract Pay Rate: $30-/hr to $32/hr. (The rate may be negotiable based on experience, education, geographic location, and other factors.) Assist with the editing of shipping documents .to ensure compliance with regulatory requirements and efficient cycle time for shipments leaving R&D sites. Ability to lift up to 30 pounds Potential exposure to extreme heat/ cold room, however not frequent. Must be able to work quickly with a high degree of accuracy. Must possess sound interpersonal and information gathering skills, being able to relate well to others at all levels throughout the organization and have the ability to work in a team environment, effectively interacting with others. Prepare and/or maintain detailed records of all shipments processed. Update and draft SOPs related to the shipp