- Collect, organize, and migrate data and existing legacy records into validated electronic repositories.
- Issue controlled copies of logbooks to area departments.
- Support the tracking, reconciliation, and archiving of physical and electronic records in compliance with retention procedures and requirements.
- Assist Document Control in formatting, reviews, and approvals.
- Assist in delivering the Quality Docs full user training and user support.
- Support attendance request notifications for weekly Deviation, CAPA, and Change Control meetings.
- Strong knowledge of Microsoft Office, including Word, Excel; Knowledge of SharePoint a plus.
- Strong written and verbal communication skills.
- Ability to work well with a small team in a fast-paced environment.
-
Document Control Clerk
2 days ago
Hayes Instrument Service, Inc. Billerica, United States**Hayes Instrument Service**, a leading electronic test equipment calibration and repair facility, seeks a permanent full time office assistant/document control specialist. Extensive knowledge of Excel and Microsoft office is essential.Primary duties include typing, scanning and ...
-
Document Controller
1 week ago
Keolis North America LLC Somerville, United StatesAt Keolis Commuter Services (KCS), we give every team member—and their ideas—a seat for the journey. We are a diverse team made up of different backgrounds, stories, and perspectives, which is our strength. If you're looking for a career with a company that invests in your future ...
-
Document Control
4 days ago
Randstad Life Sciences US Burlington, United States6 Month Contract · Burlington, MA · PR: $35-41/hour · Shift: · Mon-Fri, 8 hour shift · OR · Wed-Sat 7am-5pm (4, 10 hour shifts) · Job Summary · The Specialist role supporting Document Control and Records Management will be responsible for maintaining documents in compliance with ...
-
Document Control
2 days ago
Randstad Life Sciences US Burlington, United States6 Month Contract · Burlington, MA · PR: $35-41/hour · Shift: · Mon-Fri, 8 hour shift · OR · Wed-Sat 7am-5pm (4, 10 hour shifts) · Job Summary · The Specialist role supporting Document Control and Records Management will be responsible for maintaining documents in complia ...
-
Document Control Specialist
2 weeks ago
Adecco Cambridge, United StatesA Document Quality Control Specialist position (fully remote) is now available through Adecco Medical and Science. In this role, you will be responsible for the quality control review of scientific documents within the Translational DMPK and Clinical Pharmacology group. This posi ...
-
Document Controller
6 days ago
Ascend Elements Westborough, United StatesJob Description · Job DescriptionAscend Elements (AE) is revolutionizing the production of lithium-ion battery materials by establishing a clean and sustainable supply chain using recycled feedstock. Its patented Hydro-to-CathodeTM technology directly synthesizes new cathode mate ...
-
Document Controls Coordinator
6 days ago
Stantec Burlington, United StatesDocument Controls Coordinator OO ) · Description · Stantec Buildings is on a mission to become the world's leading integrated design practice. Our architects, engineers, interior designers, sustainability specialists, and technologists are passionate about the power of design. We ...
-
Document Quality Control Specialist
1 week ago
Adecco Cambridge, United StatesA Document Quality Control Specialist position (fully remote) is now available through Adecco Medical and Science. In this role, you will be responsible for the quality control review of scientific documents within the Translational DMPK and Clinical Pharmacology group. This posi ...
-
Quality Document Control Specialist
3 days ago
Fastnet Software International Inc Cambridge, United StatesJob Description · Job DescriptionShift: 8 am - 5 pm · Veeva GxP Documentation and archival · Processing, Sorting, Organization, and archival of on-site GxP archives and digital archives · Projects related to GxP documentation · Assist with the administration of GxP training · 0-2 ...
-
Quality Document Control Specialist
3 days ago
Integrated Resources, Inc Cambridge, United StatesJob Description · Job DescriptionJob Title: Quality Document Control Specialist · Location: Cambridge, MA · Duration: 6 Months · Job Description: · Duties:Veeva GxP Documentation and archival · Processing, Sorting, Organization and archival of on-site Gxp archives and digital arc ...
-
Cube Hub Inc. Newton, United StatesDescription: · Duration 3 months contract · Location Newton MA · Onsite · Responsibilities: · • Disposition non-conforming material (NCMR). · • Lead and/or participate in product complaint investigations leading to root cause. · • Propose, lead, initiate and follow-up on Corre ...
-
Document Control Specialist
1 week ago
Comrise Newton, United StatesContract- 3 months contract to extension · Payrate: 32.29/hr · Responsibilities: · • Disposition non-conforming material (NCMR). · • Lead and/or participate in product complaint investigations leading to root cause. · • Propose, lead, initiate and follow-up on Corrective Action ...
-
Document Control Specialist
2 weeks ago
Abacus Service Corporation Shrewsbury, United StatesJob Title: Documentation Specialist · Location: 800 Boston Turnpike, Shrewsbury, MA 01545 · Duration: 07 Months Contract · Job Description: · Develops, produces, and maintains a variety of complex technical and user documentation. · Plans and executes writing projects that need ...
-
Document Control Specialist
1 week ago
CONFLUX SYSTEMS Newton, United StatesJob title: Quality Documentation Administrator · Pay rate : $32.29 · Location: MA - Newton - 275, Grove Street (NTN GR) · Description: · Responsibilities: · • Disposition non-conforming material (NCMR). · • Lead and/or participate in product complaint investigations leading to ro ...
-
Document Quality Control Specialist
1 week ago
The Adecco Group Bedford, United StatesA Document Quality Control Specialist position (fully remote) is now available through Adecco Medical and Science. In this role, you will be responsible for the quality control review of scientific documents within the Translational DMPK and Clinical Control Specialist, Quality C ...
-
Document Quality Control Specialist
1 week ago
Adecco USA Bedford, United StatesA Document Quality Control Specialist position (fully remote) is now available through Adecco Medical and Science. In this role, you will be responsible for the quality control review of scientific documents within the Translational DMPK and Clinical Pharmacology group. This posi ...
-
Document Control Specialist I
2 weeks ago
Werfen Bedford, United StatesOverview · Werfen · Werfen, founded in 1966, is a worldwide developer, manufacturer and distributor of specialized diagnostic instruments, related reagents, automation workcells, and data management solutions for use primarily in hospitals and independent clinical laboratories. ...
-
Document Quality Control Specialist
1 week ago
Adecco US, Inc. Bedford, United StatesA Document Quality Control Specialist position (fully remote) is now available through Adecco Medical and Science. In this role, you will be responsible for the quality control review of scientific documents within the Translational DMPK and Clinical Pharmacology group. This posi ...
-
Documentation Control Manager
1 week ago
Onsemi Hudson, United Statesonsemi is seeking a highly effective Documentation Control Manager to be responsible for managing local site documents while also ensuring their accuracy, quality and integrity. The ideal candidate will assure the local site adheres to records retention policies, safeguard inform ...
-
Document Control Specialist
2 weeks ago
24 Seven Talent Westborough, United StatesOur client, a life sciences leader, is looking to bring on a Freelance Documents Records Control Specialist, starting ASAP through EOY. Role will be onsite in Westborough, MA. · Responsibilities/Qualifications: · Develops, produces, and maintains a variety of complex technical an ...
Co-op, Document Control - Waltham, United States - ElevateBio
Description
ElevateBio is a technology-driven cell and gene therapy company, accelerating access to the cutting-edge technologies and expertise to change the future of medicine. Our integrated technologies model offers turnkey scale and biotechnological capabilities to power genetic medicines processes, programs, and companies to their full potential.
The Role:
ElevateBio is looking for a highly motivated and well-organized professional to join the Quality Systems team working in document control and records management. This individual will work closely with the Training, Quality Operations and Digital Quality teams, as well as across cross-functionally with Supply Chain, Manufacturing, Technical Operations and Quality Control teams.
Here's What You'll Do:
ElevateBio is a technology-driven company built to power transformative genetic medicines today and for many decades to come. The Company commercializes its enabling technologies, manufacturing capabilities, and industry-leading expertise through partnerships to accelerate development across a breadth of therapeutic approaches and modalities. The ElevateBio ecosystem combines multiple R&D technology platforms - including Life Edit, a next-generation, full-spectrum gene editing platform; comprehensive cell engineering technologies; and an expanded viral and non-viral therapeutic delivery platform - with BaseCamp, its end-to-end genetic medicine cGMP manufacturing and process development business, to accelerate the discovery and development of advanced therapeutics.
We aim to be the dominant engine inside the world's greatest scientific advancements harnessing human cells and genes to alter disease.
Our Mission:
To power the creation of life-transforming cell and gene therapies, at a speed the world deserves.
Our Vision:
We seek to be the world's most indispensable cell and gene therapy technology company, redefining how companies operate, how products are created and how disease is treated.
ElevateBio is committed to equal employment opportunity and non-discrimination for all employees and qualified applicants without regard to a person's race, color, gender, age, religion, national origin, ancestry, disability, veteran status, genetic information, sexual orientation or any characteristic protected under applicable law. ElevateBio will make reasonable accommodations for qualified individuals with known disabilities, in accordance with applicable law.
