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...Description Fremont, CA Contract Duration: 5-24 months Rate: Negotiable Responsibilities:Excellent employment opportunity for a Documentation Specialist I in the Fremont, CA area.This position leads all paper/electronic batch record review that is related to manufacturing of...
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...At a Glance
Legrand has an exciting opportunity for a Process Documentation Specialist to join the Finelite Team in Union City, CA .
Process Documentation Specialist Position Description: Working directly with Finelites Lean Manufacturing and Engineering...
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...Engineering & Technology) Department is seeking a service partner to support revisions to our Facility and Engineering Drawings and Documentation database.These drawings are very critical to the site for design and maintenance activities.The drawings are maintained...
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Job Title : Documentation Specialist IIILocation : Fremont, CAHours/Schedule : Mon-Fri, 8AM-5PMCompensation : $35.00- $40.45Type: ( contract, contract to hire or direct)OverviewJoin the global biopharmaceutical that is driven by science and seek to push the boundaries...
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...:
With 5-8 years of experience, you possess deep professional know-how and experience in regulatory affairs.
Candidates have a mastery of regulatory guidance documents and requirements for FDA 510(k) submissions, Health license applications, and EU MDR technical...
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...Job Title:Engineering Documentation Specialist III
Location: Fremont, CA
Hours/Schedule: Mon-Fri, 8AM-5PM
Compensation: $35.00- $40.45
Type: (contract, contract to hire or direct)
Overview
Join the global biopharmaceutical that is driven by science and...
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...other cross-functional supporting teams, make sure the company's regulatory affairs activities are conducted accurately, ethically based... ...are compliant.
Prepare regulatory filing/submission documents and collaborate with the in-country regulatory team to submit...
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...(Must currently live in the SF Bay Area)
The Senior Regulatory Affairs Specialist is responsible for developing strategies for global approvals... ..., sterilization, marketing, labeling, and clinical documents for regulatory compliance.
Review advertising and promotional...
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...team!
We are seeking a detail-oriented individual with excellent organizational skills to fill our new opening for a Document Control Specialist.
This position is responsible for leading, establishing and maintaining both ERP and PLM systems capable of meeting...
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...What You’ll Do:
Perform the coordination and preparation of regulatory submissions for brachytherapy devices and software devices... ...a member of the project steering group.
Submits required documentation/information to local authorities or Varian internal.
Initiates...
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...batch records, labels, specifications and other
pre-production documents for Clinical/Commercial Drug Product in compliance
with FDA... ...,
Manufacturing, Engineering, Packaging, and Regulatory Affairs to ensure that
Clinical/Commercial Drug Products are...
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...robust benefits to support your life while youre working to help others.
Position Overview
The Warehouse Quality and Document Specialist will act as main point person in developing Quality processes, documents and maintaining specialized system data for Warehouse...
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...closure devices and peripheral stents.
This **Senior Regulatory Affairs Specialist** position is an on-site opportunity working out of our... ...products worldwide. The individual may prepare and submit documentation needed for registration worldwide or may oversee such...
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...email me at ""
*Perform the coordination and preparation of regulatory submissions for brachytherapy devices and software devices... ...a member of the project steering group.
* Submits required documentation/information to local authorities or Siemens/Varian internal....
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...Digital Prospectors Document Control Specialist Redwood City , California Apply Now
Recruiter: Hillary Bergstrom (
Phone: (***) ***-****
Position: Document Control Specialist
Location: Redwood City, CA (Hybrid – 3 days onsite)
Length: 6+ Months
Job Description...
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...Pulmonx is looking for an experienced Sr Regulatory Affairs Specialist to join our dynamic Regulatory Affairs Team in Redwood City, CA!... ...the acceptability of quality, preclinical and clinical documentation for submission filing to comply with applicable regulations...
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...Reports to: Senior Director of Regulatory and Quality
Salary Range: 140-160K
Location... ....
The Principal Regulatory Affairs Specialist hired will report to the Senior... ...Develop, Maintain and update regulatory documents such as technical files for CE marking,...
Title: Regulatory Specialist II
Duration: 12 Months with possible extension
Location: Santa Clara, CA 95054
POSITION DESCRIPTION:... ...products worldwide.
The individual may prepare and submit documentation needed for registration worldwide or may oversee such...
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...with the Director of Accreditation, The Accreditation and Regulatory Compliance Specialist manages all aspects of accreditation, regulatory and... ...complaints as needed
Gathers and submits necessary documents to support maintenance of, and changes to, hospital's CDPH...
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...has the drive to succeed.
Auriga Corporation currently has following vacancies in the San Carlos, California Office:
Document Control Specialist
Essential Duties & Responsibilities:
Print and distribute documents as needed.
Scan and upload documents...
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