Senior QA Associate / QA Assoicate I,II - Audits Job Type: Regular Full-Time Location: Seattle, WA Job Description: Be a part of a dynamic and enthusiastic team! Dendreon is seeking a Senior QA Associate who will be responsible to provide direct support for the oversight of all aspects of compliance and vendor qualification activities for Dendreon's Supplier and Vendor Management Program. The Dendreon Quality Systems group works to facilitate a positive and collaborative relationship with our suppliers. You
QA Associate (Sr/I/II)-Quality Compliance, Apheresis Auditor Job Type: Regular Full-Time Location: Seattle, WA Job Description: Dendreon is seeking a QA Associate (Senior/I/II) who will be responsible to provide direct support for the oversight of all aspects of compliance and vendor qualification activities for the Dendreon Network of apheresis collection centers. The Dendreon Quality Compliance group works to facilitate a positive and collaborative relationship with our suppliers. If you thrive in a fast
MEDICAL TESTING ASSOCIATE Requisition Number 35911 City Canon City Physical Location STM-ST THOMAS MORE Department Name CLS STM SPECIMEN MGMT Status Full Time Benefits Eligible Yes Hours per Pay Period 80 Shift Variable Required Education High School Diploma or equivalent (GED) Required Experience Experience Preferred Grade OOO Certificate/Licensure Certification Preferred Contact Information Jillyn Fowler JillynFowler@Centura.org
Summary: To monitor TSR/CSR calls ensuring that the quality of service delivery is at the highest level of excellence.Po sition Objective: To provide outstanding customer satis faction through consistent, friendly and professional call handling, following all PRC and external client policies and procedures, escalating calls, when appropriate.Education:? High School diploma or GEDCollege desirable Profes sional Experience/Qualifications:? Ability to use the phone system? Ability to use computer system? Customer
We have an immediate need for a Process Engineer. The qualified candidate will have a Chemistry background with a degree in a Science. As well this person will easily interact with our Lab and our Production Department. We are looking for someone who will champion and document each step of each flavor of a 100 plus flavor portfolio. Scope of Work o Liaison between Production, Quality Control and Flavor Development. o Work through each ingredient and each process step to truly understand what the
Job Description: Our client is an internationally recognized company looking for a part-time resource to play on their online-enabled games system during the day to monitor user behavior and use tools to suspend accounts, if needed, for violations of terms of use. Responsibilities will include: - Receiving text-based complaints in the database - Reviewing complaints to determine if valid and cases violate the client's terms of use-you may be subjected to offensive content - Playing games in the system to
Recognition and basic understanding of general quality assurance concepts and practices Demonstrate knowledge of...Service Quality Assurance SQA Participates in Quality reviews of...
Howroyd Group of Companies|Laguna Niguel, CA, 92677|
Job Description: We have an immediate need for a Process Engineer. The qualified candidate will have a Chemistry background with a degree in a Science. As well this person will easily interact with our Lab and our Production Department. We are looking for someone who will champion and document each step of each flavor of a 100 plus flavor portfolio. Scope of Work o Liaison between Production, Quality Control and Flavor Development. o Work through each ingredient and each process step to truly understand
Siemens IT Solutions and Services|REDMOND, WA, 98073, USA|2-3
Test Associate - Level 3 Req ID: 13400 # of openings: 1 Work Location City: REDMOND Work Location State: Washington Siemens Office: Issaquah, WA Description Selected candidate will be receiving text based complaints in the database every day. Will be responsible for reviewing the text complaints to determine if the complaints are valid and violate our customer's terms of use. Candidate may be subjected to offensive content. Will also be playing games in the system looking for bad behavior, racial slurs, potential
Our client, a large healthcare company, is seeking multiple QA Associates for their location in Fairfield, OH. On a daily basis, associates will be reviewing plan limitations, patient profiles, and previous prior authorizations. They will also be verifying complete document ion on prescriptions, recognizing and resolving prescription edits, and canceling and returning prescriptions to patients. Qualified candidates must excellent data entry and math skills, and very high attention to detail. With
A mail order pharmacy in the Fairfield area is looking for a Quality Control Associate. Will be reviewing plan limitations, patient profiles, and previous authorizations. They will verify complete and appropriate documentation on prescriptions. Candidate must be able to read prescriptions and identify information on a prescription. Qualified candidates could have experience as a medical assistant, medical transcriptionist or pharmacy technician. This is a contract to hire position. The pay is $11/hr
Chemence Medical Products|Alpharetta, GA, 30005|2-5
- Performs Incoming inspections of raw materials as per company s SOPs and dispositions materials as appropriate. - Participates in supplier qualification process by interacting with vendors and the Purchasing department. - Performs In-Process controls by line clearances and inspections to ensure compliance with specifications. - Performs finished product inspections prior to release for sale. Dispositions approved finished product to be released as appropriate. - Reviews and audits production batch
is currently looking for an experienced Quality Assurance Associate with strong background in the following...is currently looking for an experienced...
B Braun Medical Inc|Center Valley, PA, 18034, USA|3-5
Quality Assurance Associate within our NovoCart Division...Facilitates the establishment of new product specifications and process and product improvements with Quality Assurance Manager...Represents Quality Assurance in design review and new product development...
Potters Industries Quality Assurance Associate Kingman AZ Potters Industries which is...We are seeking a Quality Assurance Associate perform and oversee established testing on...Potters Industries...We are seeking a...
Identify manufacturing deviations or non compliances and reporting to manufacturing and or quality assurance management as appropriate... Identify manufacturing deviations or non compliances and reporting to manufacturing and or quality assurance management as appropriate...
ESSENTIAL FUNCTIONS: The Production Testing Associate (PTA) is responsible for obtaining representative samples of raw materials, bulk solution, work-in-process, and finished products, evaluating these samples for conformance to established quality standards and specifications, and documenting the results of these evaluations. SPECIFIC DUTIES, ACTIVITIES, AND RESPONSIBILITIES: - Standardization and use of simple analytical instrumentation (pH meter, osmometer, torque meter, balance) and measurement
Modern Ad Marketing|Deerfield Beach, FL, 33442|2-5
Description Fast growing on line marketing company is looking for a Quality Assurance Associate...The Quality Assurance QA Associate is responsible for all activities involving quality assurance and compliance with applicable regulatory requirements...
Analytical Biochemistry Labs Inc|Sacramento, CA, 94203|2
The Senior Quality Assurance Associate is responsible for ensuring compliance with GLP regulations and assisting in improving quality processes...coordinating and hosting client and regulatory quality assurance audits assist with the development of...
Dendreon Corporation|Research Triangle Park, NC, 27711, USA|5
Carolina office as part of our Quality Assurance Contract Manufacturing team...position which will develop and implement Quality Assurance policies and procedures in support of...
Process/Test Engineering Associate 0900BE Job Description Apply Online Description Entry level during which an employee receives both functional and organizational training under close supervision. Incumbents carry out assignments within well-defined practices, procedures and policies. Works independently on details of assignments, and has limited decision-making authority; most decisions are made or guided by the immediate supervisor. Decisions/actions may have an impact on the department's/division's
marketing company is looking for a Quality Assurance Associate...The Quality Assurance QA Associate is responsible for all activities involving quality assurance and compliance with applicable regulatory requirements...Quality Assurance QA Associate Description of Quality Assurance QA Associate Fast growing on line...
Quality Assurance Associate Req Number sial 00008664 Location s Lenexa Kansas Job Description 1...a minimum of 2 years direct Quality Assurance experience or an equivalent combination of...
hire opportunity for a Senior Clinical Quality Assurance Associate to join our customer in Newtown...hire opportunity for a Senior Clinical...current experience in a Regulatory or Quality Assurance role within the pharmaceutical industry 3...
MD area is currently hiring a Quality Assurance Associate who will be working in the...MD area is currently hiring a...Minimum of 2 years experience in quality assurance in a GCP environment US citizen...preventive actions Conduct training on pertinent quality assurance issues and procedures Candidate must have...
United BioSource Corporation|San Francisco, CA, 94175, USA|1
QA Associate Job Code :PCVALSF Division :UBC - Clinical Technologies Location :San Francisco CA US 94133 Job Type :Full Time Career Level :Entry Level Education :Bachelor's Degree Category :Biotechnology and Pharmaceutical Job Description : Review validation documents for adequacy and adherence to UBC SOPs Collaborate with departments to ensure validation activities are executed compliantly Apply risk-based principles for computer systems compliance issues in alignment with UBC policies and standards
Pharmaceutical Associates, LLC|King of Prussia, PA, 19406, USA|>3
with the management of various other quality assurance initiatives and programs by Assist with...current experience in a Regulatory or Quality Assurance role within the pharmaceutical industry 3...
QA ASSOCIATE A plastics processor serving the Disposable Medical Device industry, has an immediate opening for an expd QA Associate. Prior exp w/in an ISO 13485:2003 certified co. reqd, technical deg. prefd; plastic extrusion knowledge/exp a big plus. Resp. incl CAPA, supplier evaluation, calibrations, document control, internal auditing. Comp bnfts pkg. Respond to The Morning Call, Box 232, P.O. Box 1260, Allentown, PA 18105. WEB ID# MC22256 Source - Morning Call. Job Requirements: Please
Helpmates Staffing Services|Cerritos, CA, 90703, USA|3
Position Document Custody Quality Assurance Associate Location Cerritos Date Posted 10 29...of Cypressis looking for Document Custody Quality Assurance Associates...Position Document Custody...to the development and implementation of quality assurance standards processes and controls Supporting the...
Current opportunity is for a QA Associate to join the team. Candidate will be required to follow the standard operating procedures in place that govern the packaging of product. This is a contract position, however medical/dental/vision will be available after 30 days! Role Reponsibilities: Performing Q.A. Associate functions in Packaging (including line releases, labeling releases, in-process checks, final examinations, retain sample collections) Performing inspections of all packaging areas (including
Our client, a large healthcare company, is seeking multiple QA Associates for their location in Fairfield, OH. On a daily basis, associates will be reviewing plan limitations, patient profiles, and previous prior authorizations. They will also be verifying complete document ion on prescriptions, recognizing and resolving prescription edits, and canceling and returning prescriptions to patients. Qualified candidates must excellent data entry and math skills, and very high attention to detail. With the urgent
QA Associate Location: Irvine, CA Category: Medical & Science Status: Temporary/Contract Reference: US_EN_2_108174_123312 Salary: N/A Posted: April 14,2009 Adecco Medical and Science offers excellent positions for all career levels. Please email your resume/CV to: mo.ouranos@adeccona.com and you may call me at 760-579-0833. Thank you Mo Adecco Medical & Science, a division of the world leader in the recruitment of medical and scientific professionals, has an immediate opening for a QA Associate to work
Responsible for activities involving quality assurance and compliance with applicable regulatory requirements...Functional Description Responsible for activities involving quality assurance and compliance with applicable regulatory requirements...
ClinForce is currently seeking a Quality Assurance QA Associate for New York NY...Implement Quality Assurance plans and audits for ongoing projects and studies...years as a GCP auditor or Quality Assurance professional with auditing background or equivalent...
Position: Test Development Associate, Math K-12 Assessment Location: Development ACT National Office Iowa City, Iowa Minimum Qualifications: Bachelor's degree in mathematics or a related field and at least 2-4 years of related experience teaching math courses or writing/editing math content, or the equivalent combination of education and experience. Strong communication, organization, and interpersonal skills and experience with personal computers. Work Preferences: Master's degree in a related field and experience
Our bilingual QA associate will be responsible for the running of the Quality Control staff for the night shift. They will make recommendations on staffing and Quality Control Procedures and will train those hired for the night shift. ESSENTIAL DUTIES AND RESPONSIBILITIES include the following. Other duties may be assigned. Performs established quality control procedures in the production environment. Verifies production output by performing pre-defined quality control steps ensuring
Aveva Drug Delivery Systems|Miramar, FL, 33025|3-5
Summary: Responsible for the review of clinical, R&D, and Production commercial batch records to ensure compliance with cGMP's, company procedures and regulatory commitments. Perform SAP transactions as part of the product disposition procedure, and create product release summary requirements. Essential Job Functions: This is not intended as a comprehensive list; it is intended to provide a representative summary of the major duties and responsibilities. Incumbent(s) may not be required to perform all
Located in North County San Diego. Contract to hire, possible direct hire. 65-75K 1. Oversee the day to day activities of the QA department. 2. Prepares documents to send to outside centers, regulatory agencies, and for internal use. 3. Changes, distributes all documents, SOP's, etc. and maintains records of documents. 4. Organizes and updates files in compliance with cGMP and GLP. 5. Reviews QC records to ensure accuracy and completeness and releases bulk peptide batches. 6. Schedule meetings, answer phone
- - - - - - - - - - - - - - - - Job Responsibilities: THIS IS A TEMPORARY POSITION. PLEASE INCLUDE A .DOC VERSION OF YOUR RESUME WITH SUBMITTAL - Performing QA functions in Pharmaceutical packaging (including line releases, labeling releases, in-process checks, final examinations, retain sample collections - Performing inspections of all packaging areas including equipment, components prior to start, during and after operation - Performing first and second checks - Perform