Quality Systems Specialist — Validation & Compliance
Planet Pharma
A leading pharmaceutical company seeks a Quality System Specialist to support global Quality Systems and ensure compliance with applicable SOPs. Responsibilities include managing Quality System applications, gathering user requirements, and supporting system validation activities. The ideal candidate holds a Bachelor’s degree in a relevant field and has 3-6 years of experience in commercial/clinical pharma environments. Proficiency in MS Word and Excel is essential, with knowledge of Veeva Vault and similar tools desirable. This full-time role is based in Waltham, MA. #J-18808-Ljbffr Planet Pharma
- Vertex Pharmaceuticals LLC is seeking a Quality Systems Senior Specialist to support design and delivery of metrics across GxP operations and to provide... ...and trend evaluation. The role involves reviewing validation documentation, batch data, deviations, change controls,...Suggested
$40 - $50 per hour
Quality System Specialist Pay is commiserated with experience and ranges between $40-50/hr. Key Areas... ...and their operations in ensuring compliance and fit for intended use in accordance... ...completion. Ensure system is maintained in a validated state by participating in periodic...SuggestedFull time- Werfen North America is seeking a QA Specialist I to assist in planning, coordinating, and improving the Quality Management System to ensure GMP and FDA/ISO compliance. You will support CAPA, audits, and management reviews under supervision. The role focuses on maintaining...Suggested
$35 - $39 per hour
...Quality Assurance SpecialistPosition DetailsJob Title: Quality Assurance SpecialistEmployment Type: ContractSchedule: Monday... ...documentation and records within the Quality Management System (QMS).Support compliance with applicable quality standards and regulatory...SuggestedContract workTemporary workWork at officeMonday to Friday- ...The Clinical Quality Specialist, under the direction of the CQA management team, will be responsible... ...and their operations in ensuring compliance of clinical studies, vendor management... ...Proficient in MS Word, Excel, and Quality System processes. Experience with Veeva,...Suggested
- ...Description Job Description: The Quality Engineering and Validation Consultant is recognized as an... ...application of quality assurance and compliance. This position coordinates GMP activities... ...communicating gaps for GMP process/systems Provide Quality oversight and review...Work experience placementMonday to Friday
$55 - $65 per hour
...The GMP QA Analytical Sr. Quality Specialist recognized as a subject matter... ...of quality assurance and compliance in support of QA Analytical... ...Supports analytical method validation, verification, and transfer... ...electronic document management systems (e.g., QDoccs, Trackwise,...Contract workTemporary work$50 per hour
Now Hiring: Clinical Quality Specialist Location: Waltham, MA Schedule: Hybrid, 3-5 days per week... ...in clinical quality and regulatory compliance? We're seeking a Clinical Quality Specialist... ...clinical research operations, quality systems, audit activities, and inspection...For contractorsWork at officeLocal areaImmediate start3 days per week- Advantage Technical is seeking a Clinical Quality Specialist in Waltham, MA, offering a hybrid schedule with 3-5 days onsite. The role supports clinical research operations, quality systems, audits, and inspection readiness in a fast-paced pharmaceutical environment. Ideal...
$159.8k - $239.8k
...Director of GMP Operational Quality Assurance is an advanced technical... ...of quality and regulatory compliance. The individual adapts to new... ...for oversight of multiple Validation projects associated with Product... ...-for FG Quality Management System of Global Commercial Finished...Full timeContract workWork experience placementSummer work$72k - $91.5k
...Reporting to the Associate Director, Quality Control – Stability and Trending,... ...Quality Control, Manufacturing, CMC, Validation, and Quality Systems. This role is based in our Lexington... ...completeness, accuracy, traceability, and compliance with applicable procedures Effective...Contract workWork at office$81.15k - $101.96k
...improve both health and quality of life for patients... ...The Quality Assurance Specialist reports to the senior... ...managing the product quality system, including product... ...Chain Security Act) compliance together with supporting... ...requirements. Validate serialization systems...Flexible hoursShift workAfternoon shift$65 per hour
...Job Description The Sr. Specialist GMP QA Operations works with a... ...and maintenance of relevant quality initiatives in support of their... ...alignment with corporate goals and compliance with all regulatory... ...documents in electronic document system Track data for the purpose...Full timeContract workTemporary work- ...people, and our pigs. POSITION SUMMARY The Senior Quality Systems Specialist will be supporting the QA team to implement and manage... ...quality systems Implement process improvements to enhance compliance and improve method and product quality processes (e.g. process...
$65k - $80k
...and our dedication to innovation and quality. We’re passionate about providing... ...components of the Quality Management System (QMS), while ensuring compliance to GMP requirements, FDA & ISO... ...Accountabilities Essential Functions: The QS Specialist I will be expected to support all...Work at officeWorldwide$110k - $120k
...precision, reliability, and quality matter every time. Because... ...Role As a Senior Quality Systems Specialist at Lexington Medical, you... ...execute eQMS computer system validation and 21 CFR Part 11... ...keep product quality and QMS compliance on track as processes and products...$24 - $33 per hour
...solutions and services in more than 110 countries and regions. Quality Systems Associate Summary: Under the direct supervision of... ...perform quality assurance and Training functions to ensure compliance with internal and external regulations and protocol....Hourly payFull timeWork at officeFlexible hours- ...Quality Control SpecialistThe Department of Transitional... ...of Quality Control Specialist Reviewer in Boston.... ...analyzes a statistically valid sample of cases in all... ...decisions to ensure compliance and avoid potential court... ..., laws, rules, systems and regulations governing...Work at officeLocal area
- ...Aerospace in Laconia, NH is searching for a Quality Administrator to join the team.This... ...position supports quality assurance, technical compliance, supplier quality activities, and... ...auditing, qualification testing, and quality system support while providing backup coverage...Contract workFlexible hours
$82.3k - $220k
...visit Job Description Summary The Quality Analyst at Draper provides support for... ...role in maintaining standards, ensuring compliance and supporting quality teams. The incumbent... ...product and process non-conformance systems: identify, document, analyze and correct...Full timeContract workLocal areaFlexible hours$94.2k - $141.2k
...General Summary The GMP Operational Quality Senior Specialist supports the principles and application of quality assurance and regulatory compliance. The incumbent supports or executes a wide range of straightforward activities, and supports new/existing project initiatives...Summer workRemote workFlexible hours2 days per week$61.5k - $89k
...direction of the Manager of Quality Performance, the Quality Performance Specialist plays a key role in... ...accuracy, completeness, and compliance of medical record abstraction and data validation processes that impact... ...across various provider EMR systems, repositories, and...Full timeWork at officeRemote workFlexible hours$55 - $65 per hour
Job Description The Quality Systems Senior Specialist supports design and delivery of impactful metrics and analyses across GxP operations. The incumbent... ...to provide QA support of packaging/labelling validations (primary & secondary packaging as well as serialization)...Contract workTemporary workWork experience placement- Stark Pharma Solutions Inc. in Massachusetts seeks a Technical Compliance Associate to support GMP manufacturing and Quality activities in a regulated environment, focusing on investigations, deviations, NCRs, CAPAs, change controls, and batch documentation. You will partner...
$156.6k - $234.8k
...summary:Biomarker Operational Quality Associate director provides... ...impact and delivery in assuring compliance, excellence in quality and... ...evaluation of process and quality system health and identification of... ...activities (fit-for-purpose validations and associated processes)...Full timeSummer workRemote workFlexible hours2 days per week$77k - $202k
...Description & SummaryThe OpportunityAs a Quality Transformation Consultant, you will... ...sciences clients in digital quality and compliance initiatives within our Advisory practice... ...Interpreting data from manufacturing and quality systems to shape insights and recommendations-...Full timeH1bShift work- STS Aerospace in Laconia, NH is seeking a Quality Administrator to oversee quality assurance, regulatory compliance, supplier quality activities, and special process management... ...) administration, internal audits, and quality system support with backup coverage for key quality...
$66k - $82k
...alternative application process. QA Compliance Specialist Regular Full-Time Bedford, MA, Bedford... ...manufacturing operations meet applicable quality, regulatory, and documentation... ...build hands-on experience in quality systems, manufacturing compliance, and product...Full timeInternshipWork at officeImmediate start- BIOCYTOGEN seeks a detail-oriented Quality Associate to support QA and facility compliance in a non-GLP, research-focused environment. You will collaborate with QA and scientific staff to ensure data integrity and high-quality deliverables for clients. Responsibilities...
$45 - $60 per hour
...Job Description Description Oversee quality operations and at external service providers... ...and documentation in applicable quality systems Compile data for Quality system... ...experience with laboratory testing and method validation Experience Level Intermediate...Contract workTemporary work
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