GXP Jobs

Refine Results
1 - 20 of 136 Jobs

SFDC TEST Lead with GxP (Onsite/Hybrid)

W3Global

•

On-site in King of Prussia, Pennsylvania, USA

Contract

Must Skills: SFDC testing, Validation Testing. ALM, Jira, Gxp Description: Must have 15+ years of experience in SFDC and GxP validation testing on pharmaceutical domain both manual and automation testing on onsite/offshore deliverable model handling with multiple applications. Experience in test effort estimation & resources planning across all the projects. Responsible for demand/capacity planning, resource management, stakeholder management Experience in writing/enhancing of Test Plan, Test S
Posted 6 days ago | Updated 3 hours ago

Business Analyst --W2 Profiles Only--Remote

Aorton Inc

•

Remote

Contract

Role: Senior Business Analyst Location: Remote Job description: Must Have Clinical/Pharma BA with GXP/Regulatory experienceCandidates should have 5-6+ years of experience in financial services, including relevant responsibilities.Experience in Financial domain is highly desirable (Knowledge of Anti-Money Laundering (AML), Sanctions, Transaction Monitoring, Know Your Customer (KYC), financial securities, and trading principles).Analyze complex problems, derive options and solutions and present i
Easy Apply
Posted 1 day ago | Updated 1 day ago

IT Quality Validation / System Validation / Pharmaceutical (hybrid)

Kellton

•

Hybrid in Nutley, New Jersey, USA

Contract

I am working on this long term contract position for one of my major Pharmaceutical clients . They are looking for string IT Quality validation and Pharmaceutical industry experience. IT Quality Validation Consultant Prepare computer validation documents such as Validation Plans, User Requirements, Configuration Specifications, Test Protocols, and Summary Reports. Prepare Change Control documentation. Execute test scripts. Perform risk assessments. Must be familiar with 21 CFR Part 11. Consult
Easy Apply
Posted 5 days ago | Updated 9 hours ago

CSV/Validation Lead

Amaze Systems Inc

•

On-site in King of Prussia, Pennsylvania, USA

Full-time, Contract, Third Party

Job title CVS Lead Location KOP, PA(Hybrid) Contract 12+ months JD- Keywords CSV, Computer System Validation, Product Serialization, DSCSA Roles and Responsibilities 10 years' Experience in Validating SAP/N systems in Manufacturing Experienced in CSV activities in Manufacturing related applications like SAP/Non Systems, Product Serialization systems, MES systems Perform review for GxP systems to ensure compliance with regulatory requirements Working knowledge on end-to-end validation of GxP ap
Easy Apply
Posted 5 hours ago

Senior Director, Medical Safety Science

Milestone Technologies, Inc.

•

Hybrid in San Mateo, California, USA

Contract

Sr Director of Medical Safety (Operations) - NO C2C Location: Foster City, CA.(requires on-site time) MUST BE LOCAL CANDIDATES Contract length:6 months to start - possibility of contract to hire. Compensation: The estimated pay range for this position is USD $120/Hr - USD $135/Hr and is an Exempt role. Exact compensation and offers of employment are dependent on circumstances of each case and will be determined based on job-related knowledge, skills, experience, licenses or certifications, and l
Easy Apply
Posted 1 day ago

LMS Administrator

Dynamic Enterprise Solutions Inc

•

Remote

Third Party, Contract

Critical Top Line Accountabilities: Technical SME for all systems and administration for Learning and Development in BTSAssuring quality compliance and regulatory monitoring for BTSPoint of contact for training administration with the BTS Learning Management SystemsResponsibilities Responsible for performing User Account Maintenance and System Support Activities as per established guidelines.Maintain detailed tracking of learning systems administrative tasks ensuring their timely completion in
Easy Apply
Posted 6 days ago | Updated 6 days ago

Project Manager

Tekniforce

•

Hybrid in Raleigh, North Carolina, USA

Contract

We are looking for a Project Manager. This is a six (6) months contract position in Raleigh, North Carolina with our client. In this role you would act as a primary liaison with technical and business stakeholders, manage project costs, risks, and deliverables in companys SDLC process. Responsibilities as Project Manager: Creation and maintenance of project plans, project initiation documents, weekly status reports, closing docs, and scheduling/leading regular meetings with sponsors, stakeholder
Easy Apply
Posted 5 days ago | Updated 1 day ago

IT Quality Validation Consultant

Hired by Matrix, Inc.

•

Hybrid in Nutley, New Jersey, USA

Contract

Do you want more than just another job? Are you ready to team up with an organization that values your contributions? Then Hired by Matrix is for you!Working with some of the US premier companies, we excel at connecting candidates with positive cultures and dynamic teams. We even go the extra mile with our signature Consultant Appreciation Program (CAP) to help them in their future job searches.Hired by Matrix has provided talent solutions to enhance organizations team capacities for over thre
Easy Apply
Posted 5 days ago | Updated 3 hours ago

Sr. Computer Systems Validation Engineer

ACI Group, Inc.

•

Remote

Contract

Sr. Computer Systems Validation Engineer, Remote Contract Remote NO THIRD PARTY RECRUITERS PLEASE! KEYWORDS: Pharmaceutical, Computer Systems Validation Description Seeking a Sr. Computer Systems Validation Engineer to develop Computer System Validation strategies for testing/validation support for clients located throughout North America. Responsibilities Support in building CSV strategy for a newly developed computer system from scratch.Prepare testing (without any previous versions); write t
Easy Apply
Posted 22 days ago

Technical Writer-Onsite-Pittsburgh, PA

Accuro Group

•

Pennsylvania, USA

Part-time, Contract, Third Party

Hello Hope you are doing great, We have an urgent requirement of Technical Writer if you feel interested, please revert me with your updated resume. Position: Technical Writer Location: Pittsburgh, PA 100% Onsite. Duration: 12+ Months Contract Desired Competencies (Technical/Behavioral Competency) Role name: Technical Writer Role Description: Creating technical documentation (Quality Plans, System Design Specifications, SRS, URS, Data Integrity Plan, etc) to support the agile delivery of both
Easy Apply
Posted 7 days ago | Updated 9 hours ago

IT Project manager (SAP, Salesforce, PMP)

DGN Technologies

•

Hybrid in Sunnyvale, California, USA

Contract

Role: IT PROJECT MANAGER (APPLICATIONS SIDE) Location: Sunnyvale, CA (Hybrid) TOP SKILLS: - Project management (Traditional, Hybrid) - Business applications exp (SAP, salesforce, Integrations) - Medical industry experience - PMP, Agile certifications - Strong Communication - Minimum 10+ years experience (nothing less) Important notes: - Local candidate - Experience on business applications - Strong project management experience (All stages) - Preferred to have PMP certification - Medical device
Easy Apply
Posted 26 days ago | Updated 26 days ago

IT Project Manager - QMS/Pharma

NTT DATA Americas, Inc

•

Remote

Contract

IT Project Manager / QMS/Pharma - 24-00894 100% REMOTE Duration - EOY W2 or C2CWe are currently seeking a IT Project Manager - QMS/Pharma to join our team.Job Description: 12+ years of progressive experience in IT Project Management (Pharma/Lifesciences) Ability to partner with GxP Quality Systems & Data Migration Teams to implement QMS modules o Ability to manage/drive multiple concurrent projects Work across multiple time zones to support USA and Europe o Ability to work successfully with cros
Easy Apply
Posted 8 days ago | Updated 3 hours ago

Pharma SQA Lead Support

Adifice Technologies

•

On-site in Columbus, Ohio, USA

Contract

No Visa Sponsorship Must be Pharmaceutical or Medical Device industries 15+ years of experience is required Job Description :- Software Quality Assurance with Review and Approval Experience for SDLC DeliverablesExperience should have earlier in career in SDLC/Software Validation with writing and execution of SDLC deliverables (e.g. MVP, Risk)Assessment (FMEA), Requirements, IQ, OQ, PQ, Trace Matrix, and System Release).Several years of SQA experience with Review and Approval of SDLC deliverabl
Easy Apply
Posted 11 days ago | Updated 11 days ago

Pharma SQA Lead Support

Adifice Technologies

•

On-site in Chicago, Illinois, USA

Contract

No Visa Sponsorship Must be Pharmaceutical or Medical Device industries 15+ years of experience is required Job Description :- Software Quality Assurance with Review and Approval Experience for SDLC DeliverablesExperience should have earlier in career in SDLC/Software Validation with writing and execution of SDLC deliverables (e.g. MVP, Risk)Assessment (FMEA), Requirements, IQ, OQ, PQ, Trace Matrix, and System Release).Several years of SQA experience with Review and Approval of SDLC deliverable
Easy Apply
Posted 11 days ago | Updated 11 days ago

Pharma SFDC Test Lead

eTeam, Inc.

•

Remote

Contract, Third Party

Must have 15+ years of experience in SFDC and GxP validation testing on pharmaceutical domain both manual and automation testing on onsite/offshore deliverable model handling with multiple applications.Experience in test effort estimation & resources planning across all the projects. Responsible for demand/capacity planning, resource management, stakeholder managementExperience in writing/enhancing of Test Plan, Test Strategy defining of in scope , out scope , testing approach , project milesto
Easy Apply
Posted 11 days ago | Updated 6 days ago

Sr. Google Cloud Platform Quality Assurance Specialist

Zachary Piper Solutions, LLC

•

On-site in Atlanta, Georgia, USA

Full-time

Piper Companies is searching for an experienced Google Cloud Platform QA Professional to join a global biopharmaceutical company producing therapies for neurology and rare disease disorders as Senior Quality Assurance (Google Cloud Platform) Specialist . The Sr. QA Specialist will be responsible for the auditing and oversight of all QA compliance GxP activities within their assigned area. The Sr. QA Specialist opportunity is HYBRID and located in Atlanta, GA. Responsibilities for the Sr. QA S
Posted 7 days ago | Updated 4 hours ago

Validation Engineer

Ubertal

•

On-site in West Point, Pennsylvania, USA

Contract

Title: Validation Engineer Location: West Point, PA 19486 Duration: 6 Months Qualifications: Bachelors preferred but Associates acceptable (with good experience).3+ years in process automation or equivalent in pharmaceutical/biotechnology industry.Familiarity with Computer system validation and regulatory GXP requirements.Knowledgeable of S88 Batch Standard.Strong communication and interpersonal skills.Technical expertise in automation control systems (e.g., Emerson DeltaV, AB PLC, FactoryTalk,
Easy Apply
Posted 8 days ago | Updated 4 days ago

Pharma Lab IT Support Engineer - Cambridge MA (Onsite)

Sailotech

•

On-site in Cambridge, Massachusetts, USA

Full-time, Third Party, Contract

Position: Pharma Lab IT Support Engineer Location: Cambridge MA (Onsite) Duration:12 months Required Skills: BS in Science, Computer/Information Technology, Bioinformatics or Engineering. Six plus years of progressively advancing experience in: Pharmaceutical operations or software development in pharmaceutical environment. Process automation of laboratory systems, information systems Proficient knowledge of computer system development life cycle concepts, change control systems and FDA regul
Easy Apply
Posted 19 days ago | Updated 17 hours ago

MES Project Manager

Sunraj Consultant

•

On-site in Lititz, Pennsylvania, USA

Contract

Title: MES Project Manager Location: Lititz, PA (100% Onsite) Duration: 9+ months contract (Potential to extend) Note: The candidate should be fine to work onsite from day one. Job description: The global client is implementing an MES system at this location and is finalizing the vendor or MES products currently. This resource needs to have previous MES implementation experience to drive the project, report on statuses, and keep the project moving, in an Agile methodology. The SI will be respons
Easy Apply
Posted 12 days ago | Updated 6 days ago

Sr. Quality Assurance (Google Cloud Platform) Specialist

Zachary Piper Solutions, LLC

•

On-site in Atlanta, Georgia, USA

Full-time

Piper Companies is actively seeking a Senior Quality Assurance (Google Cloud Platform) Specialist to join a global biopharmaceutical organization producing therapies for neruology and rare disease disorders. The Sr. QA Specialist will be responsible for the auditing and oversight of all QA compliance GxP activities within an assigned area. The Sr. QA Specialist opportunity is HYRBRID and located in Atlanta, Georgia. Responsibilities for the Sr. QA Specialist includes: Provide oversight and
Posted 12 days ago | Updated 4 hours ago