- Sun Pharmaceuticals, Inc (Princeton, NJ)
- …and compliance documents such as analytical methods, specifications, Method Validation /Transfer Protocols and Reports, SOPs accordingly to companys standards and ... Responsibility:** + Writes technical documents such as methods, specifications, method validation protocols and reports, method transfer protocols and reports based… more
- Sun Pharmaceuticals, Inc (Princeton, NJ)
- …on dermatology, ophthalmology and onco-dermatology. **Job Summary:** The Quality Assurance Specialist is responsible for the batch certification review of site QA ... to manufacturing and packaging records, as well as all supporting documentation . This includes ensuring compliance with Standard Operating Procedures (SOPs),… more
- ATS Automation (Warminster, PA)
- …Industries Requisition ID: 15756 Location: Warminster, PA, US, 18974 Date: Nov 1, 2025 Validation and Documentation Specialist SP Industries Inc.is seeking a ... documentation or equivalent years of relevant experience. (Technical writing/ validation experience for pharmaceutical or biotechnology products preferred.) + One… more
- Insight Global (Hopewell Township, NJ)
- Job Description Our top Pharmaceutical client is seeking a Documentation and Validation specialist to join their External Call Center team within their ... a resource with IVR and Contact Center knowledge to spearhead documentation and validation of processes. The ideal resource will have experience with Salesforce… more
- System One (Princeton, NJ)
- Lead Validation Specialist Location: Remote (Preference for East Coast candidates) Salary: $125,000-$150,000/year + bonus potential About the Role We're seeking ... an experienced Lead Validation Specialist with a strong background in...21 CFR Part 11. + Develop, execute, and maintain validation strategies and documentation for clinical systems.… more
- Cayuse Holdings (Trenton, NJ)
- **Overview** **Job** **Title:** Disaster Recovery Specialist **Location:** Remote **Type:** Independent Contract - Corp to Corp/1099 **Start** **Date:** ASAP **Pay ... **Contract Length:** Long Term Renewable Contract The **Disaster Recovery (DR) Specialist ** plays a critical role in ensuring the organization's technology… more
- Redeemer Health Home Care & Hospice (Meadowbrook, PA)
- …journey. We invite you to apply today. SUMMARY OF JOB The Clinical Documentation Specialist (CDS) performs concurrent review of the medical record to ... Nurse (APN) or completion of medical school. + Must be Certified Clinical Documentation Specialist (CCDS) or Certified Documentation Improvement Professional… more
- TD Bank (Mount Laurel, NJ)
- …Model Risk Management and other stakeholders on activities such as model documentation , risk tiering, validation support, and change classification. The position ... Description:** As a member of the Bank's second line of defense, the ** Specialist , Fraud & Insider Risk Detection Strategy & Modeling Oversight** contributes to the… more
- Redeemer Health Home Care & Hospice (Huntingdon Valley, PA)
- …audit process for risk adjustment models. Ability to identify and communicate documentation deficiencies to providers to improve documentation for accurate risk ... to correctly code diagnoses. The Certified Risk Adjustment Coding/Audit Specialist analyzes and translates concurrent, prospective and retrospective medical and… more
- Sumitomo Pharma (Trenton, NJ)
- …or follow us on LinkedIn. The Trial Master File (TMF) Specialist will be responsible for ensuring that SMPA studies have comprehensive ... inspections. Partnering with the Associate Director, Clinical Business Operations, the specialist ensures accountable functions follow the requirements of the TMF… more
- Actalent (Princeton, NJ)
- …GMP documentation such as batch records, SOPs, test methods, validation protocols, and technical reports for accuracy and compliance. + Execute product-related ... Job Title: Quality Specialist Job Description We are seeking a dedicated Quality Specialist to join our dynamic team within a rapidly growing Cell and Gene… more
- Penn Medicine (Philadelphia, PA)
- …living your life's work? Pathology Full Time (Day Shift) + The Genomic Development Specialist performs a vital role in developing new clinical assays in the Division ... of Precision and Computational Diagnostics (PCD). The Development Specialist will work closely with a team of laboratory professionals to design and perform… more
- Merck (West Point, PA)
- **Job Description** **Purpose of Role:** The Site Analytical Sciences Specialist role is responsible for supporting Analytical Procedure Life Cycle through ... Within Role:** **Technical expertise to support:** + New method introduction ( Validation /Tech Transfer). + New technology introduction. + Assessment and… more
- Actalent (Bala Cynwyd, PA)
- …+ Digest and triage incoming documents for proper routing. + Support CMC documentation and validation processes. Essential Skills + Experience with Veeva Vault ... company in Philadelphia is seeking a junior-level Document Control Specialist to support their Drug Substance team. This role...documents through the system. + Handle large batches of documentation (50-60 docs at a time). + Ensure workflows… more
- Actalent (Bala Cynwyd, PA)
- …+ Digest and triage incoming documents for proper routing. + Support CMC documentation and validation processes. Essential Skills + Experience with GMP, document ... Document Control SpecialistJob Description We are seeking a junior-level Document Control Specialist to support the Drug Substance team. This role is ideal for… more
- Integra LifeSciences (Plainsboro, NJ)
- …patient outcomes and set new standards of care. The **Quality Compliance Specialist ** will provide quality compliance support to the Collagen Manufacturing Center ... in the development, review and/or approval of various Quality System Documentation to ensure that the development, manufacture and distribution of medical… more
- L3Harris (Camden, NJ)
- …other disciplines. + Generate Test Plans for systems and subsystems to ensure validation of requirements + Creation of Documentation in accordance with internal ... Processes. + Experience developing and maintaining Systems Engineering design, validation and qualification processes. + Experience working in a multi-disciplined… more
- Merck (West Point, PA)
- …the thriving West Point site is seeking a Process Automation Engineer (Associate Specialist , Manufacturing Automation) to join the team. Our ability to excel depends ... + Implement, maintain and ensure compliance with SOPs and technical documentation eg Change Management, System Problem Management, System Performance Monitoring. +… more
- Insight Global (Princeton, NJ)
- Job Description Insight Global is looking for a quality admin and documentation specialist for one of our largest consumer packaged goods clients to sit in ... across quality including QMS, doc control, change control, and validation . Other tasks include oversight of translation of global...and guidance on system use, MS support, and global documentation migration support. We are a company committed to… more
- Deloitte (Philadelphia, PA)
- Adobe Experience Platform Data Architect ( Specialist Senior) Our Deloitte Customer team empowers organizations to build deeper relationships with customers through ... and data pipelines. + Data Governance & Quality: Ensure data quality, schema validation , and compliance with privacy regulations (eg GDPR, CCP) through robust data… more
