- Merck & Co. (Rahway, NJ)
- …to what is described in the Pipeline Advertisement.Expand your skills and experience in audit through a career path in the pharmaceutical industry. Become part of a ... make a positive impact on patients' lives.Under the direction of the Client Audit Director (CAD) and the Auditor-in-Charge (AIC), the Senior Specialist … more
- Merck & Co. (Omaha, NE)
- Job DescriptionReporting to our Company's Global Supply Chain Director, the Specialist will support the development and implementation of global trade compliance ... policies, procedures, and related training. The Specialist will interface with internal customers, external vendors, and service providers as needed. This role is a… more
- Legend Biotech USA, Inc. (Raritan, NJ)
- …Support batch review & material release in SAP for In-house reagents. Support Floor Spot-check, audit trail review.Strive to reduce non-conformances in ... in the treatment of multiple myeloma.Legend Biotech is seeking a QA Shop Floor Specialist III as part of the Quality Operations team based in Raritan, New Jersey.… more
- Merck & Co. (Rahway, NJ)
- …to employees and their families. The Compensation and Benefits Senior Specialist is responsible for administering operations initiatives related to our Company's ... Puerto Rico benefits committee approvals, financial oversight, reporting, plan audit (s) validation, regulatory filings, benefits education/outreach) Primary responsible party… more
- Cipla (Fall River, MA)
- …changes, process transformations in line with the evolving business requirements. SAP Support for Production, Warehouse and Quality Handling Audit Trails, CSV ... Job Title IT Specialist Organization Name InvaGen Pharmaceuticals, Inc Location 927...from phase of IT solutioning to Go Live & support . The role needs to interact with Cipla … more
- Insmed Incorporated (NJ)
- …in. Are you?About the Role:We're looking for a Quality Management System (QMS) Specialist on the Analytical Development team to help us expand what's possible for ... Quality Assurance, Regulatory Affairs, Manufacturing, and Analytical team to support timely documentation updates and approvals.Develop and present quality… more
- Cipla (Fall River, MA)
- Job Title : Pkg. Documentation Specialist II FLSA Classification : Professional, Exempt Work Location : Fall River, MA Work Hours: General Shift: 8:30AM - 5:00PM ... is searching for experienced candidates for the position of Documentation Specialist . The Documentation Specialist is responsible for the creation… more
- Legend Biotech USA, Inc. (Raritan, NJ)
- …in the treatment of multiple myeloma.Legend Biotech is seeking a QA Validation Specialist III as part of the Quality team based in Raritan, NJ.Role OverviewThe ... QA Validation Specialist role is an exempt level position with responsibilities...and processes within a cell therapy manufacturing plant to support both clinical and commercial requirements in a sterile… more
- Insmed Incorporated (NJ)
- …\tEngage on CSV Projects as a key team member. Provide guidance and support to ensure Insmed computerized systems are deployed following lifecycle management and ... through participating in release management, change control, periodic reviews, and audit trail reviews.What You'll Do: Provide strategic leadership and decision… more
- Usaa (Plano, TX)
- …of a degree. 6 years relevant experience in risk, compliance, legal or audit within the financial services or insurance industry or specialized technical fields ... develop innovative ideas and scope engagements. Risk Assessment & Audit Proficiency: Experience in performing risk assessments and audits,...(now or in the future) you will need immigration support (ie, H-1B, TN, STEM OPT Training Plans, etc.).… more
