- Wipfli LLP (Bedford, NH)
- …offers a career-defining opportunity. Responsibilities Responsibilities: + Manage audit , review, compilation engagements, and multiple teams. Provide performance ... end + Partner with Senior Managers, Directors, and Partners in risk assessment, audit procedures, and reporting . + Oversee daily operations of the audit… more
- Robert Half Management Resources (Marlborough, MA)
- Description We are seeking an experienced and strategic Internal Audit Manager to join a dynamic public manufacturing company headquartered in Marlborough, ... or related field. Advanced degrees preferred. + Experience: 5-8 years in audit ( manufacturing preferred). Strong knowledge of SOX, GAAP, and risk management. +… more
- Bristol Myers Squibb (Devens, MA)
- …products + Support with SAP transactions and workflows with direct and indirect impact on Manufacturing This is a direct people manager role where the manager ... no better place than here at BMS with our Cell Therapy team. The ** Manager , Cell Therapy Supply Chain** is responsible for management and oversight of critical… more
- GAF (Lowell, MA)
- …for consistent and reliable supply of raw materials crucial for GAF Manufacturing . They will lead efforts related to Supplier Quality, including defining ... Systems to uphold product standards and operational excellence. **Job Summary** The Manager of Supplier Quality will provide leadership to assess and mitigate raw… more
- Tecomet (Wilmington, MA)
- **POSITION SUMMARY:** The Quality Assurance Manager oversees the quality management system (QMS) and ensures compliance with AS9100 and other regulations as ... producers. This is an ITAR regulated site. The Quality Assurance Manager Quality Engineering and Inspection teams, manages audits, coordinates corrective actions,… more
- Bristol Myers Squibb (Devens, MA)
- …work and in their personal lives. Read more: careers.bms.com/working-with-us . ** Manager , QC Instrument Specialist** **, Bristol-Myers Squibb Company, Devens, MA.** ... NuGenesis and other software programs; + Current cGMP (Good Manufacturing Practices) regulatory requirements, computerized analytical systems; + Quality management… more
- DEKA Research & Development (Manchester, NH)
- …regulatory requirements (eg, FDA 21 CFR Part 820, ISO 13485). + Support audit readiness by organizing documentation and working with internal teams. What You Will ... strive to make a difference every day through thoughtful engineering, design, and manufacturing . Here at DEKA, some of the most innovative and life-changing products… more
- Nestle (Sudbury, MA)
- …Site SH&E performance improvement. + Compliance - Ensure sites maintain continuous " audit ready" state of compliance with company SH&E policies and procedures as ... regional, or corporate safety and environmental experience within a manufacturing or production environment. + Professional certifications in SH&E-related fields… more
- Bristol Myers Squibb (Devens, MA)
- …to the right location, at the right time while adhering to good manufacturing practices and standard operating procedures. The ability to recognize deviation from ... with Materials Operations Staff, Quality Control, Quality Assurance and Manufacturing . + Collaborate with cross-functional employees & department managers to… more
- Teleflex (Chelmsford, MA)
- …elements including metric reporting and trending, document control responsibilities, and audit execution and participation. The ideal candidate will have a strong ... findings to management. * Assist in the Quality Systems Manager with CAPA's as needed. * Assist in the...needed. * Assist in the preparation and review of audit reports, ensuring timely follow-up on corrective actions. *… more