5 manufacturing associate jobs found

Launch Your Career in Environmental Consulting – Make an Impact from Day One! Are you ready to combine your passion for sustainability with the fast-paced world of mergers and acquisitions? Join ERM ’s award-winning M&A Transaction Advisory team, based in Manhattan, NY; Washington, DC; Boston, MA; Rolling Meadows, IL; Philadelphia, PA; or Hartford, CT (hybrid role; open to other locations), and help global corporations and financial institutions navigate environmental, health, and safety (EHS) risks during critical business transactions. This is your chance to work on high-profile projects, collaborate with industry experts, and build a career that truly matters. Why This Role Matters Every transaction has hidden risks—and opportunities. As a Consulting Associate, Environmental Due Diligence , you’ll play a key role in uncovering environmental and compliance issues that shape multi-million-dollar deals. Your insights will help clients make informed decisions,...

Quality Control Documentation Auditor Department: Quality Control Reports to: Quality Control Manager Location: Liverpool Full-Time: A typical work schedule is standard business hours, 8:30 a.m.– 5:00 p.m., with the flexibility to handle escalations or support during peak times or special projects. Pay Schedule: Weekly Non-Exempt: Compensation starts at $44,000 to $48,800 annually, depending on experience. Shift Differential: 2nd Shift, +$1. hour, 3rd Shift, +$2. Hour (Based on hours worked) Benefits: Begin the first day after the first two full months of employment ****The salary range reflects the anticipated compensation for the role and may vary based on several factors, including experience, education, specific skill sets, tenure, and overall fit. We value each person’s contributions and recognize that roles have unique requirements that influence compensation; however, different roles may require...

  Position Summary    The Manager, Compliance  is responsible for  the management of compliance activities for all FFF Enterprises, Inc. business units, including Drug Wholesale Distribution, Specialty Pharmacy, and inventory management solutions .   Specific responsibilities include support for the implementation of compliance initiatives, training, investigation, auditing, monitoring,  reporting  and continuous improvement .         This role reports to  Senior Director, Compliance  and is a full-time hybrid role requiring 2-3 days onsite at a company facility .         Essential Functions and Duties    Continuously  strive to  maintain  full compliance and  high  service quality  for  internal and external customers,  as well as strong  employee relations ,  through  the following  activities:   Proa ctively monitor , assess,  and  ensure  compliance with  all  applicable  federal...

B. Braun Medical, Inc. Company: B. Braun US Pharmaceutical Manufacturing LLC Job Posting Location: Irvine, California, United States Functional Area: Quality Working Model: Onsite Days of Work: Friday, Thursday, Wednesday, Tuesday, Monday Shift: 5X8 Relocation Available: No Requisition ID: 12096 B. Braun Medical Inc., a leader in infusion therapy and pain management, develops, manufactures, and markets innovative medical products and services to the healthcare industry. Other key product areas include nutrition, pharmacy admixture and compounding, ostomy and wound care, and dialysis. The company is committed to eliminating preventable treatment errors and enhancing patient, clinician and environmental safety. B. Braun Medical is headquartered in Bethlehem, Pa., and is part of the B. Braun Group of Companies in the U.S., which includes B. Braun Interventional Systems, Aesculap® and CAPS®. Globally, the B. Braun Group of Companies employs more than 64,000...

Job Summary: This is an experienced level position requiring advance knowledge of Quality Engineering principles, quality systems, and technical problem-solving. The incumbent is fully competent in conventional and advance quality methodologies spanning broad technical assignments. Technical assignments involve applying and refining quality processes, developing improved inspection and verification techniques, and ensuring compliance with internal and external quality standards. The role requires the ability to interpret complex requirements, evaluate risk, lead quality-driven investigations, and implement effective corrective and preventive actions. Assignments may include planning, coordinating, and executing quality engineering task of significant scope whole collaborating closely with engineering, manufacturing, supply chain, and program teams. Frequent supplier interaction and travel is required to explain quality approaches, present data, and resolve issues....