Manufacturing Specialist - 1st Shift & 2nd Shifts

Job Title: Manufacturing Specialist - 1st Shift & 2nd ShiftsLocation: Fall River, MAJob ID: - 28476Employment Type: Full-Time | 1st & 2nd Shifts (07:00-15:30 / 15:00-23:30)Salary Range: $72,800 - $93,600Work Authorization: U.S. Citizen or Green Card HolderPosition Overview:We are seeking an experienced Manufacturing Specialist (MDI Operations) to support packaging and production activities at a leading pharmaceutical facility. The ideal candidate will possess strong knowledge of cGMP, FDA regulations, and hands-on experience in pharmaceutical packaging operations, preferably in Metered Dose Inhalers (MDI).Key Responsibilities:Coordinate and monitor daily packaging operations to meet production schedules.Ensure compliance with cGMP, FDA, and internal quality standards.Maintain accurate batch records, logs, and deviation documentation.Support investigation of non-conformances and CAPAs.Collaborate with Quality, Supply Chain, Engineering, and R&D teams to resolve operational issues.Create and manage SAP purchase requisitions for materials, equipment, and services.Analyze operational data to identify process improvements and reduce inefficiencies.Support audits and regulatory inspections; ensure compliance documentation readiness.Participate in safety programs and enforce PPE and cleanroom standards.Required Qualifications:Education: Bachelor's degree in Pharmaceutical Sciences, Electrical, Mechanical, Production, or related field.Experience: 5-11 years in packaging, operations, or team management within Pharma, Nutraceuticals, or Medical Devices.Strong understanding of cGMP, FDA regulations, and pharmaceutical packaging processes.Proficiency in SAP, Microsoft Office Suite, and packaging data analysis tools.Excellent problem-solving, organizational, and communication skills.Ability to work independently and collaboratively in a regulated environment.Preferred Qualifications:Experience in Metered Dose Inhaler (MDI) or inhalation product packaging.Familiarity with writing and revising cGMP records and SOPs.Experience in compliance and regulatory audits.Physical Requirements:Stand or walk for extended periods.Lift up to 50 lbs when required.Use of PPE (respirator, goggles, gloves, etc.) required.Benefits:Competitive salary and annual bonus potential401(k) with company matchHealth, dental, and vision insuranceHealth Savings & Flexible Spending Accounts (HSA/FSA)Paid Time Off (vacation, sick, holidays, parental leave)Short-term & long-term disability coverageEmployee discounts and other perks