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Manufacturing Shift Lead (HYAFF), 1st Shift 6:00am-2:30pm

Job in Bedford, Middlesex County, Massachusetts, 01730, USA
Listing for: ANIKA-GCC
Full Time position
Listed on 2026-08-09
Job specializations:
  • Manufacturing / Production
    Manufacturing & Industrial Operations, Production QC/QA, Production Manager, Pharmaceutical Manufacturing
Salary/Wage Range or Industry Benchmark: 44000 - 55000 USD Yearly USD 44000.00 55000.00 YEAR
Job Description & How to Apply Below

What You’ll Do

The Shift Lead oversees day-to-day manufacturing floor operations within a regulated cGMP environment, ensuring safety, quality, and production requirements are met across crosslink and aseptic manufacturing activities. In this role, you serve as the primary on-shift technical resource and lead operator for executing scheduled production activities and maintaining compliance and product quality standards.

How You’ll Contribute
  • Provides direct floor leadership for assigned manufacturing staff during shift operations, ensuring safe, compliant, and efficient execution of production activities.
  • Coordinates and executes daily crosslink manufacturing operations, including organic synthesis, purification, dissolution, formulation, filling, and syringe sterilization within controlled cleanroom environments.
  • Assigns and prioritizes work for shift team members.
  • Resolves real-time production issues to maintain schedule adherence and operational flow.
  • Collaborates with Area Supervisors, Technical Leads, and Engineering to ensure alignment with production schedules and on-time product delivery.
  • Ensures timely and accurate completion of all MRP and ERP transactions.
  • Executes material receipt, consumption, and production reporting activities in ERP systems.
  • Reviews and verifies GMP documentation, including batch records, logbooks, and forms, for accuracy, completeness, and compliance prior to quality submission.
  • Monitors material usage, floor inventory, and production readiness.
  • Communicates schedule changes and supply needs to the team.
  • Ensures compliance with FDA cGMP, ISO standards, OSHA regulations, and EPA requirements across all shift operations.
  • Initiates deviations, investigations, and quality events as needed.
  • Partners with cross-functional teams to determine root cause and corrective actions.
  • Ensures adherence to good documentation practices (GDP).
  • Maintains data integrity across all manufacturing records.
  • Supports training and development of junior staff by identifying skill gaps.
  • Conducts on-the-job training for operators and technicians.
  • Provides performance feedback to supervisors and team members.
  • Acts as a subject matter expert for critical manufacturing processes.
  • Performs hands-on execution of critical process steps when required.
  • Ensures safe work practices across the shift.
  • Escalates safety concerns or risks to management in a timely manner.
  • Performs other duties and projects as assigned.
What It Takes

This role functions as the on-shift operational leader responsible for coordinating manufacturing activities, maintaining compliance, and ensuring production targets are achieved in a highly regulated environment. The Shift Lead must make real-time decisions that impact safety, quality, and delivery performance. The role requires strong technical knowledge, situational awareness, and the ability to guide and support a team in a fast-paced manufacturing setting where errors can result in compliance risks, production delays, or quality issues.

What

You Bring
  • Bachelor’s degree in Engineering, Chemistry, Manufacturing, or related technical discipline preferred, or equivalent relevant experience.
  • Minimum of 6 years of experience in cGMP manufacturing environments.
  • At least 3 years of experience using Material Requirements Planning (MRP) systems, including production transactions and material tracking.
  • Minimum of 2 years of experience in a cGMP-regulated pharmaceutical or medical device manufacturing Lead or similar role, including training or mentoring operators.
  • Strong understanding of FDA, ISO, OSHA, and other applicable regulatory and quality system requirements.
  • Strong verbal and written communication skills with the ability to effectively coordinate team activities on shift.
  • Ability to work flexible hours to support production requirements.
Nice to Have
  • Experience supporting internal audits, inspections, or quality system assessments.
  • Experience working in cleanroom environments and/or using aseptic technique.
  • Experience using SAP or similar ERP systems for manufacturing transactions and reporting.
  • Proficiency in Microsoft Office (Excel, Word, Outlook, PowerPoint).
  • Strong organizational skills with the ability…
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