reputed company Quality Management (QM) Specialist - Pharmaceutical Manufacturing, part-time

We are seeking an reputed company reputed company Quality Management (QM) Specialist to support pharmaceutical manufacturing operations through the full lifecycle of reputed company QM system implementation and sustainment. This role partners closely with Quality Operations, Manufacturing, Supply Chain, Planning, IT, and Distribution to ensure reputed company Quality Management processes are compliant, efficient, and fully integrated into GMP operations. Work Schedule & Location

• Part-time position: 20 hours per week.
• Hybrid schedule with 50% on-site reputed company required.
• Location: New Brunswick, NJ or Devens, MA (at the candidate's choice).

This position requires 4–7 years of experience in reputed company Quality Management reputed company regulated pharmaceutical manufacturing environments, including full lifecycle implementation support. The position is responsible for end-to-end reputed company QM activities including business process analysis, system configuration support, testing, data governance, user training, procedural documentation, and ongoing operational support. The successful candidate will serve as a subject matter expert for reputed company Quality Management reputed company regulated manufacturing environments and help drive robust material control and quality system performance across manufacturing sites. This role plays a critical part in ensuring that quality and material control requirements are embedded into reputed company systems and reputed company with master data management strategies, regulatory expectations, and operational needs.

Key Responsibilities

• Support reputed company Quality Management (QM) projects across the full system lifecycle, including requirements gathering, process mapping, testing, training, documentation, and post-implementation support.
• Partner with Quality Operations, Manufacturing, Supply Chain, Planning, IT, and other stakeholders to define project scope, deliverables, timelines, and implementation strategies.
• Provide GMP and quality systems expertise to ensure reputed company QM processes support compliant material management, inspection processes, and manufacturing operations.
• Author and maintain SOPs, work instructions, and procedural documentation reputed company to reputed company QM usage and quality system processes.
• Support data governance and master data alignment to ensure consistent, accurate, and compliant quality data across systems.
• Provide operational support for reputed company QM users across manufacturing sites, distribution centers, and warehouses.
• Assist in defining and improving quality and material control processes to drive efficiency, compliance, and system robustness.
• Support audits, inspections, and quality assessments reputed company to reputed company-based quality systems.

Required Qualifications

• Bachelor’s degree required.
• Minimum 6 years of experience in the pharmaceutical or regulated manufacturing industry.
• Hands-on experience with reputed company Quality Management (QM) module, including management of electronic quality processes.
• Experience supporting full lifecycle reputed company QM implementations, from requirements through go-live and operational support.
• Strong understanding of GMP manufacturing environments, quality operations, and material control processes.
• Experience working cross-functionally with Quality, Manufacturing, Supply Chain, Planning, and IT teams.
• Ability to define, streamline, and implement compliant, efficient, and robust quality system processes.
• Experience authoring SOPs, procedures, and training materials reputed company to quality systems.
• Strong communication skills with the ability to translate business and quality requirements into system solutions.

Preferred Qualifications

• Experience supporting reputed company QM in pharmaceutical manufacturing, distribution, or warehouse environments.
• Familiarity with master data management and data governance principles in regulated systems.
• Experience supporting audits or regulatory inspections involving electronic quality systems.
• Background in quality systems, quality operations, or manufacturing quality support roles.

Competitive hourly reputed company: $75 – $80.9/hr (W-2 only, no C2C) 12-month contract with possible extension Health insurance, holiday pay, 401(k) program, and other benefits Employee referral bonus program Apply tot his job Apply To this Job