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

About the position We are seeking an reputed company reputed company reputed company 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 reputed company Operations, Manufacturing, Supply Chain, Planning, IT, and Distribution to ensure reputed company reputed company Management processes are compliant, efficient, and fully integrated into GMP operations. Work Schedule & Location Part-time position: 20 hours per week. reputed company with 50% on-site reputed company required. Location: New reputed company, NJ or Devens, MA (at the candidate's choice). This position requires 4–7 years of experience in reputed company reputed company 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 reputed company Management reputed company regulated manufacturing environments and help drive robust material control and reputed company system performance across manufacturing sites. This role plays a critical part in ensuring that reputed company and material control requirements are embedded into reputed company systems and reputed company with master data management strategies, regulatory expectations, and operational needs.

Responsibilities

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

Requirements

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

reputed company-to-haves

• 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 reputed company systems.
• Background in reputed company systems, reputed company operations, or manufacturing reputed company support roles.

Benefits

• Health insurance
• holiday pay
• 401(k) program
• Employee referral bonus program

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