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Product Shipment Supervisor
Job in
North Billerica, Middlesex County, Massachusetts, 01862, USA
Listed on 2026-02-06
Listing for:
UpLIft Nutrition, Inc
Full Time
position Listed on 2026-02-06
Job specializations:
-
Management
Operations Manager, Healthcare Management
Job Description & How to Apply Below
Join to apply for the Product Shipment Supervisor role at UpLift Nutrition, Inc
.
This position is based in Massachusetts and requires presence on-site three days per week.
The base salary range for this position is $95,000 - $135,000 per year, plus a comprehensive compensation package.
We are seeking a highly organized and compliant professional to oversee daily operations of packaging, labeling, and documentation of product shipments, inventory control, and quality assurance.
Duties and Responsibilities- Oversees daily operations and schedules for the team handling product packaging, labeling, and shipment.
- Facilitates clear concise communication between team members, management, and external groups.
- Ensures that operations are performed per established SOPs and that data collection aligns with cGMPs, company standards, and regulatory requirements.
- Develops training materials and oversees team member training.
- Collaborates with manufacturing leadership to advance cross‑training and operational excellence initiatives.
- Develops metrics to manage performance, identify leading indicators for process improvement.
- Ensures a safe working environment and trains staff in safety, including handling hazardous radioactive materials.
- Has strong understanding of ERP systems for managing inventory, supplies, and raw materials for critical processes.
- Executes all phases of performance reviews, including goal setting and reviews.
- Manages performance and provides coaching, mentoring, and development; handles performance issues and corrective actions.
- Participates in continuous review/upgrade of shipment / logistics functions to achieve high performance, efficiency, and flexibility.
- Interacts with external regulatory inspectors (FDA, EMEA, DOT, NRC, etc.) and compliance auditors during in‑plant inspections, ensuring timely corrective actions (CAPA).
- Provides strong quality commitment by maintaining up‑to‑date knowledge of current and emerging U.S. and international guidelines (FDA, DOT, IATA, cGMP).
- Writes and reviews investigational reports, SOPs, and tracks quality events (deviations, investigations, CAPAs).
- Tracks departmental spend and manages internal budgets, exercising good judgment with expenses.
- Bachelor’s degree in science, engineering, biochemistry, or related discipline, or equivalent experience.
- Two years of experience leading operational personnel; five years if no bachelor’s degree.
- Minimum of two years in a regulated manufacturing environment.
- Combination of education, training, and experience may be considered in lieu of above requirements.
- Broad knowledge of cGMPs and applicable regulatory compliance requirements.
- Excellent interpersonal skills with ability to collaborate across all management levels.
- Detail‑oriented, multitasking ability.
- Ability to lead others and adapt to changing priorities.
- Willingness to work scheduled overtime and on evenings, weekends, or holidays as required.
- Detailed understanding of ERP/MRP and inventory control systems.
- Knowledge of timely cycle counts and accurate inventory transactions.
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