Manufacturing Operations Supervisor - Amneal Pharmaceuticals - NY, US
(2021-04 - 2025-11)
Planned and optimized manpower assignments to consistently meet aggressive production schedules, supporting on-time batch release and uninterrupted supply. Drove daily manufacturing activities through effective communication, leadership, and performance tracking. Defined and monitored production performance standards to evaluate and set future targets. Recommended and implemented documentation and quality improvements to enhance product compliance and consistency.
- Escalated, investigated, and resolved safety and quality issues; supported corrective and preventive action plans.
Supervised
Cytotoxic and Hormonal operations of API Pharmacy, Mixing, Encapsulation, Compression, Packaging and Coating areas, ensuring batch completion on schedule. Reported production metrics and progress to senior management; collaborated with Quality, Warehouse, and R&D teams to meet project timelines. Led and coached a team of technicians and operators; managed performance eval
- Troubleshot production processes and equipment issues to reduce downtime and improve efficiency by 10%. Ensured full compliance with cGMP, FDA 21 CFR Parts (210, and 211), have working knowledge of Part 111 and 117 as well as OSHA regulations. Conducted internal and external cGMP compliance audits; corrected deviations and implemented sustainable CAPA solutions to maintain audit readiness. Reviewed and approved batch records, master production records, and SOPs to ensure regulatory compliance. I
- Performed risk assessments and process gap analyses to proactively strengthen quality systems. Supervised annual performance evaluations for all direct reports. Utilized multiple systems and application and audit readiness, including JDE, Caliber, Vaisala, Qumas, Elemco, SAP, and Leucine (E-logbook). Delegated and managed daily activities of Assistant Supervisors and Group Leaders to maintain workflow efficiency.
- Demonstrated subject matter expertise in specialty product manufacturing, including cytotoxic and hormonal processes. Ensured compliance with PAPRs usage and all safety requirements. Oversaw handling of quality events, deviations, and assessments, as well as coordination of API inventories, calibrations, and preventive maintenance.
- Increased productivity by 10% annually while reducing safety incidents and improving product quality by 10%. Consistently exceeded production targets by over 10% year-over-year.
- Identified and implemented continuous process improvements across the department. Completed training programs, including LinkedIn Learning certifications. Gained hands-on experience in sample preparation and particle size testing (Malvern 2000 and 3000), providing dedicated support to QC analytical testing.
Manufacturing Supervisor - Sciegen Pharmaceuticals - NY, US
(2019-04 - 2021-04)
Oversaw and coordinated daily shift changeover to ensure smooth handoff and continuity of operations. Enforced and maintained cGMP compliance, coaching team members on best practices and process adherence. Planned and allocated manpower effectively based on operational priorities and production needs. Reviewed documentation and batch records to verify execution accuracy in accordance with GMP standards. Ensured a safe and compliant work environment while fostering a culture of safety awareness.
- Monitored production quality to guarantee consistent delivery of high-standard pharmaceutical products. Collaborated cross-functionally with Quality, Safety, and Maintenance departments to resolve issues and align on production goals. Executed and successfully completed multiple management-assigned projects within deadlines. Supported management in critical production-related assignments, contributing to strategic initiatives.
- Tracked, trended, and analyzed documentation errors to identify root causes and implement corrective measures. Oversaw documentation closure and follow-ups based on shipping priorities to ensure timely product release.
- Achieved and exceeded monthly production targets, delivering millions of dosage units on schedule.
- Reduced documentation delays through focused oversight and individualized employee coaching. Proposed and implemented new safety improvements to enhance operational safety performance
Manufacturing Supervisor - Nature's Bounty - NY, US
(2017-06 - 2019-04)
Ensured strict adherence to cGMP and SOPs; managed issue escalation, resolution, and timely follow-up. Oversaw shift start-up, performance coordination, and interdepartmental communication to maintain workflow efficiency. Coached, guided, and counseled associates to drive professional growth, accountability, and skill development. Maintained departmental discipline, respect, and collaboration across teams and shifts.
- Fostered teamwork and a culture of proactive decision-making, enhancing productivity and morale. Managed NCRs, investigations, and deviations; oversaw attendance management, documentation review, and in-process checks. Conducted safety observations to ensure compliance and 100% completion of safety requirements. Supported recruitment efforts by conducting interviews, coordinating onboarding, and training new associates. Evaluated performance of direct reports and provided constructive feedback f
- Created and implemented One Point Lessons and training materials to standardize best manufacturing practices. Monitored production targets, product quality metrics, and adherence to manufacturing schedules. Completed special assignments and critical tasks within established deadlines. Provided recommendations aligned with industry-leading manufacturing and operational best practices.
- Improved product quality by identifying and addressing root causes of quality issues.
- Reduced production downtime through efficient coordination and team support. Consistently met or exceeded monthly production and quality targets.
Manufacturing Supervisor - Cipla Pharmaceuticals USA - US
(2015-07 - 2017-05)
Oversaw and coordinated multi-shift manufacturing and packaging operations to ensure on-time, cost-effective production and shipment of quality products within established budgets and regulatory requirements. Participated in production scheduling and planning, optimizing equipment and workforce utilization to maximize output with minimal resource use. Monitored and enforced compliance with safety regulations, workers' compensation standards, and Occupational Safety and Health Administration (OSHA) requirements.
- Collaborated with subordinate supervisors to align departmental operations with production forecasts and schedules, ensuring smooth and timely product flow. Conducted systematic evaluations of production equipment, recommending upgrades and improvements to enhance process efficiency and reliability. Prepared and presented incident reports, production summaries, and key performance metrics to management; supervised 3 section leaders and 50 operators. Led qualification and validation of new manufa
- Implemented process improvements identified through deviation investigations and CAPA initiatives, enhancing operational performance and product consistency. Planned and managed daily, weekly, and monthly production activities, including granulation, compression, encapsulation, and coating, in alignment with strict schedules. Ensured all production and cleaning equipment remained validated, calibrated, and in optimal working condition. Reviewed cleaning validation and verification protocols for
- Conducted selection, onboarding, and performance evaluation of subordinates to maintain a skilled, high-performing workforce.
- Developed and maintained SOPs for training new operators, ensuring consistent adherence to operational and regulatory procedures.
- Ensured compliance with current Good Manufacturing Practice (cGMP) standards and FDA (21 CFR Parts 210, 211, and 117) requirements through proper implementation of departmental policies and procedures.
- Collaborated with cross-functional teams to maintain quality systems, SOP consistency, and operational integrity throughout production.
- Worked closely with scheduling personnel to meet forecast requirements, resolve capacity constraints, and maintain operational efficiency.
- Conducted comprehensive audits to identify performance gaps and implemented corrective measures that improved productivity and compliance. Reduced operational costs through effective resource allocation, strategic planning, and process optimization initiatives.
Corporate Staff Accountant (Hospitality)/Property Controller - Friendwell Management LLC - New Jersey, US
(2015-03 - 2015-06)
Managed bank reconciliations, accounts payable, and monthly close activities with accuracy and timeliness. Supported senior management with financial reporting, administrative tasks, and issue resolution. Reviewed journal entries, coordinated internally and externally to ensure smooth accounting operations.
Participated in monthly meetings and accounting software training to enhance process efficiency. Delivered training on hotel accounting procedures and compliance requirements. Assisted in inspections and audits, ensuring adherence to corporate and regulatory standards.
- Conducted successful audit visits on behalf of the corporate finance team.
