As a QA Inspector your primary responsibility is to perform all In-process and Finished Goods inspections. The QA Inspector facilitates and approves line clearance and reconciles all documents, components, and finished goods labeling with the packaging order, and ensures that all equipment is properly calibrated. Broadly, QA Inspectors are gatekeepers for cGMP compliance. Previous experience in a cGMP packaging or manufacturing industry is preferred. Candidates must demonstrate attention to detail and proficiency in basic math.

Nutra-Med is an Equal Opportunity Employer, including disability and veterans.

As a Forklift Driver your primary responsibilities are to unload, load, and locate pallets, supply components and finished goods to the staging area in the warehouse, and to log the movement of all materials. Forklift Drivers are also responsible for daily inspections of their vehicles to ensure a safe working environment. Experience operating reach, standing, or turret trucks is required. Current forklift certification is preferred, but recertification can be provided upon hiring.

Nutra-Med is an Equal Opportunity Employer, including disability and veterans.

As an Inventory Associate you will assist in maintaining perpetual inventory in the company’s ERP system, Oracle NetSuite. Inventory Associates record all inventory movements and transactions in the warehouse and in the production areas. Inventory Associates also assist in preparing monthly inventory reports for customers. A high school diploma is required, along with proficiency in basic math. Experience in inventory management and the pharmaceutical industry is preferred. Strong organizational and communication skills are essential.

Nutra-Med is an Equal Opportunity Employer, including disability and veterans.

The Regulatory Compliance and Submissions Coordinator will be responsible for maintaining product submissions and maintaining regulatory compliance for the organization in a 24/5 high speed atmosphere. This position reports to the Senior Manager, Regulatory Compliance. The focus of the Regulatory Compliance and Submissions Coordinator is responsible for the review, maintenance, and monitoring of documentation related to the medical devices’ regulatory compliance, such as technical files, design dossiers, and pharmaceutical labeling submission requirements within the US and ICH regulatory compliance field.

Qualifications:

• Must have B.S. Degree in in a technical field (examples: engineering, biology, chemistry).

• Minimum of 2 years of regulatory affairs submissions experience preferrable in the medical device industry to include ICH regulations.

• Minimum of 2 year of relevant labeling experience in a cGMP/FDA, QA regulated environment preferred.

• Knowledge of CFR for CFR 210, 211, 820 and 4

• Knowledge in pharmaceutical and medical devices regulation registration requirements in the CFR and ICH regulations. Global experience is a plus.

• Knowledge of ISO 13485 MMD93/4 and MDR 2017/745, domestic FDA and ICH regulatory requirements, design control activities for medical devices.

• Experience in Daily-Med submissions, Gateway, CDER

• Proficient in Microsoft Office Tools and EQMS software.

• Highly proficient in spoken and written English.

• Effective interpersonal communication skills, both written and oral.

• Attention to detail.

• Develop and implement safety, health, and environmental programs and procedures.

• Review, evaluate, and analyze work environments and design programs and procedures to control, eliminate, and prevent diseases or injury caused by chemical, physical, and biological agents or ergonomic factors.

• Investigate all safety and occupational health related incidents, implement all corrective actions to prevent recurrence, and maintain safe work environment

Minimum Requirements: Master’s Degree in Pharmacy and Health Sciences plus 06 months of experience as an Executive in Supply Chain Management, Occupational Health and Safety, or related field.

Work location for this position will be 118 Algonquin Parkway, Whippany, NJ 07981

COORDINATOR RESPONSIBILITY:

Assist the Director of Project Management and Team on daily basis to ensure all projects are delivered on time, within scope, and budget.

The candidate should possess the ability to collaborate with cross functional teams, including Project Managers, Production Supervisors, QA Supervisors, Supply Chain, Business Development, and Shipping and Receiving team members. This position reports to the Director of Project Management.

POSITION SUMMARY:

The Project Coordinator will be responsible for ordering job specific supplies (e.g., print mats, nitrogen tanks), assisting with order checklists, dispatching customer samples, verifying pricing on PO’s, sending out open order reports to customers, processing basic master specification change controls, maintaining Project Management mailbox and other tasks as assigned by the Director of Project Management.

JOB Qualifications:

• This job requires one year of experience in a business-related field.

• Proficient in Office applications. Knowledge of ERP systems experience, a plus.

• Should have good interpersonal skills and ability to follow through on multi-task responsibilities.

PHYSICAL REQUIREMENTS:

• Should be able to lift minimum 25 lbs.