Pharmvista is a fast-growing nutraceutical gummy bear manufacturing company. Since its inception in 2015, the company has created various unique products for the US market. We are currently seeking a Quality Associate to join our QA team. We welcome all qualified applicants.

EDUCATION

• Bachelor’s degree preferred in science or related field of study.
• Associate degree in a science or related field of study with related experience in lieu of bachelor’s degree.
• High School diploma with related experience in an FDA Pharmaceutical environment in lieu of associate degree.

INDUSTRY EXPERIENCE REQUIRED

• 1-3 year’s of experience in a cGMP pharmaceutical/dietary supplement environment.

KNOWLEDGE, SKILLS, AND ABILITIES

• Knowledge of basic or commonly used rules, procedures, and operations typically involves step-by-step instructions and requires some previous training or experience.
• Excellent communication skills with the ability to obtain, clarify, or give information. Interpret instructions, record data clearly and precisely. This is a highly visible position requiring contact with varied levels of staff.
• Experience in working with cross-functional teams
• Intermediate level computer skills with proficiency in Microsoft Office software applications, knowledge, and experience with SAP or related MRP system.
• Ability to apply independent judgment regarding what needs to be done based on standard choices required. Must be able to recognize the existence of and differences among easily recognizable situations with respect to information or transaction available.
  Hours: 7:30 AM to 4:30 PM, Monday through Friday
  Job Type: Full-time
  Pay: $60,000.00 - $65,000.00 per year

Benefits:

• Dental insurance
• Health insurance
• Paid time off
• Vision insurance

Ability to Commute:

• East Hanover, NJ 07936 (Required)

Work Location: In perso

• Perform all applicable QA functions related to manufacturing, packaging, analytical testing, sampling and any other responsibilities which are reasonably associated with QA functions.
• Monitors, performs, and documents sampling/testing and inspection of finished products/raw material/components/in-process samples and documents the results in compliance with cGMP and company procedures.
• Collects finished product samples after completion of manufacturing process and sends samples for analytical testing.
• Knowledge of 21CFR 111, 117 and other applicable regulations preferred.
• Review of C of A’s for all incoming raw materials and packaging components.
• Perform random quality checks on packaging line and manufacturing line.
• Accurately performs in-process inspections while documenting all activities on appropriate forms.
• Review & Complete batch records and issues batch records and associated forms to production.
• Maintains quarantine/release/reject system for raw materials, labeling materials, and dietary supplement products. Notifies Supervisor of any variants to process, material, or non-conforming incidents.
• Help conduct investigations of process deviations and notify production immediately of any problems with in-process testing results.
• Performs and supports all types of validation activities in the manufacturing facility.
• Support audit activities in the building and work with regulatory authorities during audit and provide information to FDA or equivalent.
• Must maintain safe, clean, and organized work areas.
• Supervise and oversee the weighing activities for manufacturing.
• Update label inventory daily, review and approve all labels.
• Work on the new Quality Software and update all quality documents daily.
• Receive, quarantine, release or reject ingredients.
• Maintain and verify all cleaning logs and other logs.
• Any other function relates to quality, manufacturing and supply chain which needs QA support.