Manufacturing Quality Assurance Coordinator

Otsuka Pharmaceutical Co., Ltd; New Albany (MS); On-site; USD 40,000 - 66,000; Full time

Job summary

Pharmavite is hiring a Quality Assurance Coordinator to ensure consistent quality across manufacturing processes by reviewing and evaluating documents and records from manufacturing or packaging operations.

The role involves assembling and reviewing documentation, sampling and inspecting bulk components and finished goods, and conducting in-process audits to support programs and procedures. Strong attention to detail and English proficiency are required.

Qualifications

• GED or High school education required.
• One year of experience in a manufacturing environment.
• Experience in quality is preferred.
• Working knowledge of quality system requirements.
• Experience with QA measuring and testing equipment.
• Ability to speak, read, and write English.
• Effective communication and interpersonal skills.
• Computer skills in data entry and processing.
• Ability to conduct mathematical calculations.
• Attention to detail.

Responsibilities

• Assembles and reviews manufacturing or packaging documents to ensure proper disposition.
• Samples, inspects, and reviews documentation of bulk, components, labels, and finished goods to ensure quality standards are met.
• Conducts in-process audits and testing to support company programs and procedures.
• Reviews and dispositions batch records and minor NCRs, and enters disposition in the system.
• Communicates problems to Quality department leaders and resubmits documentation for corrective action.
• Prepares reject notices for non-conforming product, components, or labels to ensure quarantine process is followed.
• Performs other duties as assigned.

Skills

Quality systems

QA testing equipment

English literacy

Communication skills

Data entry

Mathematical calculations

Attention to detail

Education

GED or high school diploma

Job description

Pharmavite is hiring a Quality Assurance Coordinator to ensure consistent quality across manufacturing processes by reviewing and evaluating documents and records from manufacturing or packaging operations.

The role involves assembling and reviewing documentation, sampling and inspecting bulk components and finished goods, and conducting in-process audits to support programs and procedures. Strong attention to detail and English proficiency are required.