Quality Assurance Supervisor - 3rd shift

Nutramax Manufacturing; Lancaster (SC); On-site; USD 65,000 - 85,000; Full time

Job summary

Nutramax Manufacturing in Lancaster, SC is seeking a Quality Assurance Supervisor for a Sunday-Thursday, 11:15pm-7:15am shift. The role requires a High School Diploma with AA/BS preferred and 4+ years in an FDA-regulated manufacturing environment, including 3+ years in QA/QC.

The candidate will supervise QA Inspectors, Label Issuance, and Team Leads, ensuring cGMP compliance and effective investigations. The QA Supervisor will collaborate with Production, New Product Development, and other

Qualifications

• High School Diploma required; AA/BS preferred.
• 4+ years in FDA-regulated manufacturing; 3+ years in QA or QC.
• Prior FDA inspection experience is highly recommended.

Responsibilities

• Supervise QA Inspectors, Label Issuance, and Team Leads.
• Support day-to-day QA operations, techniques, and activities.
• Monitor QAI and Production processes; review protocols.
• Work with Production Supervisors to resolve problems.
• Review SOPs and environmental records; respond to excursions.
• Ensure cgMP compliance; conduct investigations and close deviations.
• Review Pest Control and Calibration records; coordinate QA activities.
• Maintain product quality and conformance to regs and policies.
• Develop processes to assure regulatory conformance; communicate across departments.
• Write and close NCRs; update processes for improvements.

Skills

FDA regulations

GMP knowledge

Quality assurance

QA/QC experience

Supervision

Education

High School Diploma

AA or BS/BA preferred

Job description

Description

The hours for this role are Sunday - Thursday 11:15pm - 7:15am. This is a 3rd shift position.

Education and Experience

This position requires a High School Diploma and preferably a degree (either AA or BS/BA). The QA Supervisor must have at least 4 years of experience in an FDA regulated manufacturing environment, with 3 years specifically in Quality Assurance or Quality Control. Prior FDA or equivalent inspection experience is highly recommended.

Minimum Requirements

The QA Supervisor must have at least 4-5 years of experience in an FDA regulated manufacturing environment, with a minimum 3 years specifically in Quality Assurance or Quality Control in the nutritional supplement and/or pharmaceutical products manufacturing industry. Prior FDA or equivalent inspection experience is highly recommended.

Summary of the Position

The Quality Assurance Supervisor reports to Quality Assurance (QA) Assistant Manager. This person supervises Quality Assurance Inspectors, Label Issuance, and Team Leads. The QA Supervisor supports all the day-to-day operations, techniques, and activities associated with those departments that are used to fulfill the Quality Assurance requirements of the product and/or service.

Roles and Responsibilities

The QA Supervisor is responsible for supervising those individuals within the QA department that include but are not limited to the following:

• QAI and Production process monitoring
• Responsible for label cage operations and personnel
• Protocol review and approval.
• Work with Production Supervisors to resolve production problems
• Review of SOPs
• Reviewing and monitoring environmental conditions records and responding to excursions
• Assuring that all applicable cGMP requirements and regulations are met through compliance to government regulations, industry standards and company policies
• Conducting investigations, assessing, and closing deviations, determining impact of the issues that could affect product quality, safety and purity.
• Reviewing of Pest Control, Calibration records, etc.
• Working with Production, New Product Development, and other necessary departments to maintain awareness of Quality Systems activities.
• Product quality and conformance to government regulations, industry standards, and company policies.
• Developing and deploying processes to assure conformance to government regulations, industry standards and company policies.
• Must periodically be able to work varying shift hours in support of personnel on those shifts.
• Must be able to effectively communicate with other departments and function within a team environment.
• Writing and closing NCRs, review of processes, batch records and procedures and updating as needed for improvement or consistency.
• Performance of other duties as assigned.

Supervisory Responsibilities

• Quality Assurance staff
• Enforce Safe Work Practices: It is the supervisor's responsibility to enforce safe work practices and procedures; failure to do so is an invitation for accidents to occur. Workers must be encouraged to identify unsafe or unhealthful workplace conditions or hazards.
• Correct Unsafe Conditions: Supervisors' must take immediate steps to correct unsafe or unhealthful workplace conditions or hazards within their authority and ability to do so. When an unsafe or unhealthful workplace condition or hazard cannot be immediately corrected, the supervisor must take temporary precautionary measures. Supervisors must follow-up to ensure that corrective measures are completed in a timely manner to address the hazard.
• Prevent Lingering Unsafe or Unhealthful Workplace Conditions or Hazards: It is the supervisor's responsibility to train and periodically remind employees of what to look for and how to correct or report unsafe conditions or hazards. If a hazard is identified, the supervisor must act to correct.
• Incidents Reporting: Immediately ensure 1st aid is provided by a ERT member and ensure there is no immediate danger to others. Arrange additional medical treatment for the employee if necessary. Provide emergency transportation, if needed. Notify additional rescue/response teams if necessary.
• Immediately notify EHS for employees seeking medical treatment for work related incidents. Ensure employee completes their sections of the safety incident report.
• Complete the incident report and email to Incident Response before the end of your shift. Begin incident investigation Secure the scene. Keep it unchanged to accurately collect the facts. Obtain photos if needed.
• Coordinate with EHS to form a cross functional team to perform 5 WHY - Root Cause investigation - Other investigation tools may be utilized for more complicated investigations. Corrective action(s) will be agreed upon by the cross functional team based on the root cause. Once the investigation is complete and agreed upon by the cross functional team, email the completed investigation to Incident Reporting