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Complaints and Compliance Supervisor

Nutramax Laboratories

·

Yesterday

Location
Lancaster, SC
Department
Legal
Experience
5+ years
Education
Bachelor
Source
Paylocity

Description

Description

The hours for this position will be Monday - Friday 8:30am - 5pm. 


Summary of the Position 

The Complaints and Compliance Supervisor reports to the Supplier Quality and Compliance Manager. This role is responsible for supervision and oversight of the Complaints program and site Compliance activities for Nutramax Laboratories under the guidelines outlined in the code of federal regulations 21CFR. 


Education and Experience:  B.A. or B.S. in Science or Technical field required.


Minimum Requirements 

  • Must have a  minimum of 5 years of experience in cGMP environment with a minimum of 5  years of customer service experience within an FDA regulated industry.
  • Knowledge of the Regulations 21CFR Part(s) 210, 211, 507 as well as the Dietary  Supplement Regulations 21 CFR 111 is required.
  • Must be proficient Computer Software applications including MS office suite.
  • Must be able to stand, walk, push, and pull in a variety of environments including a Manufacturing and clean rooms. Must have the ability to wear all required Personal Protective Equipment (PPE) based on the auditing environment. Must be able to travel 20 – 30% for domestic audits, (International travel may be needed per quality management).

Roles and Responsibilities

· Supervise Nutramax Customer Complaints and the QA Compliance department. That includes but is not limited to the following responsibilities:

  • Monitor online reseller reviews to identify product or other issues. Report findings to appropriate departments and assist in investigations. 
  • Respond or otherwise address inquiries that are advanced from Customer Service or require additional investigation. 
  • Assist Brand Protection team in counterfeit product investigations  when required.
  • Oversee Nutramax batch record CCRs
  • Supervise the Non-conformance, Complaints, Audit and Supplier Modules in Qualityze.
    • Investigations, assessing, and closing deviations, determining impact of the issues that could affect product safety and quality.
    • Review, track and trend customer complaints/ AERs to ensure customer satisfaction and potential CAPAs are completed for non-conformance.
    • Track and trend Non-Conformances, CAPA’s, Complaints and other quality systems, assesses the risk level associated       with Non-Conformances and escalates the issue to management.
    • Oversee product returns related to complaints.
    • Maintain a strong presence of the QA compliance team in Manufacturing, packaging, and laboratory operations
  • Develop  and implement a performance indicator tracking system and reporting of departmental compliance.
  • Support the Nutramax change control program.
  • Actively support all on site audits (UL, NSF, ISO, FDA, etc.).
  • Communicate effectively with all levels of the organization and departments within the organization and function within a team environment.
  • Train and assist internal departments to understand and comply with Quality and Compliance expectations.
  • Perform other assigned duties and follow verbal and written instructions issued by supervisor or designee related to meeting company goals and objectives.
  • Must be able to effectively communicate with other departments and function within a team environment.
  • Other duties as assigned
  • Regular attendance is required.

Supervisory Responsibilities:  

  • Enforce Safe Work Practices: It's 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's 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

Skills

FDAComplianceCustomer Service

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