Mastech Inc.
Quality Assurance Supervisor
Mastech Inc., Lancaster, South Carolina, us, 29721
Mastech Digital is an IT Staffing and Digital Transformation Services company.Mastech Digital
provides digital and mainstream technology staff as well as Digital Transformation Services for all American Corporations. We are currently seeking a
Quality Assurance Supervisor
for our client in the
Manufacturing
domain. We value our professionals, providing comprehensive benefits and the opportunity for growth. This is a
Permanent
position, and the client is looking for someone to start immediately.Duration:
Full-timeLocation:
Lancaster, South CarolinaSalary:
As per Market StandardsRole:
Quality Assurance SupervisorPrimary Skills:
Quality AssuranceRole Description:
As a
Quality Assurance Supervisor , you must have at least 5 years of experience in Quality Assurance within the nutritional supplement and/or pharmaceutical products manufacturing industry.As the Quality Assurance Supervisor, you will report to the Senior Quality Assurance Manager and oversee Quality Assurance Generalists and Label Issuance. This role supports daily operations and activities in these departments to meet product and service Quality Assurance requirements.Roles and Responsibilities:QAG and production process monitoringLabel Cage operations and personnelProtocol reviewCollaboration with Production Supervisors to resolve production issuesReview of Standard Operating Procedures (SOPs)Oversight of environmental condition records and response to deviationsEnsuring compliance with cGMP requirements, regulations, industry standards, and company policiesConducting investigations, assessing and resolving deviations impacting product quality, safety, and purityReviewing Preventive Maintenance (PM), Pest Control, Calibration records, etc.Collaborating with Production, New Product Development, and other departments on Quality Systems activitiesEnsuring product quality and adherence to government regulations, industry standards, and company policiesImplementing processes to ensure compliance with regulations, standards, and company policiesAbility to work varying shift hours as neededEffective communication with other departments and teamworkPerforming other assigned duties as requiredEducation and Experience:
A Bachelor's degree in a Science major or concentration, supplemented by continuing education credits or certifications from a reputable professional society in the pharmaceutical industry.- Minimum of 5 years' experience in Quality Assurance within the nutritional supplement and/or pharmaceutical products manufacturing industry.- The QA Supervisor should have 3-5 years of experience in an FDA-regulated manufacturing environment, with at least 3 years specifically in Quality Assurance or Quality Control. Prior FDA or equivalent inspection experience is highly advantageous.Education:
Bachelor’s degree in computer science, Electrical/Electronic Engineering, Information Technology or another related field or Equivalent.Experience:
Minimum 5 years of experience.Relocation:
This position will not cover relocation expenses.Travel:
No.Local Preferred:
Yes.Note:
Must be able to work on a W2 basis (No C2C).
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provides digital and mainstream technology staff as well as Digital Transformation Services for all American Corporations. We are currently seeking a
Quality Assurance Supervisor
for our client in the
Manufacturing
domain. We value our professionals, providing comprehensive benefits and the opportunity for growth. This is a
Permanent
position, and the client is looking for someone to start immediately.Duration:
Full-timeLocation:
Lancaster, South CarolinaSalary:
As per Market StandardsRole:
Quality Assurance SupervisorPrimary Skills:
Quality AssuranceRole Description:
As a
Quality Assurance Supervisor , you must have at least 5 years of experience in Quality Assurance within the nutritional supplement and/or pharmaceutical products manufacturing industry.As the Quality Assurance Supervisor, you will report to the Senior Quality Assurance Manager and oversee Quality Assurance Generalists and Label Issuance. This role supports daily operations and activities in these departments to meet product and service Quality Assurance requirements.Roles and Responsibilities:QAG and production process monitoringLabel Cage operations and personnelProtocol reviewCollaboration with Production Supervisors to resolve production issuesReview of Standard Operating Procedures (SOPs)Oversight of environmental condition records and response to deviationsEnsuring compliance with cGMP requirements, regulations, industry standards, and company policiesConducting investigations, assessing and resolving deviations impacting product quality, safety, and purityReviewing Preventive Maintenance (PM), Pest Control, Calibration records, etc.Collaborating with Production, New Product Development, and other departments on Quality Systems activitiesEnsuring product quality and adherence to government regulations, industry standards, and company policiesImplementing processes to ensure compliance with regulations, standards, and company policiesAbility to work varying shift hours as neededEffective communication with other departments and teamworkPerforming other assigned duties as requiredEducation and Experience:
A Bachelor's degree in a Science major or concentration, supplemented by continuing education credits or certifications from a reputable professional society in the pharmaceutical industry.- Minimum of 5 years' experience in Quality Assurance within the nutritional supplement and/or pharmaceutical products manufacturing industry.- The QA Supervisor should have 3-5 years of experience in an FDA-regulated manufacturing environment, with at least 3 years specifically in Quality Assurance or Quality Control. Prior FDA or equivalent inspection experience is highly advantageous.Education:
Bachelor’s degree in computer science, Electrical/Electronic Engineering, Information Technology or another related field or Equivalent.Experience:
Minimum 5 years of experience.Relocation:
This position will not cover relocation expenses.Travel:
No.Local Preferred:
Yes.Note:
Must be able to work on a W2 basis (No C2C).
#J-18808-Ljbffr