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Quality Control Analyst
Job Location:
Job Location:
Holly Springs, MS - USA
Monthly Salary:
Not provided by the employer
Monthly Salary:
Posted:
8 September 2026 (13 hours ago)
Posted:
Application Deadline:
6 December 2026
Application Deadline:
Vacancies:
1 Vacancy
Vacancies:
Job Summary
Job Title: Quality Control Analyst
Duration: 12 months
Shift/Schedule Details: Sunday-Wednesday Standard Business Hours (1st shift)
Location: Holly Springs NC
Job Description:
Primary responsibilities for this position include performing tasks associated with critical testing on raw materials environment utilities validation samples and manufactured materials. The analyst will be responsible for ensuring that QC Microbiology samples are collected tested and reviewed according to quality requirements and results reported are valid accurate and documented per applicable regulatory and corporate requirements. Analyst may be required to perform or participate in tasks associated with method validation and transfers.
Performs testing and associated tasks without errors per applicable SOPs and protocols.
Complies with policies and procedures in order to maintain compliance with legal regulations health and safety and regulatory requirements as written.
Develops and maintains SOPs
Develops expertise in assigned assays/techniques
Authors lab investigation and invalid assay assessments
May be required to perform shift work as required to support the operations
Ideal Background Education Bachelors degree in Scientific discipline and 3 years experience or associates and 5 years of industry experience or equivalent
3 years of laboratory experience OR equivalent preferred.
Intermediate knowledge of GMPs safety regulations and data integrity
Intermediate knowledge of analytical methods and related instrumentation.
LIMS experience preferred
Experience performing Environmental Monitoring within a pharmaceutical environment
Experience performing Bioburden Endotoxin and Sterility.
Minimum Requirements (Must Have):
1 BS/BA in Biology or Microbiology or other related science field
2 Experience with environmental monitoring in manufacturing areas
3 Some experience with working in an analytical testing lab (academic or industry)
Desired Requirements (Nice to Have):
1 Experience working in a cGMP Pharmaceutical Laboratory
2 Experience with Laboratory Information Management Systems (LIMS)
3 Experience performing Bioburden Endotoxin and Sterility
Duration: 12 months
Shift/Schedule Details: Sunday-Wednesday Standard Business Hours (1st shift)
Location: Holly Springs NC
Job Description:
Primary responsibilities for this position include performing tasks associated with critical testing on raw materials environment utilities validation samples and manufactured materials. The analyst will be responsible for ensuring that QC Microbiology samples are collected tested and reviewed according to quality requirements and results reported are valid accurate and documented per applicable regulatory and corporate requirements. Analyst may be required to perform or participate in tasks associated with method validation and transfers.
Performs testing and associated tasks without errors per applicable SOPs and protocols.
Complies with policies and procedures in order to maintain compliance with legal regulations health and safety and regulatory requirements as written.
Develops and maintains SOPs
Develops expertise in assigned assays/techniques
Authors lab investigation and invalid assay assessments
May be required to perform shift work as required to support the operations
Ideal Background Education Bachelors degree in Scientific discipline and 3 years experience or associates and 5 years of industry experience or equivalent
3 years of laboratory experience OR equivalent preferred.
Intermediate knowledge of GMPs safety regulations and data integrity
Intermediate knowledge of analytical methods and related instrumentation.
LIMS experience preferred
Experience performing Environmental Monitoring within a pharmaceutical environment
Experience performing Bioburden Endotoxin and Sterility.
Minimum Requirements (Must Have):
1 BS/BA in Biology or Microbiology or other related science field
2 Experience with environmental monitoring in manufacturing areas
3 Some experience with working in an analytical testing lab (academic or industry)
Desired Requirements (Nice to Have):
1 Experience working in a cGMP Pharmaceutical Laboratory
2 Experience with Laboratory Information Management Systems (LIMS)
3 Experience performing Bioburden Endotoxin and Sterility
Required Experience:
IC
About Company
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