QC Chemist I: Analytical Lab - Data Integrity & GDP

Alora Pharmaceuticals, LLC.

Fort Worth (TX)

Hybrid

USD 48,000 - 64,000

Full time

12 days ago
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Benefits offered by this job

PPE provided
Respirator provided if needed
Medical expenses covered for respir.

Job summary

Alora Pharmaceuticals, LLC. in Fort Worth, TX is seeking a QC Chemist I to perform qualitative and quantitative analyses of raw materials, in-process and finished drug products in a GMP environment.

You will follow test methods, apply USP concepts, document data with GDP, and support cGMP and DEA compliance while growing your analytical skills and contributing to data integrity.

This entry-level role emphasizes accuracy, organization, confidentiality, and clear communication.

Qualifications

  • Follows test methods and completes testing with supervision.
  • Learns USP concepts for laboratory testing.
  • Develops oral and written communication skills.
  • Follows GDP for all documentation.
  • Demonstrates basic lab skills and understanding of testing equipment.
  • Learns basic cGMP, DEA regulations, and quality procedures for QC lab work.
  • Compiles results and understands data integrity.

Responsibilities

  • Perform qualitative and quantitative analyses of raw materials and packaging components.
  • Analyze in-process and finished drug products, including stability testing.
  • Document data according to GDP and procedures.
  • Support instrument maintenance and cleanliness.
  • Ensure compliance with cGMP and DEA requirements.
  • Communicate results and any issues to supervision.

Skills

Intermediate Excel
Professional demeanor
Reliability
Organization
Attention to detail
Strong communication
Confidentiality

Education

BA/BS in Chemistry
Associate degree in Chemistry
2–4 years of chemistry experience

Tools

Laboratory instruments

Job description

Alora Pharmaceuticals, LLC. in Fort Worth, TX is seeking a QC Chemist I to perform qualitative and quantitative analyses of raw materials, in-process and finished drug products in a GMP environment.

You will follow test methods, apply USP concepts, document data with GDP, and support cGMP and DEA compliance while growing your analytical skills and contributing to data integrity.

This entry-level role emphasizes accuracy, organization, confidentiality, and clear communication.

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