Quality Control Analyst

Planet Pharma; Fort Worth (TX); On-site; Full time

Job summary

A leading company in the biotechnology sector is seeking a Quality Control Analyst in Fort Worth, TX. This role involves ensuring lab safety, developing testing methods, and maintaining quality standards. Ideal candidates will have strong analytical skills and experience in quality control processes. Join a dynamic team focused on innovation and quality assurance in pharmaceutical manufacturing.

Benefits

Medical insurance

Vision insurance

Qualifications

• Experience in laboratory procedures and quality control.
• Ability to train other analysts and maintain lab safety standards.

Responsibilities

• Ensure lab cleanliness and safety standards are maintained.
• Develop and qualify new testing methods.
• Write technical reports and standard operating procedures.

Skills

Quality Control

Analytical Skills

Troubleshooting

Documentation

Job description

This range is provided by Planet Pharma. Your actual pay will be based on your skills and experience — talk with your recruiter to learn more.

Base pay range

$20.00/hr - $21.50/hr

Direct message the job poster from Planet Pharma

• Ensure that lab cleanliness and safety standards are maintained. • Develop and qualify new testing methods. • Train other analysts to perform laboratory procedures and assays. • Perform visual inspections of finished products. • Participate in internal assessments and audits as required. • Identify and troubleshoot equipment problems. • Evaluate new technologies and methods to make recommendations regarding their use. • Serve as a technical liaison between quality control and other departments, vendors, or contractors. • Coordinate testing with contract laboratories and vendors. • Write technical reports or documentation such as deviation reports, testing protocols, and trend analyses. • Write or revise standard quality control operating procedures. • Supply quality control data necessary for regulatory submissions. • Receive and inspect raw materials. • Review data from contract laboratories to ensure accuracy and regulatory compliance. • Prepare or review required method transfer documentation including technical transfer protocols or reports. • Perform validations or transfers of analytical methods in accordance with applicable policies or guidelines. • Participate in out-of-specification and failure investigations and recommend corrective actions. • Monitor testing procedures to ensure that all tests are performed according to established item specifications, standard test methods, or protocols. • Investigate or report questionable test results. • Interpret test results, compare them to established specifications and control limits, and make recommendations on appropriateness of data for release. • Identify quality problems and recommend solutions. • Evaluate analytical methods and procedures to determine how they might be improved. • Complete documentation needed to support testing procedures including data capture forms, equipment logbooks, or inventory forms. • Calibrate, validate, or maintain laboratory equipment. • Compile laboratory test data and perform appropriate analyses. • Conduct routine and non-routine analyses of in-process materials, raw materials, environmental samples, finished goods, or stability samples

Seniority level

• Seniority level

  Associate

Employment type

• Employment type

  Contract

Job function

• Job function

  Science, Quality Assurance, and Administrative

• Industries

  Biotechnology Research, Pharmaceutical Manufacturing, and Medical Equipment Manufacturing

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Inferred from the description for this job

Medical insurance

Vision insurance

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