Quality Control Analyst II

Kelly Services; Fort Worth (TX); On-site; USD 55,000 - 61,000; Full time

Job summary

Motion Recruitment Partners in Fort Worth, TX is seeking a Quality Control Analyst II for a 12-month contract. The role involves ensuring lab compliance, developing testing methods, and training staff. You will coordinate with contract labs and maintain QC documentation.

The ideal candidate will have experience with QC in a regulated environment, plus capability to evaluate new technologies and manage deviations and investigations. This is a on-site, temporary assignment.

Responsibilities

• 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.

Skills

Capillary electrophoresis

HPLC/GC

Instrument qualification

Tools

Capillary electrophoresis

HPLC/GC

Instrument qualification

Job description

Job Title: Quality Control Analyst II

Location: Fort Worth, TX 76134

Pay: $42/hr. on W2

Duration: 12 Months with Possible ext.

RESPONSIBILITIES:

• 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.

PREFERRED EXPERIENCE:

• Capillary electrophoresis

• HPLC/GC

• Instrument qualification

Motion Recruitment Partners (MRP) is an Equal Opportunity Employer. All applicants must be currently authorized to work on a full-time basis in the country for which they are applying, and no sponsorship is currently available. Employment is subject to the successful completion of a pre-employment screening. Accommodation will be provided in all parts of the hiring process as required under MRP’s Employment Accommodation policy. Applicants need to make their needs known in advance.