Education & Experience

  • High School Diploma required
  • Associate Degree in Science or Health Care or related field or equivalent work experience (Preferred)
  • Familiar with GMP experience
  • Pharmaceutical experience, required
  • Prior experience with quality functions, aseptic techniques, GDP/GMP requirements, material release, investigation skills
  • Knowledge of cGMP principles as it pertains to 21 CFR 210, 211 and 503B regulated environments.

Apply

Qualifications

  • To perform this job successfully, an individual must be able to perform each essential duty satisfactorily while paying close attention to detail.
  • The requirements listed below are representative of the knowledge, skill, and/or ability required.
  • Reasonable accommodations may be made to enable individuals with disabilities to perform the essential functions.

Education & Experience

  • High School Diploma required
  • Associate Degree in Science or Health Care or related field or equivalent work experience (Preferred)
  • Familiar with GMP experience
  • Pharmaceutical experience, required
  • Prior experience with quality functions, aseptic techniques, GDP/GMP requirements, material release, investigation skills
  • Knowledge of cGMP principles as it pertains to 21 CFR 210, 211 and 503B regulated environments.

Apply

Supervisory Responsibilities

None

Qualifications

  • To perform this job successfully, an individual must be able to perform each essential duty satisfactorily while paying close attention to detail.
  • The requirements listed below are representative of the knowledge, skill, and/or ability required.
  • Reasonable accommodations may be made to enable individuals with disabilities to perform the essential functions.

Education & Experience

  • High School Diploma required
  • Associate Degree in Science or Health Care or related field or equivalent work experience (Preferred)
  • Familiar with GMP experience
  • Pharmaceutical experience, required
  • Prior experience with quality functions, aseptic techniques, GDP/GMP requirements, material release, investigation skills
  • Knowledge of cGMP principles as it pertains to 21 CFR 210, 211 and 503B regulated environments.

Apply

Essential Duties & Responsibilities

  • Review batch records for accuracy, documentation errors, completeness.
  • Review reports and logs for accuracy, documentation errors, completeness.
  • Deviations, Complaints, Out of Specification investigation and reporting. Trending of data for each to ensure overall compliance with regulatory standards.
  • Preventative Maintenance and Calibration program scheduling and management.
  • Assist with continuous staff training on cGMP to enhance the quality culture.
  • Training on other quality policies and procedures as implemented.
  • Assist in generation, review, and revision of standard operating procedures.
  • Assist in the printing and review of product labels.
  • Assist in the filing, scanning, and copying of controlled documents.
  • Ability to interpret federal and state regulatory policies and procedures.
  • Ability to perform technical writing required for SOPs and non-conformance investigation.
  • All other tasks as assigned by the Quality Assurance Management.

Supervisory Responsibilities

None

Qualifications

  • To perform this job successfully, an individual must be able to perform each essential duty satisfactorily while paying close attention to detail.
  • The requirements listed below are representative of the knowledge, skill, and/or ability required.
  • Reasonable accommodations may be made to enable individuals with disabilities to perform the essential functions.

Education & Experience

  • High School Diploma required
  • Associate Degree in Science or Health Care or related field or equivalent work experience (Preferred)
  • Familiar with GMP experience
  • Pharmaceutical experience, required
  • Prior experience with quality functions, aseptic techniques, GDP/GMP requirements, material release, investigation skills
  • Knowledge of cGMP principles as it pertains to 21 CFR 210, 211 and 503B regulated environments.

Apply

About the Job

This role assists the Quality Assurance department to ensure quality products and care to customers by performing the following duties.

Essential Duties & Responsibilities

  • Review batch records for accuracy, documentation errors, completeness.
  • Review reports and logs for accuracy, documentation errors, completeness.
  • Deviations, Complaints, Out of Specification investigation and reporting. Trending of data for each to ensure overall compliance with regulatory standards.
  • Preventative Maintenance and Calibration program scheduling and management.
  • Assist with continuous staff training on cGMP to enhance the quality culture.
  • Training on other quality policies and procedures as implemented.
  • Assist in generation, review, and revision of standard operating procedures.
  • Assist in the printing and review of product labels.
  • Assist in the filing, scanning, and copying of controlled documents.
  • Ability to interpret federal and state regulatory policies and procedures.
  • Ability to perform technical writing required for SOPs and non-conformance investigation.
  • All other tasks as assigned by the Quality Assurance Management.

Supervisory Responsibilities

None

Qualifications

  • To perform this job successfully, an individual must be able to perform each essential duty satisfactorily while paying close attention to detail.
  • The requirements listed below are representative of the knowledge, skill, and/or ability required.
  • Reasonable accommodations may be made to enable individuals with disabilities to perform the essential functions.

Education & Experience

  • High School Diploma required
  • Associate Degree in Science or Health Care or related field or equivalent work experience (Preferred)
  • Familiar with GMP experience
  • Pharmaceutical experience, required
  • Prior experience with quality functions, aseptic techniques, GDP/GMP requirements, material release, investigation skills
  • Knowledge of cGMP principles as it pertains to 21 CFR 210, 211 and 503B regulated environments.

Apply

Benefits
– Health insurance
– Paid time off
– Dental insurance
– 401(k)
– Vision insurance
– Life insurance
– 401(k) matching
– Flexible spending account
– Employee assistance program

About the Job

This role assists the Quality Assurance department to ensure quality products and care to customers by performing the following duties.

Essential Duties & Responsibilities

  • Review batch records for accuracy, documentation errors, completeness.
  • Review reports and logs for accuracy, documentation errors, completeness.
  • Deviations, Complaints, Out of Specification investigation and reporting. Trending of data for each to ensure overall compliance with regulatory standards.
  • Preventative Maintenance and Calibration program scheduling and management.
  • Assist with continuous staff training on cGMP to enhance the quality culture.
  • Training on other quality policies and procedures as implemented.
  • Assist in generation, review, and revision of standard operating procedures.
  • Assist in the printing and review of product labels.
  • Assist in the filing, scanning, and copying of controlled documents.
  • Ability to interpret federal and state regulatory policies and procedures.
  • Ability to perform technical writing required for SOPs and non-conformance investigation.
  • All other tasks as assigned by the Quality Assurance Management.

Supervisory Responsibilities

None

Qualifications

  • To perform this job successfully, an individual must be able to perform each essential duty satisfactorily while paying close attention to detail.
  • The requirements listed below are representative of the knowledge, skill, and/or ability required.
  • Reasonable accommodations may be made to enable individuals with disabilities to perform the essential functions.

Education & Experience

  • High School Diploma required
  • Associate Degree in Science or Health Care or related field or equivalent work experience (Preferred)
  • Familiar with GMP experience
  • Pharmaceutical experience, required
  • Prior experience with quality functions, aseptic techniques, GDP/GMP requirements, material release, investigation skills
  • Knowledge of cGMP principles as it pertains to 21 CFR 210, 211 and 503B regulated environments.

Apply

Schedule
8-hour shift

Benefits
– Health insurance
– Paid time off
– Dental insurance
– 401(k)
– Vision insurance
– Life insurance
– 401(k) matching
– Flexible spending account
– Employee assistance program

About the Job

This role assists the Quality Assurance department to ensure quality products and care to customers by performing the following duties.

Essential Duties & Responsibilities

  • Review batch records for accuracy, documentation errors, completeness.
  • Review reports and logs for accuracy, documentation errors, completeness.
  • Deviations, Complaints, Out of Specification investigation and reporting. Trending of data for each to ensure overall compliance with regulatory standards.
  • Preventative Maintenance and Calibration program scheduling and management.
  • Assist with continuous staff training on cGMP to enhance the quality culture.
  • Training on other quality policies and procedures as implemented.
  • Assist in generation, review, and revision of standard operating procedures.
  • Assist in the printing and review of product labels.
  • Assist in the filing, scanning, and copying of controlled documents.
  • Ability to interpret federal and state regulatory policies and procedures.
  • Ability to perform technical writing required for SOPs and non-conformance investigation.
  • All other tasks as assigned by the Quality Assurance Management.

Supervisory Responsibilities

None

Qualifications

  • To perform this job successfully, an individual must be able to perform each essential duty satisfactorily while paying close attention to detail.
  • The requirements listed below are representative of the knowledge, skill, and/or ability required.
  • Reasonable accommodations may be made to enable individuals with disabilities to perform the essential functions.

Education & Experience

  • High School Diploma required
  • Associate Degree in Science or Health Care or related field or equivalent work experience (Preferred)
  • Familiar with GMP experience
  • Pharmaceutical experience, required
  • Prior experience with quality functions, aseptic techniques, GDP/GMP requirements, material release, investigation skills
  • Knowledge of cGMP principles as it pertains to 21 CFR 210, 211 and 503B regulated environments.

Apply

Number of openings
1

Schedule
8-hour shift

Benefits
– Health insurance
– Paid time off
– Dental insurance
– 401(k)
– Vision insurance
– Life insurance
– 401(k) matching
– Flexible spending account
– Employee assistance program

About the Job

This role assists the Quality Assurance department to ensure quality products and care to customers by performing the following duties.

Essential Duties & Responsibilities

  • Review batch records for accuracy, documentation errors, completeness.
  • Review reports and logs for accuracy, documentation errors, completeness.
  • Deviations, Complaints, Out of Specification investigation and reporting. Trending of data for each to ensure overall compliance with regulatory standards.
  • Preventative Maintenance and Calibration program scheduling and management.
  • Assist with continuous staff training on cGMP to enhance the quality culture.
  • Training on other quality policies and procedures as implemented.
  • Assist in generation, review, and revision of standard operating procedures.
  • Assist in the printing and review of product labels.
  • Assist in the filing, scanning, and copying of controlled documents.
  • Ability to interpret federal and state regulatory policies and procedures.
  • Ability to perform technical writing required for SOPs and non-conformance investigation.
  • All other tasks as assigned by the Quality Assurance Management.

Supervisory Responsibilities

None

Qualifications

  • To perform this job successfully, an individual must be able to perform each essential duty satisfactorily while paying close attention to detail.
  • The requirements listed below are representative of the knowledge, skill, and/or ability required.
  • Reasonable accommodations may be made to enable individuals with disabilities to perform the essential functions.

Education & Experience

  • High School Diploma required
  • Associate Degree in Science or Health Care or related field or equivalent work experience (Preferred)
  • Familiar with GMP experience
  • Pharmaceutical experience, required
  • Prior experience with quality functions, aseptic techniques, GDP/GMP requirements, material release, investigation skills
  • Knowledge of cGMP principles as it pertains to 21 CFR 210, 211 and 503B regulated environments.

Apply

Job Title: Quality Assurance Associate
Wells Pharma
Houston, TX 77054

Type
Full-time

Number of openings
1

Schedule
8-hour shift

Benefits
– Health insurance
– Paid time off
– Dental insurance
– 401(k)
– Vision insurance
– Life insurance
– 401(k) matching
– Flexible spending account
– Employee assistance program

About the Job

This role assists the Quality Assurance department to ensure quality products and care to customers by performing the following duties.

Essential Duties & Responsibilities

  • Review batch records for accuracy, documentation errors, completeness.
  • Review reports and logs for accuracy, documentation errors, completeness.
  • Deviations, Complaints, Out of Specification investigation and reporting. Trending of data for each to ensure overall compliance with regulatory standards.
  • Preventative Maintenance and Calibration program scheduling and management.
  • Assist with continuous staff training on cGMP to enhance the quality culture.
  • Training on other quality policies and procedures as implemented.
  • Assist in generation, review, and revision of standard operating procedures.
  • Assist in the printing and review of product labels.
  • Assist in the filing, scanning, and copying of controlled documents.
  • Ability to interpret federal and state regulatory policies and procedures.
  • Ability to perform technical writing required for SOPs and non-conformance investigation.
  • All other tasks as assigned by the Quality Assurance Management.

Supervisory Responsibilities

None

Qualifications

  • To perform this job successfully, an individual must be able to perform each essential duty satisfactorily while paying close attention to detail.
  • The requirements listed below are representative of the knowledge, skill, and/or ability required.
  • Reasonable accommodations may be made to enable individuals with disabilities to perform the essential functions.

Education & Experience

  • High School Diploma required
  • Associate Degree in Science or Health Care or related field or equivalent work experience (Preferred)
  • Familiar with GMP experience
  • Pharmaceutical experience, required
  • Prior experience with quality functions, aseptic techniques, GDP/GMP requirements, material release, investigation skills
  • Knowledge of cGMP principles as it pertains to 21 CFR 210, 211 and 503B regulated environments.

Apply

Quality Assurance Associate