
Job Overview
Employment Type
Temporary
Compensation
Hourly
Range $23.00 - $31.00
Work Schedule
Standard Hours
Benefits
Medical insurance
Dental Insurance
Paid holidays
Paid Time Off
401K Matching
Job Description
The hiring organization is a renowned global leader in eye care, committed to enhancing people's vision and overall eye health worldwide. With decades of experience and a passion for innovation, this company has established itself as the world's largest vision care provider. Their dedication extends beyond providing products — it encompasses advancing eye care science through research, technology, and quality assurance in every aspect of their operations. Headquartered in Fort Worth, TX, the company combines cutting-edge technology with a commitment to sustainability and employee development, making them an excellent choice for those seeking a meaningful career in the health sciences sector.
This opportunity is for a Quality Control Analyst I position within their state-of-the-art laboratory environment. This role is designed for entry-level candidates or those early in their quality control careers seeking to grow professionally in a highly regulated and dynamic setting. The position is a 12-month contract with extension or conversion potential, offering competitive pay ranging from $24.00 to $26.00 per hour, depending on experience. Additionally, the role comes with generous benefits including medical and dental coverage, paid holidays, paid time off (PTO), and 401K matching.
As a Quality Control Analyst I, you will play a vital role in ensuring the quality and safety of the eye care products through meticulous laboratory testing and quality operations. This includes performing routine and non-routine analytical tests on raw materials, in-process samples, and finished goods, ensuring adherence to strict quality standards and regulatory requirements. Your expertise will contribute to product quality by interpreting test results accurately, maintaining thorough and precise documentation, calibrating and troubleshooting laboratory equipment, and supporting method validation and continuous improvement efforts.
The role also involves collaborating closely with cross-functional teams to support deviations, out-of-specification (OOS) investigations, corrective actions, and regulatory compliance initiatives. You will assist in writing and revising standard operating procedures (SOPs), protocols, and technical reports, thus ensuring that laboratory practices remain at the forefront of industry standards. By supporting audits and regulatory inspections, you help maintain the company’s reputation for excellence and quality compliance.
This position is ideal for professionals who hold a bachelor's degree in Chemistry, Biology, or related scientific disciplines and have at least one year of experience in a QC or analytical laboratory setting. Familiarity with Good Manufacturing Practices (GMP) or working in a regulated environment is highly desirable. Strong documentation skills, effective troubleshooting abilities, and clear communication are essential attributes for success in this role.
Overall, this Quality Control Analyst I role offers an exceptional platform for career development within a world-leading company dedicated to eye health innovation. It is not only a job but a chance to contribute to a meaningful mission with real impact on people's lives globally. Join this esteemed team to build your expertise, work with advanced technologies, and grow within a supportive, forward-thinking organization.
This opportunity is for a Quality Control Analyst I position within their state-of-the-art laboratory environment. This role is designed for entry-level candidates or those early in their quality control careers seeking to grow professionally in a highly regulated and dynamic setting. The position is a 12-month contract with extension or conversion potential, offering competitive pay ranging from $24.00 to $26.00 per hour, depending on experience. Additionally, the role comes with generous benefits including medical and dental coverage, paid holidays, paid time off (PTO), and 401K matching.
As a Quality Control Analyst I, you will play a vital role in ensuring the quality and safety of the eye care products through meticulous laboratory testing and quality operations. This includes performing routine and non-routine analytical tests on raw materials, in-process samples, and finished goods, ensuring adherence to strict quality standards and regulatory requirements. Your expertise will contribute to product quality by interpreting test results accurately, maintaining thorough and precise documentation, calibrating and troubleshooting laboratory equipment, and supporting method validation and continuous improvement efforts.
The role also involves collaborating closely with cross-functional teams to support deviations, out-of-specification (OOS) investigations, corrective actions, and regulatory compliance initiatives. You will assist in writing and revising standard operating procedures (SOPs), protocols, and technical reports, thus ensuring that laboratory practices remain at the forefront of industry standards. By supporting audits and regulatory inspections, you help maintain the company’s reputation for excellence and quality compliance.
This position is ideal for professionals who hold a bachelor's degree in Chemistry, Biology, or related scientific disciplines and have at least one year of experience in a QC or analytical laboratory setting. Familiarity with Good Manufacturing Practices (GMP) or working in a regulated environment is highly desirable. Strong documentation skills, effective troubleshooting abilities, and clear communication are essential attributes for success in this role.
Overall, this Quality Control Analyst I role offers an exceptional platform for career development within a world-leading company dedicated to eye health innovation. It is not only a job but a chance to contribute to a meaningful mission with real impact on people's lives globally. Join this esteemed team to build your expertise, work with advanced technologies, and grow within a supportive, forward-thinking organization.
Job Requirements
- bachelor's degree in chemistry biology or related science
- minimum 1 year of qc or analytical laboratory experience
- familiarity with gmp or regulated laboratory environments preferred
- strong written and verbal communication skills
- ability to troubleshoot and maintain laboratory equipment
- attention to detail and accuracy in documentation
- ability to work collaboratively in a team environment
Job Qualifications
- bachelor's degree in chemistry biology or related science
- 1+ years of qc or analytical lab experience
- experience in a gmp or regulated environment preferred
- strong documentation troubleshooting and communication skills
Job Duties
- perform routine and non-routine testing of raw materials in-process samples and finished goods
- interpret test results and ensure compliance with specifications and quality standards
- maintain accurate lab documentation logbooks and test records
- calibrate and troubleshoot laboratory equipment
- support method validation method transfer and continuous improvement activities
- assist with deviations out-of-specification investigations and corrective actions
- write and revise standard operating procedures protocols and technical reports
- support audits regulatory compliance and cross-functional quality initiatives
Job Criteria
Experience
Entry Level (1-2 years)
Job Location
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