Quality Control (QC) Associate I

Valid8 Financial, Inc.; San Diego (CA); On-site; USD 28,000 - 33,000; Full time

Benefits offered by this job

Medical/Dental insurance

Onsite gym

Wellness perks

Company holidays

Job summary

Aspen Neuroscience, Inc. in Torrey Pines, CA is seeking a QC Associate I to support cGMP manufacturing through sampling and testing of raw materials, intermediates, drug product and stability samples.

You will participate in environmental monitoring and ensure data integrity in a fast-paced on-site lab. Responsibilities include material inspection, EM sampling in aseptic environments, lab organization, calibration, and investigations of deviations.

Qualifications

• Attention to detail and organizational skills: Exceptional ability to manage tasks efficiently and maintain high levels of accuracy.
• Proficiency in Microsoft software: Demonstrated experience with Microsoft Office Suite and other Microsoft applications.
• Initiative in a dynamic environment: Strong self-starter with the ability to thrive in a fast-paced setting.
• Teamwork and independence: Capable of collaborating effectively within a team and working independently after initial training.
• Communication skills: Excellent written and verbal communication abilities.
• Flexibility: Willingness to work flexible hours, including occasional weekends, to support production needs.
• Knowledge of GMP Regulations: Basic familiarity with Good Manufacturing Practices (GMP) and industry standards

Responsibilities

• Perform raw material inspection and sampling.
• Perform EM sampling in aseptic manufacturing environments: total particulate monitoring, active air sampling, surface and personnel monitoring.
• Assist with submission of samples to contract testing laboratories.
• Assist with organizing QC laboratories including equipment calibration.
• Conduct QC tests for raw material, intermediates, drugproductand stability samples.
• Perform test following test protocols and procedures in compliance with quality standards and cGMP regulationsapplicable to QC laboratory.
• Deliver cGMP compliant testing data and reports.
• Participate in investigation of deviation or out-of-specification results in QC laboratory.

Skills

Attention to detail

Organizational skills

Proficiency in Microsoft Office

Initiative

Teamwork and independence

Communication skills

Flexibility

Knowledge of GMP Regulations

Education

B.S. in Biology/Cell Biology/Microbiology/ Biochemistry

Tools

Microsoft Office Suite

Job description

The Quality Control (QC) Associate I will contribute to general QC operations and testing in support of current Good Manufacturing Practice (cGMP) manufacturing for an innovative cell and gene therapy program. This individual will participate in Environmental Monitoring (EM), raw material, intermediates, drug product, and stability testing program. This is an on-site role in Torrey Pines, CA that requires flexibility and availability for weekend and holiday work as needed. Relocation is not available.

DUTIES AND RESPONSIBILITIES

• Perform raw material inspection and sampling.
• Perform EM sampling in aseptic manufacturing environments: total particulate monitoring, active air sampling, surface and personnel monitoring.
• Assist with submission of samples to contract testing laboratories.
• Assist with organizing QC laboratories including equipment calibration.
• Conduct QC tests for raw material, intermediates, drugproductand stability samples.
• Perform test following test protocols and procedures in compliance with quality standards and cGMP regulationsapplicable to QC laboratory.
• Deliver cGMP compliant testing data and reports.
• Participate in investigation of deviation or out-of-specification results in QC laboratory.

EDUCATION AND EXPERIENCE

• B.S.Degree in Biology, Cell Biology, Microbiology, Molecular Biology or Biochemistry; Or equivalentrelevanteducation and experience.
• Experience working inalaboratory(academic or industry)settingand within a cGMP regulated environment ispreferred.

JOB SPECIFICATIONS

• Attention to detail and organizational skills:Exceptional ability to manage tasks efficiently and maintain high levels of accuracy.
• Proficiency in Microsoft software:Demonstrated experience with Microsoft Office Suite and other Microsoft applications.
• Initiative in a dynamic environment:Strong self-starter with the ability to thrive in a fast-paced setting.
• Teamwork and independence:Capable of collaborating effectively within a team and working independently after initial training.
• Communication skills:Excellent written and verbal communication abilities.
• Flexibility: Willingness to work flexible hours, including occasional weekends, to support production needs.
• Knowledge of GMP Regulations:Basic familiarity with Good Manufacturing Practices (GMP) and industry standards

WORKING CONDITIONS

Office and Lab environment. While performing the duties of this Job, the employee is frequently exposed to toxic or caustic chemicals. This is an indoor position requiring the ability to perform experiments in the laboratory, and type and use a computer.

May work in Cleanroom for an extended period of time.

PHYSICAL DEMANDS

While performing the responsibilities of the job, the employee is occasionally required to stand, walk, reach with arms and hands, climb or balance, and to stoop, kneel, crouch, or crawl. The physical effort required is sedentary,liftingupto 10 pounds.

The noise level in the work environment is usually quiet to moderate. The passage of employees through the work area is average and normal.

These work environment characteristics are representative of the environment the job holder will encounter. Reasonableaccommodationsmay be made to enable people with disabilities to perform the essential functions of the job.

EEO and Employment Eligibility

Aspen Neuroscience is committed to providing equal employment opportunities to all employees and job applicants and prohibits discrimination and harassment of any type. We are committed to creating an inclusive environment for all employees. Aspen is not able to provide visa sponsorship for this role. Applicants must have valid work authorization that does not require employer sponsorship now or in the future.

Total Rewards and Culture

Aspen Neuroscience, Inc., located in scenic Torrey Pines, is noted for its collaborative and learning focused culture where each person is valued for contributing their strengths and energy to building a world-class line of products for patients in need. The company offers a competitive total compensation package, time-off in addition to Company observed holidays, Medical/Dental insurance benefits, onsite gym, and other wellness perks.

The anticipated salary range for candidates who will work in San Diego is $28.00 -$33.00 annually. The final salary offered to a successful candidate will be dependent on several factors that may include but are not limited to the type and length of experience within the industry, education, etc. Aspen Neuroscience is multi-state employer, and this salary range may not reflect positions that work in other states.