Flow Cytometry QC Associate 1

Manpower San Diego; San Diego (CA); On-site; USD 50,000 - 80,000; Full time

Job summary

An established industry player is seeking a QC Associate I to join their quality assurance team. This role involves performing routine testing of QC samples, ensuring compliance with standard protocols, and maintaining accurate documentation. The ideal candidate will have a background in flow cytometry and tissue culture, along with strong analytical skills. You will work independently while prioritizing daily tasks, contributing to a safe and efficient laboratory environment. Join a dynamic team where your contributions will directly impact the quality of medical equipment manufacturing.

Qualifications

• Minimum 2 years experience in a biotech lab environment.
• Flow Cytometry experience required; Tissue Culture preferred.

Responsibilities

• Perform routine QC tests and maintain accurate documentation.
• Analyze data and report results according to protocols.
• Promote a safe work environment and participate in safety programs.

Skills

Flow Cytometry

Tissue Culture

Analytical Skills

Problem-Solving

Interpersonal Communication

Computer Skills (MS Excel & Word)

Education

BA/BS in a related scientific discipline

Related college coursework

Tools

Laboratory Equipment

Database Software

Job description

Must have: Previous flow cytometry experience and BA/BS degree in a related scientific discipline or some related college coursework with a minimum of 2 years’ experience in a biotech lab environment.

The QC Associate I is responsible for routine, accurate and timely testing of QC samples according to standard protocols and operating procedures, such as flow cytometry related protocols. The QC Associate I will prioritize daily workload and work independently. They will participate in the review of data, report results, and complete all required documentation and database entries. QC Associate I will receive specific instructions and ongoing guidance regarding required tasks and expected results.

JOB RESPONSIBILITIES

1. Trains and becomes proficient in all the required techniques, operation of relevant equipment and software packages associated with testing, data analysis, and data reporting.
2. This may require working with human blood, human or mammalian cell culture and/or animals and animal tissues.
3. Routine, accurate and timely completion of all assigned QC tests under supervision and according to standard protocols or operating procedures.
4. Will prioritize daily workload and develop skills to work independently.
5. Analyze data and report test results including completion of all required documentation and database entries as required by QC protocols or operating procedures.
6. Calibrate and maintain equipment. Report problems to QC Supervisor or Manager.
7. Maintain logs and required documentation, as necessary.
8. Prepare lab supplies, reagents, and assist with laboratory maintenance, as needed.
9. Promote a safe work environment. May provide recommendations on maintaining the safety of the work environment.
10. Participate in Environmental, Health & Safety programs.
11. Address corrective actions whenever a hazard is identified.
12. Notify supervisor and Safety Officer(s) of all observed hazardous conditions or unsafe work practices.
13. Keep abreast of the basic requirements for safety compliance in own area of work and complies with those requirements.
14. Participate in group or intra-department teams and projects as required.
15. Participate in assigned cross-training.
16. Perform other related duties and assignments, as required.

EDUCATION AND EXPERIENCE:

1. BS/BA in a related scientific discipline or some related college coursework with a minimum of 2 years related experience in a biotech lab environment.
2. Experience in an industrial or research laboratory preferred.
3. Flow Cytometry experience required and Tissue Culture experience highly preferred.

KNOWLEDGE AND SKILLS

1. Basic computer skills: MS Excel & Word.
2. Knowledge of general laboratory safety.
3. Effective interpersonal, written and oral communication skills.
4. Demonstrated ability to follow established policies/procedures, and ability to keep neat, accurate, and complete records and logs.
5. Effective analytical and problem-solving skills.

Seniority level

Associate

Employment type

Full-time

Job function

Quality Assurance

Industries

Medical Equipment Manufacturing