QA Technician

To Discuss more about this job opportunity, please reach out to Deepak Arya (LinkedIn URL - www.linkedin.com/in/deepak-arya-8a79aa22a/ ), email your updated resume at Email - deepak.arya@collabera.com . Thank you!

Pay Range:

$25 to $30 an hour.

Client Industry:

Medical Devices Contract Duration:

06 Months (Possibilities of Extension)

Job Summary:

We are seeking a QA Technician with strong experience in bioanalytical laboratory testing within a regulated healthcare or pharmaceutical environment. This role supports quality testing activities, laboratory operations, documentation review, and compliance initiatives in a fast paced setting. The ideal candidate will have hands on expertise with analytical and protein characterization techniques along with strong troubleshooting abilities. Candidates should be comfortable working independently while collaborating with laboratory and quality teams to support testing operations and process improvements. This position requires strong attention to detail, documentation accuracy, and adherence to GMP and GLP standards.

Key Responsibilities:

Perform routine bioanalytical quality testing according to approved laboratory procedures and specifications. Execute testing using SDS PAGE, Western Blot, Mass Spectrometry, HPLC, and microtiter plate methods. Review analytical data and determine conformance to quality standards and testing requirements. Support deviation investigations, documentation review, and laboratory quality activities. Maintain accurate laboratory records, testing documentation, and sample storage systems. Support laboratory inventory management and ensure equipment readiness for testing operations. Collaborate with laboratory teams and management to resolve testing issues and improve workflows. Ensure compliance with GMP, GLP, safety procedures, and laboratory quality systems. Participate in training activities and support audit readiness initiatives.

Required Qualifications:

Bachelor's degree in Science or a closely related discipline. Three to four years of laboratory or quality experience within healthcare, biotechnology, diagnostics, or pharmaceutical environments. Hands on experience with SDS PAGE, Western Blot, Mass Spectrometry, HPLC, and microtiter plate methods. Experience working within GMP and GLP regulated environments. Strong documentation, troubleshooting, and analytical skills. Excellent written and verbal communication skills.

Preferred Qualifications:

Experience with ELISA testing and stability studies. Experience supporting validations and method development activities. Exposure to laboratory systems and ERP system environments. Experience supporting diagnostic or biologics products.

Benefits:

The Company offers the following benefits for this position, subject to applicable eligibility requirements: medical insurance, dental insurance, vision insurance, 401(k) retirement plan, life insurance, long-term disability insurance, short-term disability insurance, paid parking/public transportation, (paid time , paid sick and safe time , hours of paid vacation time, weeks of paid parental leave, paid holidays annually - AS Applicable)