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Jobs

CALTEK is all about our people. We ensure that the

work is engaging, our culture is empowering and

the learning opportunities are enriching.

​

If this sounds good to you, join us.

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Upload your Resume here

Current Job Opportunities

Software Developer (Ref:5):

Research, analyze, design, develop and test the solutions that are appropriate for the business and technology strategies.

Participate in design discussions and project-related team meetings.

Partner with other developers, product managers, QA, analysts, and operations teams to deliver scalable, fault-tolerant solutions.

Practice and improve industry standard methodologies, such as ci/cd, test automation, a/b testing, and experimentation.

Monitor and test newly implemented applications for reliability, security, and performance.

Develop automated tests and deliver high-quality software code to production within a short development cycle in the continuous integration and delivery environment.

 

Tools: Java, JSON, Jenkins, SOAP, Couchbase.

 

Minimum Education: Master’s in Computer Science, Information Systems Technologies or a related field

 

Minimum experience: Two (2) years

 

Position requires two (2) years of experience, which must include two (2) years of experience in Java, JSON, Jenkins, SOAP, Couchbase.

 

Job Site: 3910 Lake Arrowhead Ave, Suite A, Fremont, CA 94555.

 

Pay Range: $155,605-165,605/year

 

Please send resumes referencing the aforementioned job title and reference number to Caltek Solutions, Inc., 3910 Lake Arrowhead Ave, STE A, Fremont, CA 94555 or by email to hrm@caltek.us

Quality Control Systems Manager

Quality Control Systems Manager

 

CALTEK Solutions Inc., headquartered at 3910 Lake Arrowhead Avenue, Suite A, Fremont, CA 94555 seeks to hire a Quality Control Systems Manager

 

Job duties will include:

 

  • Deviation management through DCMS(Deviation and CAPA management system)

  • Tracking and review of CAPAs related to the audit observations.

  • Assigning, tracking, review and approval of OOS (Out of Specification), OOT (Out of trend), Deviation, CAPA reports.

  • Review and approval of electronic Master batch records (e-MBR) in MES(Manufacturing execution system)

  • Review and release of executed electronic batch records (e-BR) in PAS-X by WERUM 3.1.8 Version.

  • Review and approval of change comparison sheets.

  • Preparation of reduced testing / skip testing justification reports with the statistical evaluation of batch data using MINITAB.

  • Performing GAP Analysis and initiation of change controls where ever required.

  • Monitoring the process of manufacturing, cGMP compliance and dispatch activities.

  • Review and approval of product recipe creation protocols.

  • Review of Machine generated prints such as Audit Trail Reports Event reports &DAS (DATA ACQUISITION SYSTEM) reports.

  • Review and approval of electronic user management requests for GxP applications and standalone equipment.

 

Education: Bachelor’s degree in Pharmaceutical Sciences or related

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