Specialist Qa - Juncos, Puerto Rico - Qrc Group, Llc

Specialist Qa

hace 4 días

Specialist QA with experience in: Aseptic Technics Change ControlNew Product IntroductionRequisitos:Doctorate degree or Master's degree and 3 years of directly related experience orBachelor's degree and 5 years of directly related experience (Education: Science or Engineering)Bil ...

Specialist QA

hace 1 semana

Job Description · Specialist QA with experience in regulated industries to: · Perform Trackwise system queries, deviations · Participate in triage process · Perform oversight of the process and procedures/GMP tasks · Manage Change Controls and deviations for review and approval a ...

Specialist Qa

hace 1 semana

Specialist QA with experience in regulated industries to:Perform Trackwise system queries, deviationsParticipate in triage processPerform oversight of the process and procedures/GMP tasksManage Change Controls and deviations for review and approval as QA contactWork with operatio ...

Specialist QA

hace 1 semana

Job Description · Specialist QA with experience in regulated industries to:Perform Trackwise system queries, deviations · Participate in triage process · Perform oversight of the process and procedures/GMP tasks · Manage Change Controls and deviations for review and approval as Q ...

Specialist QA

hace 1 semana

Specialist QA with experience in regulated industries to:Perform Trackwise system queries, deviations · Participate in triage process · Perform oversight of the process and procedures/GMP tasks · Manage Change Controls and deviations for review and approval as QA contact · Work w ...

Specialist QA

hace 21 horas

Kelly Science & Clinical is seeking Specialist QA for contract position at Pharmaceutical client in Puerto Rico East area. · FUNCTIONS · - Review and approve product MPs. · - Approve process validation protocols and reports for manufacturing processes. - Request Quality on incid ...

Specialist Manufacturing

hace 21 horas

Kelly Engineering is seeking Specialist Manufacturing for a 12 month contract position at a Global Pharmaceutical & Biotechnology client in Juncos, Puerto Rico. If you're passionate about bringing the latest scientific discoveries to life and are ready to take the next step in yo ...

QA Specialist

hace 4 días

Expertise required: · Aseptic Techniques, Change Control and New Product Introduction. · Requirements · Education and years of experience requirements; · Doctorate degree or Master's degree and 3 years of directly related experience · or Bachelor's degree and 5 years of directly ...

Specialist QA

hace 1 semana

Candidates qualifications / expertise; · • Perform Trackwise system queries, deviations · • Participate in triage process · • Perform oversight of the process and procedures/GMP tasks · • Manage Change Controls and deviations for review and approval as QA contact · • Work with op ...

Specialist Manufacturing

hace 21 horas

Project need expertise required;Procedure development · Change Control · CAPA · Deviation · Risk Assessment · Requirements · Shift, Education & years of experience needed;Doctorate degree OR Master's degree and 3 years of Manufacturing Operations experience · OR Bachelor's degre ...

Specialist Manufacturing

hace 1 día

Job Description · Project need expertise required;Procedure development · Change Control · CAPA · Deviation · Risk Assessment · Requirements · Shift, Education & years of experience needed;Doctorate degree OR Master's degree and 3 years of Manufacturing Operations experience · O ...

Specialist QA

hace 13 horas

mirus Consulting Group is a local company based in Humacao, Puerto Rico that provides computer system validation and information technology consulting services to pharmaceutical companies and other organizations across the Island and parts of the United States. Its services inclu ...

QA Specialist

hace 1 semana

Job Description · Expertise required: · Aseptic Techniques, Change Control and New Product Introduction. · Requirements · Education and years of experience requirements; · Doctorate degree or Master's degree and 3 years of directly related experience · or Bachelor's degree and 5 ...

Specialist QA

hace 1 día

SUMMARY · Perform one or more of the following duties and responsibilities in support of Client's Quality Assurance program under minimal supervision. · FUNCTIONS · - Review and approve product MPs. · - Approve process validation protocols and reports for manufacturing processes. ...

Specialist QA

hace 4 días

Job Description · Candidates qualifications / expertise; · • Perform Trackwise system queries, deviations · • Participate in triage process · • Perform oversight of the process and procedures/GMP tasks · • Manage Change Controls and deviations for review and approval as QA contac ...

Engineering Specialist

hace 4 días

· Minimum Requirements · Mid-level individual contributor on a project or work team, 3-5 years of experience required. · Bachelor Degree in Engineering · Experience within Medical Devices and/or Pharmaceutical industries. · Experience in equipment IQ, OQ and PQ, Validation, CSV ...

Specialist Qa

hace 5 días

For Quality services in the Quality Assurance area WHAT MAKES YOU A FIT: The Technical Part: Bachelor's Degree with five (5) years of directly experience as Quality Professional in the regulated industry. Bilingual (English & Spanish) Project Management skills Shift: Administrati ...

Qa Specialist

hace 6 días

Perform one or more of the following duties and responsibilities in support of Quality Assurance program under minimal supervision.Requisitos:Preferred Qualifications: · • Perform Trackwise system queries, deviations · • Participate in triage process · • Perform oversight of the ...

Specialist QA

hace 1 semana

Qualified candidates please review the required expertise; · • Perform Trackwise system queries, deviations · • Participate in triage process · • Perform oversight of the process and procedures/GMP tasks · • Manage Change Controls and deviations for review and approval as QA cont ...

Specialist Qa

hace 3 días

Functions: - Review and approve product MPs. - Approve process validation protocols and reports for manufacturing processes. - Request Quality on incident triage team.- Approve Environmental Characterization reports.- Release of sanitary utility systems.- Approve planned incident ...