Cqa Wilberto Algarin-Lopez wilberto.algarin-lopez@gilead.com & | I have extensive experience within the quality control and regulatory environment as well as experience with domestic and international regulatory inspections. I specialize in HPLC, Raw Materials management, method validation and method transfer following current requirements established by pharmacopoeia and ICH guidelines. Throughout my career I have held leadership positions within the laboratory environment such as workflow (floor) manager, supervisor and multi-site method validation/method transfer coordinator. I have a strong laboratory safety discipline and extensive knowledge about office and laboratory ergonomics as demonstrated by my involvement in the development of job hazards assessments and injury prevention. Qualifications Summary •Bachelors Degree in Science - Industrial Chemistry; University of Puerto Rico. •Outstanding technical laboratory experience (>20 years) in the areas of Raw Materials and HPLC within GMP and GLP environments. •Experience with method development, validation and transfer. •Experience with redaction and revision of analytical methods and standard operation procedures (SOP). •Strong leadership skills. •Experience with laboratory management, team building and process improvement. •Experience with laboratory investigations, root cause analysis and corrective and preventive action (CAPA) analysis. •Strong laboratory instrumentation background. •Familiarity with compendia methods (USP, EP, JP) and ICH requirements. •Good communications skills in English and Spanish. •Computer skills; Microsoft Word, Excel, Power Point presentations, Trackwise and specialized laboratory software (LIMS, CDS/EMPOWER, CIMS, LMES). •Ability to work with minimal supervision.

Cqa Wilberto Algarin-Lopez

I have extensive experience within the quality control and regulatory environment as well as experience with domestic and...

United States

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Cqa Wilberto Algarin-Lopez’s Emails [email protected]

Cqa Wilberto Algarin-Lopez’s Phone Numbers No phone number available.

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Cqa Wilberto Algarin-Lopez’s Location United States

Cqa Wilberto Algarin-Lopez’s Expertise I have extensive experience within the quality control and regulatory environment as well as experience with domestic and international regulatory inspections. I specialize in HPLC, Raw Materials management, method validation and method transfer following current requirements established by pharmacopoeia and ICH guidelines. Throughout my career I have held leadership positions within the laboratory environment such as workflow (floor) manager, supervisor and multi-site method validation/method transfer coordinator. I have a strong laboratory safety discipline and extensive knowledge about office and laboratory ergonomics as demonstrated by my involvement in the development of job hazards assessments and injury prevention. Qualifications Summary •Bachelors Degree in Science - Industrial Chemistry; University of Puerto Rico. •Outstanding technical laboratory experience (>20 years) in the areas of Raw Materials and HPLC within GMP and GLP environments. •Experience with method development, validation and transfer. •Experience with redaction and revision of analytical methods and standard operation procedures (SOP). •Strong leadership skills. •Experience with laboratory management, team building and process improvement. •Experience with laboratory investigations, root cause analysis and corrective and preventive action (CAPA) analysis. •Strong laboratory instrumentation background. •Familiarity with compendia methods (USP, EP, JP) and ICH requirements. •Good communications skills in English and Spanish. •Computer skills; Microsoft Word, Excel, Power Point presentations, Trackwise and specialized laboratory software (LIMS, CDS/EMPOWER, CIMS, LMES). •Ability to work with minimal supervision.

Cqa Wilberto Algarin-Lopez’s Current Industry Biomarin Pharmaceutical

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Work Experience

Biomarin Pharmaceutical

Associate Director

Sun May 01 2022 00:00:00 GMT+0000 (Coordinated Universal Time) — Present

Mile High Labs

Analytical Laboratory Manager

Fri Jan 01 2021 00:00:00 GMT+0000 (Coordinated Universal Time) — Sun May 01 2022 00:00:00 GMT+0000 (Coordinated Universal Time)

Agilent Technologies

QC Supervisor

Fri Dec 01 2017 00:00:00 GMT+0000 (Coordinated Universal Time) — Fri Jan 01 2021 00:00:00 GMT+0000 (Coordinated Universal Time)

Gilead Sciences

Team Lead QC PDM

Mon Jun 01 2015 00:00:00 GMT+0000 (Coordinated Universal Time) — Wed Nov 01 2017 00:00:00 GMT+0000 (Coordinated Universal Time)

Amgen

Quality Control Specialist

Sun Mar 01 2009 00:00:00 GMT+0000 (Coordinated Universal Time) — Mon Dec 01 2014 00:00:00 GMT+0000 (Coordinated Universal Time)

Amgen

QC Manager - HPLC Laboratory

Mon May 01 2006 00:00:00 GMT+0000 (Coordinated Universal Time) — Sun Mar 01 2009 00:00:00 GMT+0000 (Coordinated Universal Time)

Amgen

QC Manager - Raw Materials Laboratory

Tue Apr 01 2003 00:00:00 GMT+0000 (Coordinated Universal Time) — Mon May 01 2006 00:00:00 GMT+0000 (Coordinated Universal Time)

Astrazeneca

Analytical Development Group Analyst

Sun Jul 01 2001 00:00:00 GMT+0000 (Coordinated Universal Time) — Tue Apr 01 2003 00:00:00 GMT+0000 (Coordinated Universal Time)

Searle

Laboratory Technician / Laboratory Process Flow Assurer

Fri Apr 01 1994 00:00:00 GMT+0000 (Coordinated Universal Time) — Tue May 01 2001 00:00:00 GMT+0000 (Coordinated Universal Time)

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Languages

FAQ About Cqa Wilberto Algarin-Lopez

Cqa Wilberto Algarin-Lopez is located at
United States

Cqa Wilberto Algarin-Lopez is a
I have extensive experience within the quality control and regulatory environment as well as experience with domestic and international regulatory inspections. I specialize in HPLC, Raw Materials management, method validation and method transfer following current requirements established by pharmacopoeia and ICH guidelines. Throughout my career I have held leadership positions within the laboratory environment such as workflow (floor) manager, supervisor and multi-site method validation/method transfer coordinator. I have a strong laboratory safety discipline and extensive knowledge about office and laboratory ergonomics as demonstrated by my involvement in the development of job hazards assessments and injury prevention. Qualifications Summary •Bachelors Degree in Science - Industrial Chemistry; University of Puerto Rico. •Outstanding technical laboratory experience (>20 years) in the areas of Raw Materials and HPLC within GMP and GLP environments. •Experience with method development, validation and transfer. •Experience with redaction and revision of analytical methods and standard operation procedures (SOP). •Strong leadership skills. •Experience with laboratory management, team building and process improvement. •Experience with laboratory investigations, root cause analysis and corrective and preventive action (CAPA) analysis. •Strong laboratory instrumentation background. •Familiarity with compendia methods (USP, EP, JP) and ICH requirements. •Good communications skills in English and Spanish. •Computer skills; Microsoft Word, Excel, Power Point presentations, Trackwise and specialized laboratory software (LIMS, CDS/EMPOWER, CIMS, LMES). •Ability to work with minimal supervision. Biomarin Pharmaceutical

Cqa Wilberto Algarin-Lopez currently works in the
Biomarin Pharmaceutical

Cqa Wilberto Algarin-Lopez specializes in
I have extensive experience within the quality control and regulatory environment as well as experience with domestic and international regulatory inspections. I specialize in HPLC, Raw Materials management, method validation and method transfer following current requirements established by pharmacopoeia and ICH guidelines. Throughout my career I have held leadership positions within the laboratory environment such as workflow (floor) manager, supervisor and multi-site method validation/method transfer coordinator. I have a strong laboratory safety discipline and extensive knowledge about office and laboratory ergonomics as demonstrated by my involvement in the development of job hazards assessments and injury prevention. Qualifications Summary •Bachelors Degree in Science - Industrial Chemistry; University of Puerto Rico. •Outstanding technical laboratory experience (>20 years) in the areas of Raw Materials and HPLC within GMP and GLP environments. •Experience with method development, validation and transfer. •Experience with redaction and revision of analytical methods and standard operation procedures (SOP). •Strong leadership skills. •Experience with laboratory management, team building and process improvement. •Experience with laboratory investigations, root cause analysis and corrective and preventive action (CAPA) analysis. •Strong laboratory instrumentation background. •Familiarity with compendia methods (USP, EP, JP) and ICH requirements. •Good communications skills in English and Spanish. •Computer skills; Microsoft Word, Excel, Power Point presentations, Trackwise and specialized laboratory software (LIMS, CDS/EMPOWER, CIMS, LMES). •Ability to work with minimal supervision.

Cqa Wilberto Algarin-Lopez speaks the following languages:
No languages available.

Cqa Wilberto Algarin-Lopez has prior experience in the following industries:
Mile High Labs , Agilent Technologies , Gilead Sciences , Amgen , Amgen , Amgen , Astrazeneca , Searle

Cqa Wilberto Algarin-Lopez has the following professional experience:
Biomarin Pharmaceutical , Mile High Labs , Agilent Technologies , Gilead Sciences , Amgen , Amgen , Amgen , Astrazeneca , Searle .