Joaquin Davila Email & Phone Number |  Working knowledge of highly regulated environments, Pharmaceutical: Solids and Chemical Bulk/API.  Strong background in GMP documentation including Investigations, Protocols, and Standard Operational Procedures.  Skilled at organizing complex projects, defining project priorities, and delegating tasks. Self-motivated and assertive.  Exercise initiative, achievement and independent judgment.  Able to direct and lead others to produce desired results.  Direct Participation in FDA Audits management, Consent Decree and Remediation projects in several GMP facilities.  Ethically driven, excellent interpersonal, leadership and technical writing skills.  Computer literate with strong knowledge of MS Office, LIMS, Trackwise, Minitab, Graphic Software, EtQ, and SAP.  Fully Bilingual. Areas of Expertise:  QUALITY SYSTEMS:  Change Control  Standard Operating Procedures  Investigations  CAPA  Annual Product Reviews (APR's)  Laboratory Systems  SME Excel databases and programming SPECIALIZED TRAINING:  GMP  Statistical Process Control  Trackwise  Technical Writing  Cleaning Validation  Method Validation  Industrial Validation

Joaquin Davila

 Working knowledge of highly regulated environments, Pharmaceutical: Solids and Chemical Bulk/API....
Guayama, Guayama, Puerto Rico

*50 free lookup(s) per month.

Joaquin Davila’s Email jdavila@jnj.com

Joaquin Davila’s Phone Numbers +1 609-730-****

Get JOAQUIN’s Phone Number (For Free)

Social Media

Joaquin Davila’s Location Guayama, Guayama, Puerto Rico

Joaquin Davila’s Current Industry Teva Pharm The Janssen Pharmaceutical Companies Of Johnson And Johnson

Joaquin Davila’s Prior Industry Mcneil Consumer Healthcare | Searle

Find accurate emails & phone numbers for over 700M professionals.

Quality Assurance Engineer

Present

Compliance Investigator Technologist

2017-01-01 00:00:00 - Present

Sr. Qa Specialist-Puerto Rico, Ptsprocesstech

2015-03-01 00:00:00 - Present

Investigation Metrics

2011-01-01 00:00:00 - 2015-01-01 00:00:00

Chemist

1992-01-01 00:00:00 - 1996-01-01 00:00:00

No Skills Available

No Languages Available

Joaquin Davila is a  Working knowledge of highly regulated environments, Pharmaceutical: Solids and Chemical Bulk/API.  Strong background in GMP documentation including Investigations, Protocols, and Standard Operational Procedures.  Skilled at organizing complex projects, defining project priorities, and delegating tasks. Self-motivated and assertive.  Exercise initiative, achievement and independent judgment.  Able to direct and lead others to produce desired results.  Direct Participation in FDA Audits management, Consent Decree and Remediation projects in several GMP facilities.  Ethically driven, excellent interpersonal, leadership and technical writing skills.  Computer literate with strong knowledge of MS Office, LIMS, Trackwise, Minitab, Graphic Software, EtQ, and SAP.  Fully Bilingual. Areas of Expertise:  QUALITY SYSTEMS:  Change Control  Standard Operating Procedures  Investigations  CAPA  Annual Product Reviews (APR's)  Laboratory Systems  SME Excel databases and programming SPECIALIZED TRAINING:  GMP  Statistical Process Control  Trackwise  Technical Writing  Cleaning Validation  Method Validation  Industrial Validation

Joaquin Davila currently works in the Teva Pharm | The Janssen Pharmaceutical Companies Of Johnson And Johnson |

Joaquin Davila has prior
experience in the following industries:
Mcneil Consumer Healthcare | Searle

Joaquin Davila has the following professional experience:
Medtronic | Teva Pharm | The Janssen Pharmaceutical Companies Of Johnson And Johnson | Mcneil Consumer Healthcare | Searle