Lisandra Ortiz Email & Phone Number
@catalent.com
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Who is Lisandra Ortiz? Overview
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Lisandra Ortiz is listed as QA Compliance Specialist at Merck, a with 8864 employees, based in Greater Tampa Bay Area, United States. AeroLeads shows a work email signal at catalent.com and a matched LinkedIn profile for Lisandra Ortiz.
Lisandra Ortiz previously worked as QA Manager at Catalent Pharma Solutions and Sr. QA Technical Reviewer at Catalent Pharma Solutions. Lisandra Ortiz holds Bachelor Degree, Natural Sciences, Physics Applied To Electronics from University Of Puerto Rico.
Email format at Merck
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AeroLeads found 1 current-domain work email signal for Lisandra Ortiz. Compare company email patterns before reaching out.
About Lisandra Ortiz
Professional with extensive experience in Pharmaceutical, Cosmetics, Medical Devices and Molding Industry. Experience in quality inspections and systems, manufacturing and packing processes. Accountable, self-managed, highly ethical, self-starter and fast learner in a high quality regulated environment. Proven leadership, problem solving and good negotiation skills. Proven ability to define problems, collect data, establish facts, and draw valid conclusions. Ability to work with little or no supervision, exercise professional judgment and follow policies, procedures and law requirements. Manage a high-volume workload within a deadline in a constantly changing environment. Certified Quality Auditor (CQA) by ASQ.
Listed skills include Documentation, Quality Assurance, Pharmaceutical Industry, Beauty Industry, and 25 others.
Lisandra Ortiz's current company
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Lisandra Ortiz work experience
A career timeline built from the work history available for this profile.
Qa Manager
Current
Sr. Qa Technical Reviewer
Qa Group Leader
Qa Specialist
Quality Assurance
Quality Supervisor
• Supervised, coached and educated Quality Inspectors, Technicians and Incoming personnel on systems and procedures. • Took necessary containment measures for quality issues reported and ensure required standards are sustained. • Documented and investigated process deviations and discrepancies.• Approved Nonconformance’s investigations and manage rejected material according to its disposition.• Worked closely with cross-functional departments to resolve issues and ensure quality… Show more • Supervised, coached and educated Quality Inspectors, Technicians and Incoming personnel on systems and procedures. • Took necessary containment measures for quality issues reported and ensure required standards are sustained. • Documented and investigated process deviations and discrepancies.• Approved Nonconformance’s investigations and manage rejected material according to its disposition.• Worked closely with cross-functional departments to resolve issues and ensure quality standards are in place.• Approved master batch records and product specifications, as required. • Supported new products introduction and validations.• Responsible of developing, collecting, maintain, trending and analyzing data for Quality metrics and present it to senior site and corporate management. • Actively participated in external and internal audits. • CAPA owner, responsible of time closure of records. • Wrote, reviewed and approved GMP’s documents such as SOPs, Quality Plans, and Work Instructions among others. Show less
Member Of The Career Transition Support Team
Quality Assurance Technician
• Supported external audits (FDA) and internal audits. • Evaluate packing materials for conformity to specifications and records inspections results. • Generated Nonconformance documentation and supported the investigation. • Reviewed and approved the required documentation for packing material (e.g.: “Certificate of Compliance “COA”, Certificate of Analysis “COC”).
Qa Document Control Specialist
• Audited manufacturing and packing documents to ensure that documents are in place and in compliance. • Responsible for distribution/notification of QA form releases, changes and obsolescence.• Provided training as required on Good Documentation Practices.• Administrated the cGMP Logbook System at the plant.• Wrote and reviewed Standard Operational Procedures (SOPs) as needed.• Received and maintained control and tracking of documents according to its lifecycle.… Show more • Audited manufacturing and packing documents to ensure that documents are in place and in compliance. • Responsible for distribution/notification of QA form releases, changes and obsolescence.• Provided training as required on Good Documentation Practices.• Administrated the cGMP Logbook System at the plant.• Wrote and reviewed Standard Operational Procedures (SOPs) as needed.• Received and maintained control and tracking of documents according to its lifecycle. • Participated in the company internal audits (Self Improvement Program).• Audited Olay’s products in stores during the Annual Trade Survey. Show less
Quality Functional Leader
• Leaded the quality performance of the line before, during and after the packing process. • Monitored quality of finished products by performing visual inspections and measure variables.• Received and verified that packing components are precise and in compliance. • Generated Nonconformance documentation and supported the investigation. • Issued packing batch records according to the Packing Instructions and SOP’s. • Performed the reconciliation of all materials and… Show more • Leaded the quality performance of the line before, during and after the packing process. • Monitored quality of finished products by performing visual inspections and measure variables.• Received and verified that packing components are precise and in compliance. • Generated Nonconformance documentation and supported the investigation. • Issued packing batch records according to the Packing Instructions and SOP’s. • Performed the reconciliation of all materials and Finished Products.• Reviewed batch records prior to be submitted to Quality Release for final approval. • Approved the cleaning and sanitization process at the assigned area. Show less
Ehs Specialist / Utilities Operator
Colleagues at Merck
Other employees you can reach at catalent.com. View company contacts for 8864 employees →
Nicolás Santos
Colleague at MerckBuenos Aires, Buenos Aires Province, Argentina
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SM
Sara Miller
Colleague at MerckKansas City, Missouri, United States
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SC
Saundra Corbin-Woods
Colleague at MerckPiscataway, New Jersey, United States
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ZA
Zachary Avent
Colleague at MerckUnited States
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JB
Jaws Bel K
Colleague at MerckBrussels Metropolitan Area, Belgium
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Naresh Neupane
Colleague at MerckUnited States
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HS
Hannah Smith
Colleague at MerckOverland Park, Kansas, United States
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MB
Marive Bustos
Colleague at MerckUnited States
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AC
Amanda Chowdri
Colleague at MerckBloomington, Indiana, United States
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Camryn Livingston
Colleague at MerckBloomington, Indiana, United States
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Lisandra Ortiz education
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University Of Puerto Rico
Frequently asked questions about Lisandra Ortiz
Quick answers generated from the profile data available on this page.
What company does Lisandra Ortiz work for?
Lisandra Ortiz works for Merck.
What is Lisandra Ortiz's role at Merck?
Lisandra Ortiz is listed as QA Compliance Specialist at Merck.
What is Lisandra Ortiz's email address?
AeroLeads has found 1 work email signal at @catalent.com for Lisandra Ortiz at Merck.
Where is Lisandra Ortiz based?
Lisandra Ortiz is based in Greater Tampa Bay Area, United States while working with Merck.
What companies has Lisandra Ortiz worked for?
Lisandra Ortiz has worked for Merck, Catalent Pharma Solutions, Nestlé Waters, Nypro, A Jabil Company, and Procter & Gamble.
Who are Lisandra Ortiz's colleagues at Merck?
Lisandra Ortiz's colleagues at Merck include Nicolás Santos, Sara Miller, Saundra Corbin-Woods, Zachary Avent, and Jaws Bel K.
How can I contact Lisandra Ortiz?
You can use AeroLeads to view verified contact signals for Lisandra Ortiz at Merck, including work email, phone, and LinkedIn data when available.
What schools did Lisandra Ortiz attend?
Lisandra Ortiz holds Bachelor Degree, Natural Sciences, Physics Applied To Electronics from University Of Puerto Rico.
What skills is Lisandra Ortiz known for?
Lisandra Ortiz is listed with skills including Documentation, Quality Assurance, Pharmaceutical Industry, Beauty Industry, Packing, Special Events Coordination, Auditing, and Visual Inspection.
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