Ricardo Rivera

Ricardo Rivera Email and Phone Number

Executive Director Manufacturing, Clinical Supply Operations at Bristol Myers Squibb @ Bristol Myers Squibb
Ricardo Rivera's Location
United States, United States
Ricardo Rivera's Contact Details

Ricardo Rivera personal email

n/a

Ricardo Rivera phone numbers

About Ricardo Rivera

• Pharmaceuticals professional with over 20 years of experience with leadership roles at global, regional and manufacturing site level• Subject Matter Expert in Technology Transfers, New Product Launches, Validation, Project Management and Product Lifecycle Management• Technical responsibility throughout my career over non-sterile (i.e. tablets, capsules, liquids, others) and sterile (i.e. vials, syringes) products/processes.• Vast experience collaborating with Contract Manufacturing Organizations and supporting Business Development and Licensing deals• Proven leadership designing, implementing and optimizing a technical organization

Ricardo Rivera's Current Company Details
Bristol Myers Squibb

Bristol Myers Squibb

View
Executive Director Manufacturing, Clinical Supply Operations at Bristol Myers Squibb
Ricardo Rivera Work Experience Details
  • Bristol Myers Squibb
    Executive Director Clinical Manufacturing
    Bristol Myers Squibb Nov 2023 - Present
    Lawrence Township, Nj, Us
    View
  • Bristol Myers Squibb
    Senior Director Manufacturing, Clinical Supply Operations
    Bristol Myers Squibb Sep 2020 - Nov 2023
    Lawrence Township, Nj, Us
    View
  • Bristol Myers Squibb
    Director Manufacturing, Clinical Supply Operations
    Bristol Myers Squibb Nov 2018 - Sep 2020
    Lawrence Township, Nj, Us
    View
  • Novartis
    Director, Manufacturing Science And Technology
    Novartis Sep 2016 - Nov 2018
    Basel, Baselstadt, Ch
    • Establish strategic goals and objectives and maintain full strategic responsibility for the MSAT organization.• As a site leadership team member, drive collaboration within site and across network activities, cross-functional planning, and decision making.• Accountable for overall budget and financial performance of the MSAT organization.• Direct areas of responsibility: Validation, Technology Transfer, Process Engineering, Packaging Process Engineering and Manufacturing Support.
    View
  • Sandoz
    Director, Manufacturing Science And Technology, External Supply Operations
    Sandoz Apr 2014 - Aug 2016
    Basel, Basel-Stadt, Ch
    • Created and led the new Manufacturing Science and Technology organization for Americas External Supply Operations. • Developed and implemented MSAT systems to ensure end-to-end oversight of drug products (sterile and non-sterile) at all stages of the commercial lifecycle.• Developed and implemented the technical requirements, responsibilities and processes for Business Development and Licensing deals.
    View
  • Novartis Consumer Health
    Global Head Of Manufacturing Science And Technology - Third Party Operations
    Novartis Consumer Health Jul 2012 - Apr 2014
    Basel, Baselstadt, Ch
    • Created and led the new Manufacturing Science and Technology Organization for the Global Third Party Organization (25 engineers/scientists; 5 locations: US, Switzerland, India, Brazil, Mexico).• Developed and implemented MSAT systems to ensure end-to-end oversight of drug products at all stages of the commercial lifecycle.• Developed and implemented a global approach for Product Quality Assessments of products manufactured by Contract Manufacturing Organizations.
    View
  • Novartis Consumer Health
    Head Of Global Technical Services A.I.
    Novartis Consumer Health Jun 2011 - Jul 2012
    Basel, Baselstadt, Ch
    • Led the Global Technical Services organization responsible for identifying and executing changes to commercialized OTC products (i.e. product transfers, changes to raw materials, minor formulation changes, optimizing manufacturing processes, etc.) ensuring compliance thru the lifecycle of the product and delivering COGs savings to the business.• Managed a team of 5 engineers located in the US and Europe.• Responsible for defining and optimizing work processes and systems, building organization capability, developing individuals and ensuring the organization delivers its annual targets.• Led the Product Quality Assessment (PQA) Work-stream for the Americas Third Party Operations Region.• Managed a team of up to 25 consultants executing PQA at Contract Manufacturing Organizations. Defined the process and protocols, served as single point of contact for Contract Manufacturing Organizations and led remediation discussion with QA.
    View
  • Novartis Consumer Health
    Manager, Global Mfg Technical Support
    Novartis Consumer Health Jun 2007 - Jul 2011
    Basel, Baselstadt, Ch
    • Managed the technology transfer of marketed products to Contract Manufacturing Organizations for the Latin America Region.• Project leader, project manager and technical resource of product transfers. Responsible for developing the technology transfer strategy (process validation, stability requirements, regulatory, logistic, etc.) and putting together the project team (Supply Chain, Regulatory Affairs, Quality, Contract Operations, Planning, Text & Design, etc).• Identified Contract Manufacturing Organizations, negotiated COGS, performed technical Due Diligence and provided Receiving Site recommendation to Global Manufacturing and Supply.
    View
  • Pfizer
    Manager, Consumer Products Support
    Pfizer Jun 2004 - Jun 2007
    New York, New York, Us
    • Member of the new products Co-Development (Multi-Disciplinary) team representing Pfizer Global Manufacturing.• Co-led with R&D the technology transfer of new products from pilot plant to Contract Manufacturing Organizations.• Led activities to solve technical issues at manufacturing sites. Led process validation activities. Responsible for compiling and reviewing all compliance documentation of new products. Reviewed and approved changes to marketed products from the technical point of view.• Led six sigma projects to improve marketed products• I worked for McNeil Consumer during the last 6 months of this job. Pfizer sold it Consumer Division to J&J in November 2016.
    View
  • Pfizer
    Senior Technical Services Technologist
    Pfizer Jan 2002 - May 2004
    New York, New York, Us
    • Receiving site project leader for the technology transfer of new Rx products. Liaison between the manufacturing site, R&D and external contractors.• Coordinated the execution of experimental, ICH stability and commercial batches.• Performed qualification of new equipment (IQ, OQ, PQ and cleaning validation). • Provided technical support to Engineering Department during the design phase of the new manufacturing area for a new product.
    View
  • Pfizer
    Senior Technical Specialist / Technical Specialist
    Pfizer Mar 1999 - Jan 2002
    New York, New York, Us
    • Process improvement team leader, member and coach; i.e. yield improvements, optimization of production schedule, new technology, etc.• Evaluated and implemented new tableting technology for bi-layer and single layer tablets. • Site subject matter expert troubleshooting tablet presses; i.e. capping, sticking, etc.• Developed and executed validation protocols.• Performed investigations due to GMP deviations and implemented CAPA to avoid recurrence.
    View
  • Pfizer
    Manufacturing Supervisor
    Pfizer May 1997 - Mar 1999
    New York, New York, Us
    • Supervised a manufacturing shift of approximately 20 operators.• Responsible for day-to-day operations including indirect supervision of In-process QC and Engineering personnel assigned to production.• Developed and executed validation protocols. Generated investigations / CAPA due to GMP deviations and implemented recommendations to avoid recurrence.
    View
  • Pfizer
    Project Engineer
    Pfizer Nov 1996 - May 1997
    New York, New York, Us
    • Executed commissioning activities of a new chemical plant.
    View
  • Consulting Firm
    Validation Engineer
    Consulting Firm Oct 1995 - Oct 1996
    • Developed and executed installation and operational qualification protocols for auxiliary equipment on a chemical plant.

Ricardo Rivera Skills

Gmp Validation Pharmaceutical Industry Technology Transfer Capa Quality System Fda Change Control

Ricardo Rivera Education Details

  • Universidad De Puerto Rico
    Universidad De Puerto Rico
    Chemical Engineering

Frequently Asked Questions about Ricardo Rivera

What company does Ricardo Rivera work for?

Ricardo Rivera works for Bristol Myers Squibb

What is Ricardo Rivera's role at the current company?

Ricardo Rivera's current role is Executive Director Manufacturing, Clinical Supply Operations at Bristol Myers Squibb.

What is Ricardo Rivera's email address?

Ricardo Rivera's email address is ri****@****ast.net

What is Ricardo Rivera's direct phone number?

Ricardo Rivera's direct phone number is +41 61 324 *****

What schools did Ricardo Rivera attend?

Ricardo Rivera attended Universidad De Puerto Rico.

What skills is Ricardo Rivera known for?

Ricardo Rivera has skills like Gmp, Validation, Pharmaceutical Industry, Technology Transfer, Capa, Quality System, Fda, Change Control.

Free Chrome Extension

Find emails, phones & company data instantly

Find verified emails from LinkedIn profiles
Get direct phone numbers & mobile contacts
Access company data & employee information
Works directly on LinkedIn - no copy/paste needed
Get Chrome Extension - Free

Aero Online

Your AI prospecting assistant

Download 750 million emails and 100 million phone numbers

Access emails and phone numbers of over 750 million business users. Instantly download verified profiles using 20+ filters, including location, job title, company, function, and industry.