Associate Director
Current
Dec 2022 - Present
AeroLeads people directory · profile
Anna Celeste Alonzi Email & Phone Number
Associate Director, Regulatory Affairs CMC
at
Novavax
1 work email found
@novavax.com
LinkedIn matched
✓ Verified July 2026
4 data sources
Profile completeness 100%
Current company
Role
Associate Director, Regulatory Affairs CMC
Location
Greater Philadelphia, United States
Who is Anna Celeste Alonzi? Overview
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Quick answer
Anna Celeste Alonzi is listed as Associate Director, Regulatory Affairs CMC at Novavax, based in Greater Philadelphia, United States. AeroLeads shows a work email signal at novavax.com and a matched LinkedIn profile for Anna Celeste Alonzi.
Anna Celeste Alonzi previously worked as Associate Director at Novavax and Senior Manager, Regulatory Affairs CMC at Novavax. Anna Celeste Alonzi holds Regulatory Affairs Certificate: Pharmaceuticals from Rapsonline University.
Company email context
Email format at Novavax
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{first_initial}{last}@novavax.com
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Profile bio
About Anna Celeste Alonzi
Experienced Senior Regulatory with a demonstrated history of working in the biotechnology industry (oncology, immunology, large and small molecules, vaccines). Skilled in CMC Regulatory Affairs, Supplements, Annual Report, IND/CTA, BLA, MA, cmc, Change Control, Biotechnology, U.S. Food and Drug Administration (FDA), EMA, Global submissions. Corrective and Preventive Action (CAPA). RAPSOnline University: Pharmaceuticals certificate.
Listed skills include Gmp, Regulatory Affairs, Pharmaceutical Industry, Regulatory Submissions, and 24 others.
Current workplace
Anna Celeste Alonzi's current company
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13 roles · 27 years
Anna Celeste Alonzi work experience
A career timeline built from the work history available for this profile.
Senior Manager, Regulatory Affairs Cmc
Current
Oct 2021 - Present
Gra Cmc Reg Affairs Associate
Jun 2020 - Oct 2021
Sr. Regulatory Associate-Biologics
Senior Regulatory Associate in PTR: responsibility for post-approval submissions (AR, CBE-30, PAS, Type I and II) of biologics in compliance with applicable regulations and guidelines. Main activities: Authoring, review and adjudication of regulatory submissions (US, EU, Canada, Japan, RoW) of biologics. Ability to work across the globe with different time zones and global stakeholders. Change control assessor at global level.
Feb 2016 - Feb 2020
Volunteer
Sep 2013 - Jun 2016
Process Engineer
APR/QPR of solids and combination products in Compliance Operation Department.
Oct 2015 - Jan 2016
Operation Investigation Supervisor
Senior Engineer in J&J:DeviationInvestigationCAPA
Aug 2014 - 2015
Regulatory (Operation)
Haupt -Aenova Group
Haupt PharmaManaged CMC regulatory affairs of “Animal Health” areaSupervised quality/regulatory relationship with the customers Change control system owner
Jan 2012 - Aug 2014
Gmp And Regulatory Compliance (Operation)
In charge of all CMC regulatory topics including New Product Introduction. Managed regulatory affairs of Human Health areaSupervised quality/regulatory relationship with the customers Change control system owner
Jan 2009 - Dec 2011
Ah Regional Regulatory
Managed regulatory issues of veterinary section in collaboration withcorporate regulations as a member of the “Regulatory Compliance Team”. Managed the following CMC activities:- renewals,- variations,- new submissions,- deficiency letters.
Oct 2006 - Jan 2009
Environmental Monitoring, Unit Team Leader
Supervised environmental monitoring in a 10-member microbiologicallaboratory team, consisting of 11 sterile production lines and 5 oral production lines managing the following activities:- Investigations (write and approval)- CAPA management- SOP writing- Quality Reports- Environmental Monitoring Validation- Identification (Vitek system)- Regulatory audit- Training on analysts and production operators- Air, surface and operators microbiological control
Oct 2004 - Sep 2006
Environmental Monitoring Supervisor
Supervised a 23-member microbiological laboratory in a sterileproduction site, managing the following activities:- Investigations (write and approval)- CAPA lab management- SOP writing- Quality Reports- Environmental Monitoring Validation- Identification (Vitek system)- Regulatory audits- Training on analysts and production operators- Air, surface and operators microbiological control- Member of the sterility assurance team- Regulatory audit
Apr 2003 - Oct 2004
Researcher In Biotechnology
Biotechnology researcher in a Biotech Company producing large molecules by fermentation process. Activities:- Monitoring of the process- Collecting of sample during fermentation process- Collecting sample during purification process- SDS-page- Western blotting- Elisa- Bio-Rad assay- UV techniques- All chromatographic techniques
2000 - 2003
~3 yrs
6 education records
Anna Celeste Alonzi education
Regulatory Affairs Certificate: Pharmaceuticals
Rapsonline University
Master Level Ii, Stress And Nutrition
La Sapienza
Master, Nutrition
Istituto Alta Formazione
Education record
Aaps Member
Laurea, Scienze Biologiche
Università Degli Studi Dell'Aquila
Education record
Liceo Classico Torlonia
FAQ
Frequently asked questions about Anna Celeste Alonzi
Quick answers generated from the profile data available on this page.
What company does Anna Celeste Alonzi work for?
Anna Celeste Alonzi works for Novavax.
What is Anna Celeste Alonzi's role at Novavax?
Anna Celeste Alonzi is listed as Associate Director, Regulatory Affairs CMC at Novavax.
What is Anna Celeste Alonzi's email address?
AeroLeads has found 1 work email signal at @novavax.com for Anna Celeste Alonzi at Novavax.
Where is Anna Celeste Alonzi based?
Anna Celeste Alonzi is based in Greater Philadelphia, United States while working with Novavax.
What companies has Anna Celeste Alonzi worked for?
Anna Celeste Alonzi has worked for Novavax, Eli Lilly And Company, Genentech, Vacaville Christian Schools, and Johnson & Johnson.
How can I contact Anna Celeste Alonzi?
You can use AeroLeads to view verified contact signals for Anna Celeste Alonzi at Novavax, including work email, phone, and LinkedIn data when available.
What schools did Anna Celeste Alonzi attend?
Anna Celeste Alonzi holds Regulatory Affairs Certificate: Pharmaceuticals from Rapsonline University.
What skills is Anna Celeste Alonzi known for?
Anna Celeste Alonzi is listed with skills including Gmp, Regulatory Affairs, Pharmaceutical Industry, Regulatory Submissions, Quality Assurance, Fda, Biotechnology, and Sop.
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