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Ivan Mesnil Email & Phone Number
Director of Quality Assurance - BioPharma Compliance
at
Eurofins BioPharma Product Testing North America
1 work email found
@eurofinsus.com
5 phones found area 787, 256, and 484
LinkedIn matched
✓ Verified Jun 2026
4 data sources
Profile completeness 100%
Current company
Role
Director of Quality Assurance - BioPharma Compliance
Location
Greater Philadelphia, United States, United States
Who is Ivan Mesnil? Overview
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Quick answer
Ivan Mesnil is listed as Director of Quality Assurance - BioPharma Compliance at Eurofins BioPharma Product Testing North America, based in Greater Philadelphia, United States, United States. AeroLeads shows a work email signal at eurofinsus.com, phone signal with area code 787, 256, 484, and a matched LinkedIn profile for Ivan Mesnil.
Ivan Mesnil previously worked as Senior Manager Quality Assurance - Biologics Manufacturing Facility at Teva Pharmaceuticals and Quality Assurance Manager at Teva Pharmaceuticals. Ivan Mesnil holds Bachelor'S Degree, Biochemistry And Molecular Biology from University Of Massachusetts Amherst.
Company email context
Email format at Eurofins BioPharma Product Testing North America
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{first}{last}@eurofinsus.com
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AeroLeads found 1 current-domain work email signal for Ivan Mesnil. Compare company email patterns before reaching out.
Profile bio
About Ivan Mesnil
Quality Operations professional with more than 20 years of proven history of success leading Quality Operations in the pharmaceutical industry. Experience with oral solid dose, injectable, surgical/medical device and biotechnology industries combined, in addition to CMO/CRO service provider. Proven results in scheduling, FDA, EMA, and TGA audits readiness., cycle-time, and department metrics. Extensive technical knowledge, people management skills and hands-on approach in building teams to achieve high level of quality and compliance.- Knowledge of FDA, GxP, ICH, and ISO regulations and industry best practices.- Strong Leadership, team building, and communication skills more than 20 years of direct supervision experience and leading teams.- Customer/Stakeholder focused (understands business plans and operating environment).- Ability to organize, prioritize work in the face of shifting demands and tight deadlines.- Detailed oriented, able to work independently and work well in a team environment.- Demonstrated understanding of continuous improvement methodologies including Lean, Six Signa, SPC, etc.- Clear problem-solving and de decision-making skills- Strong written and verbal communication skills and the ability to effectively communicate with internal and external personnel at all levels of the organization as required.- Experience in technical writing, protocols, test methods, executive summaries and non-conformance investigations.- Support Risk Management
Listed skills include Fda, Capa, Gmp, Change Control, and 33 others.
Current workplace
Ivan Mesnil's current company
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Eurofins Biopharma Product Testing North America
AeroLeads page
8 roles
Ivan Mesnil work experience
A career timeline built from the work history available for this profile.
Director Of Quality Assurance - Biopharma Compliance
CurrentOversee and facilitate operations and systems in accordance with company policies and quality systems. Ensure that the quality policy/program is understood, implemented, and maintained at all levels of the organization. Drive on-time completion of Quality Metrics to 100% Facilitate periodic meetings with different department management teams to discuss.
Jul 2020 - Present
Senior Manager Quality Assurance - Biologics Manufacturing Facility
Responsibilities have expanded to include QA oversight of all Biologics Manufacturing activities related to facilities, validation and implementation of process improvements to the overall investigations, CAPA and change control programs. Assumed responsibility for oversight of the Vendor and Raw Materials Management programs, and Supplier Quality.
Mar 2019 - Jul 2020
Quality Assurance Manager
a. Assist with development of new program for raw materials for the future production facility, prepare vendor files, coordinate vendor questionnaires and audits, and maintain approved vendor’s list. Work with the Manufacturing group for their change controls relating to raw materials and consumables. Work with Manufacturing and Quality Control for.
Aug 2016 - Mar 2019
Qa Operations Manager
- Manage QA personnel and provide final QA disposition of batches manufactured. Provide or supervise final QA approval of non-conformance investigations and disposition of any product batches affected.
- Expertise with deviations metrics and CAPA; primary source of department investigations
- Manages and prioritizes workloads and projects to ensure effective and efficient completion of departmental objectives.
- Main auditor and approver for all Packaging deviations, NCR, CAPA in Trackwise. In charge of the approval of QC laboratory OOS on behalf of the Site QA Director.
- Third Party Quality internal audits support.
- Quality Agreements review and approval.
Jan 2010 - Jun 2016
Sr. Analyst Process Quality Assurance
- Audit the manufacturing and packaging processes to assure compliance with cGMP's and Work Instructions.
- Review the batch record to include data entries on the batch record, performing necessary signoffs and second checks, reconciliation during the manufacturing and packaging of each production batch and ensures all.
- Coordinate the completion of all documentation/ steps to complete the disposition process. At the time of disposition enters status and if needed correct expiration dating in SAP.
- Experience in new products, protocols, MBR’s, characterization, stability and clinical trial runs.
- Executes the transfer and start-up of new existing products to be manufactured in the plant, through trials runs and /or transferred products, and generates training documentation.
- Generate and upgrade manufacturing documents (mfg. Instructions, SOPs, etc.) in full compliance with process design and specifications, GMPs and company policies.
Oct 2008 - Dec 2009
Quality Manager
Omj Pharmaceuticals Inc. / Johnson & Johnson
- Operations team member. Coordinated efforts and projects with manufacturing areas
- Conducted laboratory investigations and analytical related technical assessments.
- Participated in internal audits, regulatory agencies Inspections as analytical technical expert.
- Support of R&D and Regulatory Compliance activities that included test method transfers, improve current product quality testing, developmental studies for submissions, etc.
- Executed approvals of raw materials, in-process, finished products and stability tests.
- Served as quality management representative and supported the execution of key quality system elements, including QN/CAPA, management review, and regulatory inspection readiness activities.
Jan 2006 - Nov 2007
Sr. Qc Supervisor
Ortho Biologics Llc. / Johnson & Johnson
- Supported CSM (Critical System Modification) regarding test methods and analytical laboratory instrumentation.
- Support of R&D and Process Development new product launch EVRB, coordinated all testing requirements, and approval of data results for the validation protocols.
- 14 reports. Supported management during FDA and European (EMEA) agency audits.
- Coordinated activities related to laboratory instrumentation remediation plan for Part 11 compliance.
- Key member for Ortho Biologics Manati Laboratories expansion project (2004-05) completion. Full implementation of LIMS (Laboratory Information Management System) at the Manati site.
Sep 2000 - Dec 2005
2 education records
Ivan Mesnil education
Bachelor'S Degree, Biochemistry And Molecular Biology
University Of Massachusetts Amherst
Master Of Business Administration (Mba), Business Administration And Management, General
University Of Phoenix
FAQ
Frequently asked questions about Ivan Mesnil
Quick answers generated from the profile data available on this page.
What company does Ivan Mesnil work for?
Ivan Mesnil works for Eurofins BioPharma Product Testing North America.
What is Ivan Mesnil's role at Eurofins BioPharma Product Testing North America?
Ivan Mesnil is listed as Director of Quality Assurance - BioPharma Compliance at Eurofins BioPharma Product Testing North America.
What is Ivan Mesnil's email address?
AeroLeads has found 1 work email signal at @eurofinsus.com for Ivan Mesnil at Eurofins BioPharma Product Testing North America.
What is Ivan Mesnil's phone number?
AeroLeads has found 5 phone signal(s) with area code 787, 256, 484 for Ivan Mesnil at Eurofins BioPharma Product Testing North America.
Where is Ivan Mesnil based?
Ivan Mesnil is based in Greater Philadelphia, United States, United States while working with Eurofins BioPharma Product Testing North America.
What companies has Ivan Mesnil worked for?
Ivan Mesnil has worked for Eurofins Biopharma Product Testing North America, Teva Pharmaceuticals, Par Pharmaceutical, The Janssen Pharmaceutical Companies Of Johnson & Johnson, and Omj Pharmaceuticals Inc. / Johnson & Johnson.
How can I contact Ivan Mesnil?
You can use AeroLeads to view verified contact signals for Ivan Mesnil at Eurofins BioPharma Product Testing North America, including work email, phone, and LinkedIn data when available.
What schools did Ivan Mesnil attend?
Ivan Mesnil holds Bachelor'S Degree, Biochemistry And Molecular Biology from University Of Massachusetts Amherst.
What skills is Ivan Mesnil known for?
Ivan Mesnil is listed with skills including Fda, Capa, Gmp, Change Control, Pharmaceutical Industry, Sop, 21 Cfr Part 11, and Validation.
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