Mary Climo

Senior Manager Quality Systems

We found the following information about Mary Climo at Mei Pharma, where Mary has worked as a Senior Manager Quality Systems since 2019. Mary's total work experience is over 28 years, during which time this expert had at least five jobs at different places to develop professional skills. Mary Climo studied at the Cypress College. Corona, California is the place where this person currently lives. You can contact with Mary by searching for phone or email address or get further information by requesting access to this professional's details.
Name variants:
Maria Climo, Marie Climo, Mare Climo, Mame Climo, Mamie Climo, Mimi Climo, Moll Climo, Molly Climo, Polly Climo, Mae Climo, May Climo, Mollie Climo, Minnie Climo
Last updated Jun 01, 2024

Contact Information

Last Update
Jul 6, 2022
Email
ma**@yahoo.com, cl**@allergan.com
Location
Corona, CA
Company

Workplace

MEI Pharma
Senior Manager Quality Systems

San Diego, CA

Industry

Biotechnology, Mfg Pharmaceutical Preparations, Pharmaceutical Preparations

Work History

Senior Manager Quality Systems

3611 Valley Centre Dr, San Diego, CA 92130
Maintaining and execution of systems and processes to ensure compliance with GxP regulations, including Clinical Trials. Providing quality guidance to meet company goals and objectives. K...
from May 2019

Senior Manager, Corporate Internal Audits Global Inspections and Audits

Serve as Lead Auditor for Company sites, subsidiaries, and suppliers for compliance to GxP including serialization and Data Integrity. Lead a team of auditors, overseeing workflow, complia...
Aug 2016 — Apr 2019

Corporate Compliance Manager

Trained auditors on compliance and standard operating procedures; managed daily workflow and responded to escalated issues. Reviewed companies’ systems, documentation, and training procedu...
Jan 2000 — Aug 2016

Associate Director of Quality Assurance and Regulatory Affairs

Spearheaded initiation and approval of standard operating procedures and validated employee training systems. Audited Contact Research Organizations, API suppliers, vivariums, pharmacovigi...
1995 — 1999

Quality Assurance

ADDITIONAL WORK HISTORY Quality Assessment Specialist, Alcon Laboratories Quality Assurance Supervisor, Steri-Oss Receiving Inspection Lead, Beckman
1989 — 1994

Education

Occupations

Executive
Senior Manager
Accountant
Auditor
Operations Manager

Skills

Fda
Gmp
Regulatory Affairs
Quality System
Pharmaceutical Industry
21 Cfr Part 11
Quality Assurance
Change Control
Anda
Sop
Pharmaceutics
Aseptic Processing
Deviations
Gxp
Trackwise
Regulatory Submissions
Glp
Validation
Regulatory Requirements
Computer System Validation
Technology Transfer
Quality Auditing
Lims
Cleaning Validation
Software Documentation
Iso
Biopharmaceuticals
Corrective and Preventive Action
Gamp
Iso Standards
U.s. Food and Drug Administration
Usp
Dietary Supplements
Good Clinical Practice
Medical Devices
Clinical Trials
Research and Development
Pharmacovigilance
Biotechnology
Quality Management
Microsoft Office
Cross Functional Team Leadership
Leadership
Data Integrity
Serialization
International Regulations
Combo Products
Quality Control
Capa
V&V
Fda Gmp
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