Christina Marra

Investigations Specialist @Regeneron

Waterford, NY, US
EMAILS
c••••••••@regeneron.com
MOBILE NUMBERS
+17•••••••79

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WORK HISTORY

Feb 2023 — Present

Investigations Specialist @Regeneron

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Independently investigating non conformances and preventing reoccurrences in support of manufacturing operations• Preparing investigation reports that include recommendations on investigation findings for medium/high severity non conformances• Analyzing and evaluating information captured through investigations, summarizes information and trends in investigation reports• Communicating findings and recommendations at group meetings• Reviewing completed batch records and logbooks in accordance with cGMP standards in support of investigations• Reviewing, editing, and revising controlled documents (batch records, logbooks, SOPs, etc.) in accordance with cGMP standards to ensure compliance with written procedures• Monitoring production processes to acquire vital data in support of investigations and track efficiency of changes• Participating in and/or leading cross-functional study teams to get results, support and or author investigations• Gathering, trending, and analyzing process related data to drive consistency and timeliness• Documenting all training• Training new employees on investigative processes and techniques• Coordinating and/or leading cross-functional meetings with multiple departments

EDUCATION

2010 — 2013

Cazenovia College

Bachelor's of Professional Studies in Business Management (B.P.S), Business Management/Marketing

SKILLS

MarketoCommunity OutreachEvent PlanningMarketing StrategyInterviewing SkillsTime ManagementSocial MediaMicrosoft OfficeMarketingEmail MarketingLeadershipCustomer ServiceTalent SelectionManagementPowerpointMicrosoft ExcelFacebookSocial Networking

ABOUT CHRISTINA MARRA

As an investigations specialist at Regeneron, I apply my bachelor\'s degree in business management and my extensive experience in quality assurance and operations management to ensure compliance and prevent reoccurrences of non conformances in manufacturing operations. I am proficient in preparing investigation reports, analyzing and evaluating information, communicating findings and recommendations, and reviewing and revising controlled documents in accordance with cGMP standards.In my current role, I independently investigate medium/high severity non conformances, using Concept 4 electronic data collection methods, and provide solutions to improve the quality and efficiency of the production process. I am motivated by the opportunity to contribute to the development and delivery of life-saving medicines, and to bring diverse perspectives and experiences to the team. I value allyship, social networking, and high performance, and I continuously seek to enhance my skills and knowledge in these areas.

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