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Santina Spera Email & Phone Number
Senior Quality Control Chemistry Analyst
at
BeOne Medicines
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✓ Verified Jul 2026
3 data sources
Profile completeness 86%
Current company
Role
Senior Quality Control Chemistry Analyst
Location
Philadelphia, Pennsylvania, United States
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Who is Santina Spera? Overview
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Quick answer
Santina Spera is listed as Senior Quality Control Chemistry Analyst at BeOne Medicines, a with 1970 employees, based in Philadelphia, Pennsylvania, United States. AeroLeads shows a matched LinkedIn profile for Santina Spera.
Santina Spera previously worked as Raw Material Analyst at Beigene and Quality Control Manager at Lannett Company, Inc.. Santina Spera holds Master Of Science - Ms, Pharmaceutical Sciences from Temple University.
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Email format at BeOne Medicines
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BeOne Medicines
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Profile bio
About Santina Spera
With over 15 years of experience in the pharmaceutical industry, I am an accomplished Quality Control Manager with a Master of Science in Pharmaceutical Sciences. I have a proven track record of leading and training a diverse team of laboratory professionals in conducting complex analyses, validating methods, and documenting data in compliance with GMP regulations. At Lannett Company, Inc., I leveraged my expertise in analytical techniques, quality standards, and laboratory management to ensure the highest level of product quality and customer satisfaction. I achieved significant milestones in my career, such as improving audit performances, overseeing and completing FDA audits across multiple sites, enhancing product quality, and streamlining laboratory operations. I also collaborated with cross-functional teams to maintain project progress and resolve issues efficiently. I am looking for opportunities to use my skills and knowledge to contribute to your organization's success and to work with teams that share my dedication to excellence and innovation.
Current workplace
Santina Spera's current company
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Beone Medicines
6 roles
Santina Spera work experience
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Raw Material Analyst
Quality Control Manager
Jun 2020 - Dec 2023
Raw Materials Group Leader
Trained new team members by relaying information on company procedures and safety requirements. Reviewed daily requirements and forecasts and delegated work for optimal production release time to adhere to production schedule. Collaborated with cross-functional teams to maintain project progress. Reviewed method validation and method transfer protocols and reports. Oversaw group of seven, delegated tasks strategically, and monitored progress for timely completion of a variety of API's and excipients. Developed and implemented performance monitoring systems to track team progress. Resolved conflict quickly to limit operational disruption and maintain positive, productive working environments. Used problem-solving and issue-resolution skills to promptly and successfully address production problems. Completed inventory and destruction for DEA Controlled Substances.
Jan 2018 - Jun 2020
Quality Control Scientist
• Documented changes during experiments, noting unexpected issues arising during laboratory activities. Conducted laboratory experiments in cGMP environment for product release purposes and documented in real-time, following cGMP procedures. Primarily operated HPLC for complex analyses, while also performing some basic troubleshooting. Engaged in instrument maintenance and basic troubleshooting of GC, serving as one of persons responsible for in-house calibration of GC instruments. Analyzed laboratory samples on HPLC, UPLC, and GC on daily basis, resolving unusual data trends and handling chromatography and instrument alarms as appropriate. Conducted moderately complex analysis to support product release. Simultaneously managed several complex projects, meeting all pertinent milestones and deadlines. Authored and executed testing for various method validation protocols and reports based on USP monograph updates. Conducted various raw material analyses simultaneously while maintaining quality output with minimal error and deviation, demonstrating excellent right-first-time statistics.
Sep 2010 - Jan 2018
Quality Control Lab Analyst
Prepared samples for analysis by performing various levels of sample solution preparation, including wet chemistry techniques such as titration, TLC analysis, and Karl Fischer analysis. Analyzed raw material, in-process, and finished product clinical samples on GC, HPLC, UPLC instruments using Empower and ChemStation software. Performed laboratory testing in environment compliant with GMP, FDA, DEA, and OSHA regulations. Thoroughly communicated with fellow team members to ensure they had accurate information for any ongoing analyses during shift change.
Oct 2008 - Sep 2010
4 education records
Santina Spera education
Master Of Science - Ms, Pharmaceutical Sciences
Bachelor Of Arts - Ba, Chemistry
Bachelor'S Degree, Chemistry
Bachelor'S Degree, Chemistry
FAQ
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What company does Santina Spera work for?
Santina Spera works for BeOne Medicines.
What is Santina Spera's role at BeOne Medicines?
Santina Spera is listed as Senior Quality Control Chemistry Analyst at BeOne Medicines.
Where is Santina Spera based?
Santina Spera is based in Philadelphia, Pennsylvania, United States while working with BeOne Medicines.
What companies has Santina Spera worked for?
Santina Spera has worked for Beone Medicines, Beigene, Lannett Company, Inc., and Noramco™.
How can I contact Santina Spera?
You can use AeroLeads to view verified contact signals for Santina Spera at BeOne Medicines, including work email, phone, and LinkedIn data when available.
What schools did Santina Spera attend?
Santina Spera holds Master Of Science - Ms, Pharmaceutical Sciences from Temple University.
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