Since 2015, Stan Szpindor has been working in Idera Pharmaceuticals based 3485, 3485. Stan Szpindor is an experienced Senior Director, Quality Assurance with over 21 years of work experience. According to Stan's CV and work profile, Stan Szpindor has worked at more than seven places with numerous backgrounds and gained various skills. Stan attended school at the Temple University from 1995 to 2000. Stan Szpindor has the following certificates: Sqa Registered Qa Professional - Gcp. Souderton, Pennsylvania is the place where this professional presently lives. You can search for this expert's phone and email. We can also provide you detailed contact information upon request.
Name variants:
Stanislas Szpindor,
Stanley Szpindor
Last updated Jun 09, 2024
Contact Information
Last Update
Jul 4, 2022
Email
ss**@iderapharma.com, ss**@comcast.net
Location
Souderton, PA
Company
Workplace
Colleagues
Work History
Senior Director, Quality Assurance
505 Eagleview Blvd, Exton, PA 19341
Idera Pharmaceuticals is a clinical stage biotechnology company with expertise in discovering, developing and commercializing novel nucleic acid therapeutics to treat patients with serious a...
from 2015
Head, R and D Qa and Compliance - Internal Process and Technology Compliance Center of Excellence
Developed quality strategy and led COE team focused on internal process compliance, R&D technology compliance/computer system validation, R&D due diligence assessments, and quality work stre...
2014 — 2015
Director, R and D Quality Assurance
Led R&D quality and compliance programs with focus on GCP, GLP, GPvP, IT Compliance / Computer System Validation, Due Diligence, and Regulatory Agency Inspection readiness. Hosted global Reg...
2006 — 2014
Practice Leader
201 south Biscayne Boulevard Way, Miami, FL 33131
Managed the GCP Practice and team of consultants providing audits, assessments, training, and inspection readiness activities to global biotech, pharma, and other healthcare clients.
2004 — 2006
Director, Quality Assurance
Pennsylvania
Established the Quality Assurance function and Quality Management System for the start-up biopharmaceutical company which spanned GCP, GLP, GMP, and Computer System Validation. Coordinated i...
2000 — 2004
Director, Quality Services
201 east 4Th St, Cincinnati, OH 45202
Established and managed a subset of the global QA function that was exclusively focused on start-up biotech and medical device firms to support the implementation of R&D quality systems.
1999 — 2000
Director and Assoc Director and Manager and Senior Auditor and Auditor, Clinical Quality Assurance
Quality management positions of increasing responsibility to ensure the delivery of GCP auditing services and compliance with internal quality system requirements.
1994 — 1999
Education
1995 — 2000
1987 — 1991
1983 — 1987
Occupations
Executive
Senior Director
IT Professional
Software Tester
Scientist
Biotechnology Professional
Senior Manager
Operations Manager
Computer Specialist
Biologist
Biological Scientist
Skills
Fda
Pharmaceutical Industry
Gcp
Clinical Trials
Biotechnology
Clinical Development
Quality Assurance
Computer System Validation
Regulatory Affairs
Glp
Gxp
Quality System
Regulatory Submissions
21 Cfr Part 11
Cro
Validation
Ind
Sop
R&D
Biopharmaceuticals
Clinical Research
Drug Development
Ctms
Oncology
Pharmacovigilance
Regulatory Requirements
Change Control
Capa
Vaccines
V&V
Technology Transfer
Gmp
Ich Gcp
Edc
Due Diligence
Medical Affairs
Mhra