Head Qa, Bioeq Ag
Current
Feb 2024 - Present
Who is Peter Durrer? Overview
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Peter Durrer is listed as Head QA, Bioeq AG, Zug at Bioeq AG, based in Switzerland, Switzerland, Switzerland. AeroLeads shows a matched LinkedIn profile for Peter Durrer.
Peter Durrer previously worked as Head QA, Bioeq AG at Bioeq Ag and Head QA Systems at Bioeq Ag. Peter Durrer holds Doctor (Phd) In Natural Sciences (Diss. Eth No. 12357), Biochemistry from Eth Zürich.
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Bioeq AG
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Profile bio
About Peter Durrer
Demonstrated success directing cross-functional groups to streamline Quality Assurance/Control, Regulatory Affairs, IT, Pharmacovigilance, and GMP manufacturing operations that drove maximum profits. Solution-focused and change-driven leader leveraging sound experience developing and reviewing quality and regulatory metrics that control high risks within clinical and manufacturing plans. Thought leadership approach to build, train, and improve QA, RA, and PV teams in line with KPIs and state of the art GxP standards. Analytical thinking with solid record of delivering best-in-class solutions to deal within volatility, uncertainty, complexity, and ambiguity environment. Recognised as a GxP expert for ensuring quality of medicinal products while establishing new emerging systems.
Listed skills include Gute Klinische Praxis, Pharmaindustrie, Validation, Pharmaceutical Industry, and 22 others.
Current workplace
Peter Durrer's current company
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10 roles
Peter Durrer work experience
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Head Qa Systems
Apr 2023 - Feb 2024
Head Quality Assurance Systems & Compliance
Accountable of quality assurance, regulatory affairs and Pharmacovigilance within organisation. Since Nov 2019 Liaison Manager for SAKK Working Group for Cellular Therapies. Following are the key achievements:- Led over 20 good clinical and manufacturing practice (GCP and GMP) audits.- Ensured submission, execution, and termination of results information.
Oct 2021 - Apr 2023
Ceo Ad Interim & Head Quality Assurance, Regulatory Affairs & Pharmacovigilance
Sakk Swiss Group For Clinical Cancer Research
I manage development and execution of high-level business operations to meet company’s targets. In the absence of chief executive officer I control and monitor company's overall operations. Here are some key contributions:- Led continuous improvement of quality assurance and regulatory affairs department within organisation. - Enabled continuous evaluation.
Dec 2018 - Sep 2021
Head Quality Assurance & Regulatory Affairs And Member Of The Executive Board
I undertook full accountability of quality assurance and regulatory affairs within organisation. Following are the key achievements:- Implementation of phase I site selection audits by streamlining risk-based strategy.- Ensured submission, execution, and termination of results information on clinical trials under Swiss and EU laws with the development of.
Jan 2011 - Dec 2015
Head Quality Assurance And Gcp Compliance
I headed quality assurance procedures, comprising of documentation, training programmes, corrective/preventive actions, change control, deviation, and auditing. I identified and defined GCP and regulatory requirements for investigators and clinical research colleagues as an expert presenter.Here are few key accomplishments:- Planned and delivered.
Nov 2009 - Dec 2010
Senior Director Quality Affairs
I undertook full accountability of quality assurance and quality control within organization of the GMP vaccine manufacturing site in BernFollowing are the key achievements:- Managed quality assurance and control of the GMP vaccine production site in Berne consisting of 65 head counts.- Directed national and international inspections, including FDA.
Jul 2007 - Oct 2009
Director Quality Control Operations
Director of Quality Control unit at the vaccine manufacturing site Bern, consisting of QC Chemistry, QC Virology, QC Bacteriology, QC Monitoring and a small animal testing facility for QC release testing of vaccines. Laboratory met cGMP standards, which was verified by national and international routine inspections (FDA, WHO, Swissmedic etc.). In addition.
Jan 2005 - Jun 2007
Head Of Quality Control
Head of Quality Control unit consisting of QC Chemistry, Virology, Bacteriology and Monitoring and a small animal facility for specific QC release tests (in all 40 co-workers).QC release testing of all biological products manufactured at the site Bern (Vaccines and serological products). Laboratory was cGMP compliant and regular inspected by FDA.
Jan 2002 - Dec 2004
Head In-Process-Control
Head of laboratory Virology and Serology. Laboratory met cGMP quality management standards. The main scope was on product development, manufacturing control and monitoring.
Nov 1997 - Dec 2001
2 education records
Peter Durrer education
Doctor (Phd) In Natural Sciences (Diss. Eth No. 12357), Biochemistry
Eth Zürich
Diploma Study And Diploma Thesis In Natural Sciencis, Biochemistry
Eth Zürich
FAQ
Frequently asked questions about Peter Durrer
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What company does Peter Durrer work for?
Peter Durrer works for Bioeq AG.
What is Peter Durrer's role at Bioeq AG?
Peter Durrer is listed as Head QA, Bioeq AG, Zug at Bioeq AG.
Where is Peter Durrer based?
Peter Durrer is based in Switzerland, Switzerland, Switzerland while working with Bioeq AG.
What companies has Peter Durrer worked for?
Peter Durrer has worked for Bioeq Ag, Thermo Fisher Scientific, Sakk Swiss Group For Clinical Cancer Research, Crucell, and Berna Biotech Ltd.
How can I contact Peter Durrer?
You can use AeroLeads to view verified contact signals for Peter Durrer at Bioeq AG, including work email, phone, and LinkedIn data when available.
What schools did Peter Durrer attend?
Peter Durrer holds Doctor (Phd) In Natural Sciences (Diss. Eth No. 12357), Biochemistry from Eth Zürich.
What skills is Peter Durrer known for?
Peter Durrer is listed with skills including Gute Klinische Praxis, Pharmaindustrie, Validation, Pharmaceutical Industry, Glp, Gute Laborpraxis, Produktentwicklung, and Pharmacovigilance.
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