Peter Riechel - Senior Associate

Recommended expert

Ingelheim am Rhein, Germany

Experience

Jul 2021 - Present

4 years 7 months

Germany

Senior Associate

Lachman Consultants

Apr 2019 - Present

6 years 10 months

Germany

Expert for Pharmaceutical Industry and Medical Devices

Clear Cube Consulting

Jul 2013 - Present

12 years 7 months

Germany

Interim Management, Consulting and Training

T3 Consulting

Provide interim management, consulting, and training services across quality management and compliance in the pharmaceutical and medical device industries.

Feb 2013 - May 2013

4 months

Stein, Switzerland

Head of QA Compliance Sterile Manufacturing

Novartis PharmOps

Apr 2012 - Dec 2012

9 months

Frankfurt, Germany

Group Leader Complaint Management

Sanofi Deutschland

Led two teams (16 direct reports) managing complaint handling at the Frankfurt Insulin site.

Apr 2010 - Mar 2012

2 years

Ingelheim am Rhein, Germany

Senior Manager Corporate Quality Assurance

Boehringer Ingelheim Corporate Center

Global process owner for complaints, leading a matrix organization for complaint officers worldwide and owning the global complaints database.
Developed and delivered worldwide trainings on complaints, recalls, and out-of-specification results.
Deputy global process owner for recalls, leading international crisis teams for recall decisions and follow-up actions.

Mar 2005 - Mar 2010

5 years 1 month

Ingelheim am Rhein, Germany

Head of Complaint Management Germany

Boehringer Ingelheim Pharma GmbH & Co KG

Led three groups (15 employees) within Process Quality Assurance/Quality Operations.
Served as responsible person for medical devices in Germany and the EU under Section 30 of the Medical Devices Act.
Participated in approximately 40 audits by FDA, Anvisa, KFDA, and other authorities.
Qualified co-auditor at BI Pharma GmbH & Co KG.

Oct 2000 - Feb 2005

4 years 5 months

Ingelheim am Rhein, Germany

Senior Manager Analytical Development, Animal Health

Boehringer Ingelheim Vetmedica GmbH

Led two laboratories: Analytical Development and New Analytical Technologies.
Coordinated external developments in the US and Europe during pre-formulation, formulation finding, and scale-up batches.
Audited raw material suppliers and contract manufacturers in Europe and the US.
Led CMC coordination for multiple international product development projects (chewable tablets, suspensions, injectables).

Oct 1998 - Sep 2000

2 years

Kiel, Germany

Analytical Development

Ferring Pharmaceuticals

Developed analytical methods for peptides and proteins using HPLC, CE, SEC, GC-MS, NMR, and other techniques.
Qualified and managed external contract laboratories across Europe.
Validated analytical methods according to ICH guidelines and performed stability studies.
Supported registration dossiers (CMC part of CTX and IND) and coordinated bioanalytical method development for preclinical studies.

Summary

Target-oriented. Quality Management professional with more than 25 years of experience in international operating companies.

Strong leadership skills.

Knowledge creates ways to form the future: A holistic view on the current situation is his trademark. Peter uses his experience in the field of life sciences in all areas and in all forms of industry.

As you can see, you can be a generalist and a specialist at the same time. And that is how his work is described in an accurate manner.

Skills

Interim Management
Cgmp And Gmp Compliance
Lead Auditor For Cgmp And Iso 13485
Analytical Development / Quality Control
Medical Devices / Drug Device Combination Products
Cross-functional Teams & International Project Management
Cmc Development Projects
Six Sigma / Business Process Excellence
Excellent Analytical, Conceptual, And Rhetorical Skills
Experience In Product Development And Production For Inhalation Technologies: Dry Powder Inhalers (Spiriva Handihaler, Advair Disc And Other Competitors), Meter Dose Inhalers, Soft Mist Inhaler (Respimat), Vaporizing Techniques
Experience In Product Development And Production For Prefilled Syringe Products
Experience In Product Development And Production For Sterile/aseptic Products Eu Gmp Annex 1
Experience In Product Development And Production For Solid Oral Dosage Forms Including Dissolution Methods And Bioequivalence