Peter Schrijver Email & Phone Number

Panningen, LI, NL

Dordrecht, Provincie Zuid-Holland, Nederland

Adryan was founded in 2012 in Dordrecht. The founders, who are also responsiblefor the daily running of Adryan Consultants, have more than 20 years’ experience within the Beneluxas a consultancy and service provider in the pharmaceutical industry.Adryan Consultants has fixed staff employees and freelancers who are connected in the AdryanConsultants.

Friesoythe, Niedersachsen Germany

Interim Management position and expectations defined as a project, including milestones- Interim Manager AQC, leading a team of 16 analysts, running daily business, continuing running projects and starting planned new projects, Change Control, Deviation Management, Inspection programs etc.- Identify and hire successor for the position AQC Manager: hire for.

Bilthoven, Provincie Utrecht, Nederland

Assignment:- Member of the team that is responsible for the qualification of the restructured production facility intended to be used for the commercial production of Polio vaccins- Member of Serialisation project team

Burgwedel, Lower Saxony, Germany

Assignment:Member of the team that is resposible for the Performance Qualification of the newly build production facility (clean rooms class D to A), intended to be used for the commercial production of the Ebola vaccine.

Haarlem

• Assignment for MSD Haarlem:
• My responsibilities and tasks: In the role of Pharmaceutical Specialist for the 3 departments Vaccines packaging, Blister and Specialties packaging: o Deviation management, investigation and CAPA o Customer complaint.

Curaçao

Offering GxP compliance and Quality Assurance expertise.First assignment for Rescop: Smith & Nephew, CuraçaoDeviation/CAPA investigation expertTeam Lead Rescop team Curacao (team of 8 SME's)Work stream lead Deviation/CAPA remediation.(leading 15 (Sr) investigators)

Geleen

• Basic Pharma Manufacturing is a small but fast growing company for generic prescription and OTC products, specialised in crèmes, ointments, nasal spray products and (sterile) IMPs. Production is executed in cleanrooms.
• MT Member
• Leading the Quality Assurance department
• Guide and control the structure, improvements and maintenance of the pharmaceutical QMS, quality manual and GMP within the organisation
• Review and authorisation of Master QA documents
• Change Control, CAPAs, deviations and complaints

Boxmeer

• MSD Animal Health is the 2nd largest company (worldwide) for medicines, vaccines and drug administration devices for veterinary use, licensed in approx. 140 countries. My position as Document Management Officer was in.
• Support the GRA department by identifying and improving business processes necessary to obtain and maintain market authorizations, while improving efficiency and minimizing time to market.
• Group leader to recruit, supervise, and coach the document management team, consisting of 2 employees in Boxmeer, 1 in Schwabenheim, Germany, and 1 in Anger, France.
• Representative for MSD AH in the IFAH-Europe, a Veterinary Industry representation group in Brussels aimed at aligning industry needs with governmental requirements. As such, I also represented IFAH-Europe in meetings.
• Supervise and verify the quality of the electronic presentation of European dossiers based on the EMA guideline on e-submissions for veterinary medicines.
• Administration of supporting IT-systems and applications, electronic archives, shared drives, SharePoints, Document management systems and dossier compiling tools (Lorenz Docubridge, eCTD Office)

Venlo

• DSM Pharma Chemicals Venlo is mainly focussed on the production of Active substances and precursors for the Pharmaceutical Industry. As one of the Quality Assurance Officers at the Venlo site, I was responsible for the.
• QA Manual: Administration of the (quality) management systems (including ISO 9001, 14001 and DSM internal SHE requirements) and documentation (Policies, SOPs and instructions)
• Perform and report Management quality reviews (ISO 9001)
• Draft PQRs (product quality reviews)
• Draft and maintain the Site Master Validation Plan (SMVP)
• Support in drafting quality contracts with customers and suppliers.