Baris Consulting GmbH

Project Management | Business Development | Quality Management | GxP Support

About Us

Can Baris Can Baris (MA Pol. Sc.) has over 10 years of experience in Project Management and successfully completed more than 20 global Projects / Programs in his career so far. His core topics, which he drove as an external as well as an internal Project Manager, are Digitalization in Sales, Operations Improvements and M&A Execution. His expertise covers the design as well as the implementation phase until Go-Live (incl. handover to the business).

Sema Baris Sema Baris (Dr. sc. techn. ETH) has 20 years of experience as responsible person and Head QA in the pharmaceutical industry. She brings a wide range of expertise in GMP, GDP, GLP and GCP as well as CAPA management. As a qualified lead auditor, she has successfully carried out numerous audits in Switzerland and other European countries. Her close cooperation with health authorities has always yielded the desired results. Since 2017 Mrs. Baris is active as a consultant.

Halim Baris Halim Baris (Dr. sc. techn. ETH) with 30 years of experience in the industry has been involved in QM-Systems for Automotive since the first ISO/TS16949 in 1999 and looks now forward to support companies in the implementation of the new IATF16949 standard. Following his last function as Global QM Director in the semiconductor industry, Mr. Baris is now active as consultant.


« The time for action is now.
It’s never too late to do something.»

– Antoine de Saint-Exupéry



Baris Consulting, your partner with a proven track record in the pharmaceutical, manufacturing and insurance industry

Project Management

Leading (cross-functional) Projects and drive planning, stakeholder management, communication, dependencies & risk management. Preparing, moderating and post-editing workshops as well as supporting the creation of management reporting and presentations that serve as decision-making basis for e.g. the Executive Board.

Pharmaceutical Industry

Efficient, sustainable support in Audit Management & preparation / monitoring for Health Authorities Inspection, CAPA Management, Documentation, Risk Management, PQRs, Qualification / Validation, Deviation & Complaint Management. Interim QP/RP (FvP) according to Swissmedic Regulation (AMBV). Ensuring to fulfill all requirements according to GMP / GDP / GCP / GLP as interim / external Manager QS.

Quality Management

Preparations (GAP analysis, definition and follow-up of actions) to important audits according to ISO9001, IATF16949, ISO14001 and specific customer audits. Establishment of management systems and creation/improvement of documentation based on these standards. Optimizations in local and global QM-topics.


« Quality is not an act but a habit. »