Manager Supply Chain Quality - Temporary - 3 months (with a chance of extension) - fulltime

Location: Netherlands

SIRE® is the market leader in Life Sciences recruitment. We believe the recruitment market needs to gear up in technology and continuous innovation. We like technology, in a Life Sciences market driven on science, we couldn’t stay behind; we drive Recruitment Science. Investing a majority of our turnover in technology enables us to use unique Resource Technologies. By using highly advanced algorithms, we enable our team of Resource & Data Strategists© to maintain the most advanced, detailed and complete Life Sciences network in Europe. This big data enables us to work Reverse Recruitment©: we first analyze the market in-depth before we go out to the market. Because we analyze the whole market, we can compare facts and data. This enables us to do Facts & Big Data Recruitment©, making sure we, or better yet, you find the right career!Our client is a professional Pharmaceutical and Biotechnology organisation, based in Noord-Holland Netherlands.

The Company

The company is an international, pharmaceutical company that focuses on research and development, production and marketing of medicines. They have the ambition to be a sustainable partner in healthcare worldwide, focused on the needs of patients.

Role Description

You will be responsible for the GMP / GDP activities for the global distribution of the products from a quality perspective. Furthermore, you are offering support towards the QA team as well by taking management responsibilities as development of the training program. It's a challenging role where you are the contact person for the logistics partner when there are certain issues with the company's products. Besides this, you will take over management responsibilities and tasks whenever the manager and director are not available.

Responsibilities

You will be responsible for all GMP / GDP related activities and for overseeing the legal and regulatory compliance regarding Global Supply Chain Quality for the company.
- Implementing and coordinating the Quality Systems and Supply Chain Quality
- Legal and Regulatory compliance and Risk Management
- Managing projects (responsible for the delivery of complex cross functional / regional projects, from setup through execution and reporting to closure)
- Actively participates in and contributes to global business process improvement activities, representing the regional business view

Requirements

- University degree, preferably in Biosciences (Pharmacy, Biotechnology)
- Additional qualification as an industrial pharmacist or GDP Responsible Person is preferred
- 5+ years of experience in the Pharmaceutical industry in a similar position
- Experience in process improvement, compliance and auditing activities is required
- Experience with and knowledge of Quality Systems (GMP, GDP) is a must

Other information

- Has an analytical and pragmatic problem solving approach
- Strong planning, project, process, time, budget and people management abilities
- Excellent judgement with an eye for detail
- Strong communication, negotiation and networking capabilities
- Team player and to be able to work with several disciplines in a multicultural setting
- Is able to lead and organize others without having direct authority
- Is able to multi-task, prioritize and performs well under pressure
- Result driven
- Has a strong understanding of organizational and inter-cultural sensitivities and is able to apply this knowledge to day-to-day practices
- Fluent in verbal and written English (additional languages are preferred)

Are you interested and do want to apply for this role, please fill out your application via the apply button below and contact Bram Reulen.