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CQA LEAD BENELUX
見る: 145
更新日: 16-11-2025
カテゴリー: その他の
業界: Chemical Manufacturing Biotechnology Research Pharmaceutical Manufacturing
レベル: Associate
ジョブタイプ: Full-time
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仕事内容
Functie- Responsible Person/Responsible Pharmacist:
– Act as Qualified Person (QP) as per ”preparation/MIA license” including final responsibility for final product certification, Annual Product Review, QMS in line with GMP etc…
- Responsible for QMS implementation:
– Develop and maintain Quality mindset in BDCE Operations
– Ensure that operational processes with related procedures and procedures for release are in place and comply with the applicable requirements and cGDP
– Ensure process and procedures are in place and in compliance with European, Local and Corporate requirements,
- Responsible for CQA BDCE operational activities:
– Be the local contact for Quality Audits and Supplier Quality
- Quality Support to local business initiatives in collaboration with Quality Operations
- Must possess a Master’s degree in Sciences, preferably in Pharmaceutical Sciences (or in (Veterinary) Medicine, Chemistry, Biology, Biomedical) to be in line with the local regulations for QP/RP
- Demonstrated ability to develop, apply and to operate within Company policies and procedures within Quality and Compliance area.
- Good verbal, written and presentation skills in English, to deal effectively with all levels of management.
- Team oriented worker with excellent interpersonal skills.
- Demonstrated ability to switch priorities and manage more than one project at the time. Ability to plan and conduct in projects within a multi-disciplinary environment, inquisitive, science technology oriented individual but practical.
- Demonstrated ability to influence, collaborate and communicate directly and to lead cross functional and cross regional teams.
- Strong negotiating skills for interfacing with Health Authorities and market business functions.
- Demonstrated ability to effectively communicate ideas, lead and persuade others to accomplish challenging goals and objectives
- 3-5 years of progressive managerial experience within the quality function of the pharmaceutical health care industry or with regulatory agencies
- Very good knowledge and experience in pharmaceutical health care operations, quality control, distribution and International regulations are essential.
- Proficient in cGMPs, GDPs and regulations promulgated by the FDA, EMA or equivalent regulatory Agencies; ISO 9000 regulations; and requirements for pharmaceutical products distribution.
- French and English language skills
Our client is a leader in medical innovations that are revolutionizing healthcare. If you too would like to contribute to the improvement of healthcare for patients, this is the place to be! We are recruiting a CQA LEAD BENELUX to join their team.
Aanbod
We offer you the chance to take on a managerial role in a leading company in its field. A long term contract and a very attractive salary, with very interesting extra-legal benefits.
Over ons
Talentus HR experts will put you in touch with your future employer. These passionate specialists work mainly for Belgian SMEs. Their mission is to select the best talents and to find you a tailor-made job.
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締切: 31-12-2025
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