Education:Doctor
Release date:
Salary:Negotiable
Work experience :Unlimited experience
City:Guangdong Province
Categories: Biopharmaceutical technology, Biotechnology
First-level areas:Biotechnology
First-level areas:Biopharmaceutical technology
Source:Social Recruitment
Job description :
Job Responsibilities.
As the main person in charge of the analysis department, leading the company’s project and analysis platform team, all tasks include strategy, technical solutions, and personnel management.
2. Coordinate and arrange work within the technical platform management coordination group, guide team members to carry out platform related method development/optimization, confirmation, and transfer related work. Identify and resolve platform technical issues and bottlenecks.
3. Project management coordinates the analysis and testing work of one or more projects, and regularly organizes, analyzes, and reports data.
4. The comprehensive affairs management of the overall platform is responsible for guiding the affairs specialist to manage and maintain the safety and hygiene of the technical platform, regular calibration and maintenance of instruments and equipment, compliance and timeliness of experimental records, sample reception and distribution, reagents and reagents, technical documents, etc.
5. Team training and assessment assess the performance of team members, and be responsible for talent development and training plans, consolidating the team, and maintaining team stability.
6. Writing application materials and reports for the responsible project, including application materials and various research reports.
7. Complete other work tasks temporarily assigned by superiors.
Job requirements.
1. Doctoral degree, with over 3 years of experience in biopharmaceuticals; At least 1 year of team management experience;
2. Proficient in theoretical knowledge related to chromatographic analysis, familiar with the use and maintenance of analytical instruments such as HPLC/UPLC;
3. Familiarize and master the development/optimization ideas of analytical methods, the process of method confirmation and transfer;
4. Familiarize oneself with relevant regulations and guidelines for the pharmaceutical industry such as pharmacopoeias and GMP in various countries;
5. Familiar with the basic processes of upstream and downstream processes, able to effectively support process development;
6. Possess excellent problem-solving skills, communication abilities, and overall coordination skills;
7. Possess good ability to work under pressure.
Please send your CV or resume as an attachment to the following email address:
mailto: rbhr@hrcenter.co.uk
With the subject line formatted as: ‘Name + Position + Company Name + Location’.