Recruitment Information

• Pharmaceutical R&D Manager

  
  Job Responsibilities

  • •Be responsible for the overall planning and technical route design of cephalosporin antibiotic R&D projects in the field of synthetic processes.
  • •Lead the process development, optimization, and commercialization of cephalosporin antibiotics.
  • •Manage the R&D team, coordinate resources, advance project progress, and ensure the achievement of R&D goals.
  • •Establish and maintain an R&D quality management system that complies with GMP and EU certification requirements.
  • •Participate in cross-departmental collaboration and provide technical support and solutions for production, quality, and other departments.
  • •Track domestic and international technological developments in the field of cephalosporin antibiotics and put forward innovative R&D suggestions.

  Qualifications

  • •Education: Master's degree or PhD required. Candidates with a background in medicinal chemistry, organic synthesis, pharmaceutics, or related fields will be preferred.
  • •Work Experience: At least 5 years of experience in cephalosporin antibiotic R&D. Candidates with end-to-end project development experience will be preferred.
  • •Professional Skills: (1) Familiar with the full process of cephalosporin antibiotic synthesis process development. (2) Proficient in organic synthesis techniques and analytical method validation. (3) Familiar with relevant regulatory requirements related to GMP, ICH, and EU certification. (4) Possess team management and cross-departmental collaboration capabilities.
  • •Candidates with working experience in the R&D department of a pharmaceutical enterprise will be preferred.
  • •Candidates familiar with project management methodologies and with practical application experience will be preferred.
  • •Good command of English in listening, speaking, reading, and writing. Candidates able to read foreign literature and technical materials will be preferred.
  • •Candidates with patents or published papers related to cephalosporin antibiotics will be preferred.

• Medical Affairs Manager

  
  Job Responsibilities

  1.Medical Evidence Management: Participate in the design of clinical trial protocols, data interpretation, and medical writing for products; assist in advancing post-marketing real-world studies and other medical affairs activities; collect and analyze clinical data, establish the medical evidence chain, and ensure standardized documentation and archiving.

  2.Medical Information Analysis: Track medical developments in the industry, guideline updates, and competitor activities; organize and analyze relevant information to provide data support for R&D and academic product promotion.

  3.Academic Promotion and Communication: Formulate academic promotion strategies and plans, organize various academic activities, build networks with key opinion leaders, conduct compliant academic communication, convey the scientific value of products, and address clinical questions.

  4.Medical Support and Consultation: Provide medical support for internal and external stakeholders, offer medical insights on product development and marketing strategies, and handle medical inquiries from clinical and market sides.

  5.Innovative Product Evaluation: Participate in innovative pipeline planning and project evaluation, and provide medical support for the introduction of innovative projects.

  6.Cross-functional Collaboration: Work closely with BD, R&D, marketing, sales, and other departments to advance related work.

  Qualifications

  1.Master’s degree or above in a pharmaceutical or medical-related field.

  2.Candidates with relevant work experience in medical affairs within the pharmaceutical industry will be preferred.

  3.Strong English skills in listening, speaking, reading, and writing.

  4.Good communication skills, medical writing ability, and data analysis skills.

• Pharmaceutical Quality Manager

  
  Job Responsibilities

  1.Responsible for the following work related to export products: 1. Design, establish, and manage the GMP documentation system involved; review quality standards, process procedures, and change control documents to ensure compliance.

  2.Make decisions on the use of materials and intermediates; review plans for recalls, returns, and the handling of non-conforming products; organize deviation investigations and corrective and preventive actions.

  3. Collaborate with the supply department in auditing key material suppliers, evaluate their quality assurance capabilities, and supervise workshop quality control points and material management.

  4.Organize validation activities, identify quality risks in the production process, and conduct product quality review analysis and trend evaluation of monitoring data.

  5.Develop stability study plans, review training plans, organize quality analysis meetings, and communicate and coordinate with drug regulatory authorities to complete report submission and temporary tasks.

  Qualifications

  1.Bachelor’s degree or above in medicine, pharmacy, or a related field, with at least 5 years of work experience; familiar with domestic and international laws, regulations, and standards.

  2.Excellent communication, presentation, document writing, and data analysis skills, with the ability to handle various challenges independently.

  3. Strong team management and coordination skills.

  4.Has received various professional trainings related to injectable product manufacturing.

• API Workshop Director

  
  Job Responsibilities

  1.Be responsible for the daily production management of the company’s active pharmaceutical ingredient workshop.

  2.In accordance with GMP management requirements, supervise the production process, quality tracking, and equipment maintenance of the workshop; organize and reasonably arrange workshop personnel; and complete the production tasks assigned by the company with guaranteed quality and quantity.

  3.In accordance with GMP standards and requirements, organize training for workshop personnel on operating procedures, safety, environmental protection, and other related knowledge, so as to improve staff competence and enhance production efficiency.

  4.Complete other tasks assigned by the company.

  Qualifications

  1.College degree or above in chemical engineering, fine chemicals, pharmaceutical engineering, or a related field, with at least 5 years of experience in API process technology or production management.

  2.Familiar with the facilities and equipment of an API workshop, and capable of managing the construction of workshop production lines.

  3.Familiar with GMP and knowledgeable about relevant laws, regulations, and policies.

  4.Possess a strong sense of responsibility and dedication, as well as strong communication, coordination, organization, and planning abilities, with the ability to work under pressure.