Welcome to join us
We have different professional backgrounds and fulfill the same commitment in different jobs to provide professional product solutions to our customers.
As a member of INNOPAC, we are actively focusing on the innovation of new high-end pharmaceutical and medical device packaging materials, fulfilling our social responsibility and achieving corporate development, while making the relationship between the enterprise, society, doctors and patients more harmonious, and making our employees' work happier and life better. What you will get at Sinopac is not just a job, but a platform to explore more potential and a career full of challenges and opportunities.
We welcome you to apply for a job at INNOPAC and create and achieve more goals together with us.
Interview consultation telephone
86-021-57898778
Resume Submission Email
hr@innopac.com
- System QA Engineer
Recruitment company: Shanghai Bravo Technology Co.,Ltd.
Recruitment number: 1 person
Working years: 2 years
Educational requirement: Bachelor degree (or above).
Professional requirements: Medicine, pharmacy, chemistry, polymer materials and related majors
Job duties:
1. Responsible for the operation and supervision of the elements of the quality assurance system, to ensure the effective implementation of the company's quality management system.
2. Responsible for the system internal audit, management review work, including plan development, the first and last meeting organization, process participation, results collection feedback, follow-up implementation of follow-up measures.
3. Pay attention to customer needs and customer satisfaction surveys, and assist in customer site audits.
4. Participate in the construction and continuous improvement of the company's quality management system, and assume the responsibility of promoting the training of system documents.
5. To identify supplier qualifications, participate in on-site audits and daily reviews of suppliers, and perform supplier management functions.
6. Responsible for changes related to product quality, responsible for the assessment of the implementation effect of the whole process, such as drafting of change documents, training, tracking and implementation of the change process, regular review and archiving of changes.
7. Responsible for all measurement work: measurement and monitoring device control procedure document development and maintenance, measurement work annual/monthly plan, update measurement ledger, measurement work implementation, period verification, etc..
8. Responsible for the collection and analysis of annual quality review data, drafting of annual review documents for each product, and meeting with relevant departments to review annual product quality reports.
9. Responsible for the development, implementation and tracking of CAPA, and evaluation of the implementation effect.
Job requirements:
1. Bachelor degree or above.
2. Medicine, pharmacy, chemistry, polymer materials and related majors.
3. At least 2 years of experience in quality management.
4. Strong interpersonal communication, coordination, organizational skills and high team spirit, strong sense of responsibility and strong principles.
5. With proficient office automation skills, excellent English proficiency, able to read and write English proficiently.
6. Familiar with ISO13485\ISO9001\ medical device or drug GMP and other quality management system knowledge, with sterile drugs or sterile medical device system operation and maintenance management experience is preferred.
- Validation Engineer
Recruitment company: Shanghai Bravo Technology Co.,Ltd.
Recruitment number: 1 person
Working years: 2 years
Educational requirement: Bachelor degree (or above).
Professional requirements: Medicine, pharmacy, chemistry, polymer materials and related majors
Job duties:
1. Responsible for the preparation of validation master plan, non-conventional project validation plan preparation and validation work promotion.
2. Responsible for drafting, revising relevant validation management documents, not limited to validation of equipment and facilities, utility systems, processes, cleaning, etc..
3. Responsible for the organization, coordination and implementation of the validation work.
4. Responsible for reviewing URS/FAT/SAT validation and confirmation programs/reports, etc., and responsible for the archiving of documents after the validation activities.
5. Responsible for the investigation and handling of deviations and changes that occur during the implementation of validation and confirmation, and participate in risk assessment.
6. Responsible for collecting and organizing the latest validation knowledge and related regulations, and responsible for internal training of validation management knowledge.
7. Responsible for coordinating third-party validation companies to carry out validation work.
8. Participate in the validation work in the product design and development process of the R&D department.
9. Participate in the validation and confirmation work of company review, annual quality review, change management, deviation management and other processes.
Job requirements:
1. Bachelor degree or above.
2. Medicine, pharmacy, chemistry, polymer materials and related majors.
3. At least 2 years of validation work experience.
4. Strong interpersonal communication, coordination, organizational skills and high team spirit, strong sense of responsibility and strong principles.
5. With proficient office automation skills, excellent English skills, able to read and write English proficiently.
6. Knowledge of ICH, GXP regulations, ISO and other regulatory knowledge of pharmaceutical industry or medical device industry, experience in validation of sterile drug or sterile medical device system is preferred.
- QC
Recruitment company: Shanghai Bravo Technology Co.,Ltd.
Recruitment number: 1 person
Working years: 2 years
Education requirement: Bachelor degree
Job duties:
1. Responsible for raw materials, intermediate products, finished products inspection and issuing inspection reports.
2. Responsible for medical and pharmaceutical package clean environment monitoring and analysis.
3. Responsible for the development of inspection quality control standards.
4. Responsible for the establishment of quality control documents SOP update.
5. Responsible for the establishment of test methods.
6. Responsible for the development of CAPA for the investigation and processing of deviation of test data over trend.
7. Responsible for the measurement and calibration of testing instruments and equipment, the establishment of equipment files, equipment maintenance and management.
8. Responsible for the verification of the stability and compatibility of pharmaceutical packaging materials.
9. Process customer feedback and develop corrective and preventive measures.
10. To complete other tasks arranged by the leadership.
Job requirements:
1. More than 1 year of pharmaceutical / medical devices / medical / pharmaceutical packaging materials / polymer / materials and other laboratory analysis and testing capabilities.
2. With a certain degree of communication and coordination skills.
3. Good data analysis and interpretation ability.
4. Welcome fresh graduates of excellent pharmaceutical-related majors to join us.
- Material Engineer
Recruitment company: Shanghai Bravo Technology Co.,Ltd.
Recruitment number: 1 person
Working years: 2 years
Education requirement: Bachelor degree
Job duties:
1. According to the work procedures to do a good job of horizontal contact with relevant departments
2. Propose the development direction of new products and project application for approval
3. Propose new product design plan and trial production plan, submit for approval and then organize the implementation
4. Access to new materials, drawing on new formulas and new processes, research and development of new formulas and new processes suitable for the actual situation of our company
5. New technologies, new processes and product formulations of confidential work
6. To assist in technical negotiations and external technical exchanges
7. Representation to direct superiors on a monthly basis
8. Cooperate with superiors to do the relevant research and development work, and do a good job of tracking the production site of new products
9. Do a good job in the summary analysis of various technical documents archiving work
Job requirements:
1. Bachelor degree or above, majoring in material science and engineering, chemical analysis and synthesis or chemical related majors
2. English level 4 or above, with basic English listening and reading skills
3. With a basic knowledge of polymer materials production and processing, or experience in chemical and chemical synthesis, familiar with the process flow of each process.
4. Familiar with the basic knowledge of material properties and processing related professions, or the basic knowledge of chemical and chemical processes, with basic knowledge of various computer software operations.
5. Have good learning ability and in-depth research ability, can consult relevant books and literature well, good at learning, thinking and doing.
6. Have a sense of innovation, on the basis of mastering the laws of innovation, methods and professional knowledge, dare to act, be good at acting and make a difference;
7. Have the ability to analyze and summarize, be familiar with the routine application of computers; have the ability to communicate effectively. Have certain ability of personnel management.
8. Good mental and physical qualities, adapt to various difficulties and challenges, adjust in time and adapt well to the work environment.
- Design Control Engineer
Recruitment company: Shanghai Bravo Technology Co.,Ltd.
Recruitment number: 1 person
Work experience: More than 2 years
Education requirement: Bachelor degree
Job duties:
1. Project implementation process quality assurance and supervision, according to the actual project development in the stage, supervise the project team to arrange design review, verification and confirmation, participate in design review, verification and confirmation. Ensure that each stage of the new product is in the system control support
2. Collect and feedback the problems (or non-conformities) and improvement suggestions in the product development process, promote the cause analysis and corrective prevention by the relevant responsible persons, and follow up and verify the corrective and preventive measures
3. To ensure that the R & D project team strictly comply with the product design and development process, and meet the quality requirements of the product development phase
Job requirements.
1. Familiar with ISO15378, ISO13485, GMP and other related quality system regulations
2. Familiar with medical device industry standards
3. Strong sense of responsibility, good at learning, strong communication skills
4. Proficient in English is preferred
- Strategic Planning Specialist
Recruitment company: Shanghai Bravo Technology Co.,Ltd.
Recruitment number: 1 person
Working years：1 year or more
Educational requirements: Bachelor degree (or above).
Professional requirements: Medicine, pharmacy, chemistry, polymer materials and related majors
Job duties:
1. Assist department leaders and the board of directors to analyze macroeconomic situation, industry policies, laws and regulations, and study relevant industry reports.
2. Assist department leaders to prepare short, medium and long-term development goals and strategic deployment plans for the company, draft strategic deployment plans, and participate in regular meetings to diagnose and amend the company's strategy to ensure that the company adapts to the changing environment.
3. Conduct feasibility studies for new projects and coordinate with relevant departments for initial project implementation and operation.
4. Participate in new areas, new projects and other preliminary business development work, business negotiations and specific project follow-up.
5. Cooperate with R&D, production, quality, marketing and other departments, responsible for the implementation and execution of new projects, immediate coordination of communication and resource allocation among departments to ensure the steady implementation of new projects and transfer to regular product business
6. Participate in the company's investment and financing business, output relevant project plans
Job requirements.
1. Bachelor degree or above in science and technology, master degree or higher is preferred.
2. Strong interpersonal communication, coordination, organizational skills and high team spirit, strong sense of responsibility and strong principles.
3. With proficient office automation skills, excellent English proficiency, and the ability to read and write English proficiently.
