Careers
Working at Synermore

With the company's sustained and rapid development, Synermore has provided many challenging opportunities for the experienced professionals in various fields. What we look forward to is the involvement of scientific and commercial professionals who are innovative, energetic and aggressive in the innovation and development of monoclonal antibody drugs. Synermore will provide every employee with good salary, welfare benefits and training opportunities for promotion. We warmly welcome you to join us. We believe Synermore will become a place where you can realize your dream.

Welfares: Social Security Provident Fund, holiday gifts, wedding gifts, birthday gifts, birth gifts, annual health examination, commercial accident insurance & supplementary medical insurance, annual dinner, departmental activities, corporate activities, external training, collective household registration, etc.             

Resume delivery mailboxymsun@synermore.com

Tel:(860512-87658266

                

Currently Job Opening at
Suzhou
Cell Culture Senior Engineer
Job description

1. Operation of a large-scale disposable bioreactor and culture medium according to the technological requirements.

2. Drafting and revising SOP, batch records, URS, verification files, etc.

3. Conduct processing, cleaning and method validation according to process procedures in line with GMP production requirements.

4. Cell culture condition optimization, amplification and stereotype, transfer work.

5. Proficiency in the production of relevant testing equipment and auxiliary equipment, and complete the record.

6. Other tasks arranged by the leader.


Requirements

1. Bachelor degree or above in Biology or Pharmaceutical, 3 years or more experience in bio-pharmaceutical industry.

2. Experience in large-scale production or pilot-scale production of cell culture; Facility installation, commissioning, FAT, SAT, TQ, OQ experience is preferred;

3. Good sense of GMP and be able to adapt to clean area environment;

4. Proficiency in using disposable bioreactor (SUB) or stainless steel bioreactor, liquid dispensing, harvesting system and related testing equipment.

5. Proficient in reading literatures, and listening and speaking abilities in English.

6. Proactive, responsible, honest, hardworking, good communication and good sense of teamwork.


Location: Building 5 of Sang Tian Island Bio Industry Park, 218 Sangtian Street, Suzhou Industrial Park, Jiangsu.

Please send your resume to 51job or Liepin or send it to ymsun@synermore.com for details.


Formulation Senior Engineer
Job description

1. Perform monoclonal antibody injections production according to formulation SOP; ensure that production tasks are completed in accordance with the plan and GMP requirements;

2. Responsible for the drafting and implementation of the verification work plan for the simulation filling.

3. Responsible for drafting related technical documents, including batch production records, process regulations, operation procedures, etc.

4. Responsible for the equipment management and daily maintenance of the preparation workshop, cooperate with others to deal with equipment failure problems to ensure the normal production;

5. Participate in deviation survey and write deviation survey report.




Requirements

1.Bachelor degree or above in pharmaceutical engineering, pharmaceutics and other related majors; 3 years or more relevant working experience in bio-pharmaceutical industry

2. Master injection production process, familiar with aseptic preparation GMP knowledge;

3. Proficient in literature reading, and listening and speaking abilities in English.

4. Proactive, responsible, honest, hardworking, good communication and good sense of teamwork.


Location: Building 5 of Sang Tian Island Bio Industry Park, 218 Sangtian Street, Suzhou Industrial Park, Jiangsu.

Please send your resume to 51job or Liepin or send it to ymsun@synermore.com for details.

Microbiological Analysis Senior Engineer
Job description


1. Responsible for drafting the management and standard operating procedures of various automatic control systems (such as ERP/SCADA/EMS/MES/LIMS) to ensure the effective operation of each software system;

2. Responsible for daily operation maintenance and data storage management of the automation control system (such as ERP/SCADA/EMS/MES/LIMS) installed by the company.

3. Responsible for coordinating the establishment of alarm limit setting and alarm information notification management procedures for various departments to ensure the effective operation of quality-related dynamic monitoring system.

4. Responsible for organizing the scanning, auditing and archiving of batch production records and inspection records.

5. Responsible for privilege settings of all the company's storage, production and testing related computer and operating system to ensure the integrity of electronic data, non-modification and traceability;

6. Draft or review verification schemes and reports for each software system, organize and implement them, record all abnormal situations, report to the supervisor in time, and ensure that all deviations and revisions of documents are effectively handled and approved.

7. Cooperate with regular internal audit and quality review activities.

8. Complete other tasks arranged by the leader.












Requirements

1. Bachelor degree or above in Pharmacy or other related fields, 3 years or more QC test related work experience in bio-pharmaceutical industry;

2. Skilled in aseptic testing, microbial limit testing, endotoxin testing, environmental testing, etc.

3. Skilled in using dust particle counter, plankton sampler, compressed air detector and other analytical equipment.

4. Proficient in literature reading, and listening and speaking abilities in English.

5. Proactive, responsible, honest, hardworking, good communication and good sense of teamwork.


Location: Building 5 of Sang Tian Island Bio Industry Park, 218 Sangtian Street, Suzhou Industrial Park, Jiangsu.

Please send your resume to 51job or Liepin or send it to ymsun@synermore.com for details.


Cell Analysis Senior Engineer
Job description

1. Drafting validation scheme, carrying out validation experiment and writing validation report according to the guiding principle of methodological validation.

2. Analysis and inspection of intermediate sample, finished product and stable sample, such as sterility, microbial limit, endotoxin, raw and auxiliary materials, package materials, pharmaceutical water-related microbial testing and clean area environmental testing.

3. Drafting and revising the inspection methods, standard operating procedures, inspection records and other documents.

4. Drafting and formulating the quality standards and verification rules of microbial testing instruments, and mastering the operation methods of each testing item.

5. Laboratory deviation (OOS, OOT) survey, writing deviation survey report.



Requirements


1. Bachelor degree or above in Pharmacy or other related fields, 3 years or more QC test related work experience in bio-pharmaceutical industry;

2. Skilled, in line with industry standard cell culture, ELISA, QPCR, CE and other skills;

3. Be able to skillfully use enzyme labelling instrument, fluorescence quantitative PCR instrument, capillary electrophoresis instrument and other analytical equipment.

4. Proficient in literature reading, and listening and speaking abilities in English.

5. Proactive, responsible, honest, hardworking, good communication and good sense of teamwork.


Location: Building 5 of Sang Tian Island Bio Industry Park, 218 Sangtian Street, Suzhou Industrial Park, Jiangsu.

Please send your resume to 51job or Liepin or send it to ymsun@synermore.com for details.