
Product Channel Manager
Job requisitis
I. Magister gradu seu supra;
II. Plus quam III annos experientia in investigationis Reagents, Sales vel ipsum administratione;
III. Bonum organization, planning, control et coordinatio artes, bonum interpersonalem artes, fortis communicationis et procuratio artes;
IV. Nota cum current situ vitae scientia products domi et foris, intelligere principalis customers et distributors demanda notitia;
V. fortis sensus officii, potest resistere intensa opus pressura et iter, cum Collaboratio maximi momenti spiritus;
Job officia
I. Et responsible foro progressionem et promotionem de comitatu scriptor reagentia et alia products in agro vitae scientiarum;
II. Responsible pro National Agentia de pertinet products, forum channel development, etc.;
III. Specializing in notam familiis et agentibus, dealers mos progressionem et promotionem;
IV. Ut develop et amplio comitatu scriptor altiore uber venalicium belli, exsequendam progressio, ut adiuvaret in perficiendis productum venalicium planning in progressionem pertinet organizations et instituta, Liamaon, coordinationem, etc.;
V. adiuvaret in foro investigationis, coordinatio de comitatu scriptor novum uber progressionem et originale productum emendationem;
VI. Alia opus assignata superior;
Opus Location: Shanghai
Placere submittere CV ad:Wangxx@hillgengener.com
I. Magister gradu seu supra;
II. Plus quam III annos experientia in investigationis Reagents, Sales vel ipsum administratione;
III. Bonum organization, planning, control et coordinatio artes, bonum interpersonalem artes, fortis communicationis et procuratio artes;
IV. Nota cum current situ vitae scientia products domi et foris, intelligere principalis customers et distributors demanda notitia;
V. fortis sensus officii, potest resistere intensa opus pressura et iter, cum Collaboratio maximi momenti spiritus;
Job officia
I. Et responsible foro progressionem et promotionem de comitatu scriptor reagentia et alia products in agro vitae scientiarum;
II. Responsible pro National Agentia de pertinet products, forum channel development, etc.;
III. Specializing in notam familiis et agentibus, dealers mos progressionem et promotionem;
IV. Ut develop et amplio comitatu scriptor altiore uber venalicium belli, exsequendam progressio, ut adiuvaret in perficiendis productum venalicium planning in progressionem pertinet organizations et instituta, Liamaon, coordinationem, etc.;
V. adiuvaret in foro investigationis, coordinatio de comitatu scriptor novum uber progressionem et originale productum emendationem;
VI. Alia opus assignata superior;
Opus Location: Shanghai
Placere submittere CV ad:Wangxx@hillgengener.com
Volume Project Manager
Job officia
I. Et responsible pro administratione de orci iudicii projects, portare de comprehensive qualitas imperium et progressus administratione, et ut orci iudicii projects sunt ferri in stricte secundum GCP, Sop, Tentatione protocols et pertinet leges et iudicii protocols et pertineret leges et iudicii;
II. Formulat Management consilia in linea cum project requisitis, adiuvaret in completionem de progressus consilium cuiusque centrum, et promovere comprehensive initiation, executionem et completionem orci investigationis projects ad normam consilii, et
III. Et responsible pro cotidianis procuratio de orci investigationis project et tenere iusto project progressus et communicationis conventus.
IV. Tenere opportune et efficax communicatio cum Pis ut accurate et integrum partum de project - Related Information: et colunt et ponere bonum opus necessitudinem cum investigatoribus (Research centers).
V. Development Norma Development, Formula de Project Management Rules et Sulpicius, et iusto disciplina pro project quadrigis Cras et related curatores.
VI. Negotia assignata a supervisor;
TOTA
I. Bachelor gradus vel superius in orci, velit, biology vel alia related majus, cum Latina cum operantes lingua;
II. Plus quam V annis medicamento orci investigationis opus experientia (cum CRC, CRO opere experientia), magis quam III annos orci project administratione experientia.
III. Working experientia in magna - scale bene - notum Cro societates praeferatur, et independens opus experientia in orci phase, II, II, III projects et experientia in cooperantem cum in - site verificationem est malle.
IV. Nota cum orci investigationis in agro of oncology et autoimmune morbo malle.
V. Aliquam scientia Ich, GCP, technica guidelines ad orci investigationis et pertinet leges et ordinationes in medicamento procuratio.
VI. Project Management Professional Certification (PMP Certificatorium) vel disciplina experientia est malle.
VII. Fortis sensus responsibility, bonum Collaboratio maximi momenti, bonum communicationis et coordinatio artes.
Opus Location: Suzhou
Placere submittere CV ad:Wangxx@hillgengener.com
I. Et responsible pro administratione de orci iudicii projects, portare de comprehensive qualitas imperium et progressus administratione, et ut orci iudicii projects sunt ferri in stricte secundum GCP, Sop, Tentatione protocols et pertinet leges et iudicii protocols et pertineret leges et iudicii;
II. Formulat Management consilia in linea cum project requisitis, adiuvaret in completionem de progressus consilium cuiusque centrum, et promovere comprehensive initiation, executionem et completionem orci investigationis projects ad normam consilii, et
III. Et responsible pro cotidianis procuratio de orci investigationis project et tenere iusto project progressus et communicationis conventus.
IV. Tenere opportune et efficax communicatio cum Pis ut accurate et integrum partum de project - Related Information: et colunt et ponere bonum opus necessitudinem cum investigatoribus (Research centers).
V. Development Norma Development, Formula de Project Management Rules et Sulpicius, et iusto disciplina pro project quadrigis Cras et related curatores.
VI. Negotia assignata a supervisor;
TOTA
I. Bachelor gradus vel superius in orci, velit, biology vel alia related majus, cum Latina cum operantes lingua;
II. Plus quam V annis medicamento orci investigationis opus experientia (cum CRC, CRO opere experientia), magis quam III annos orci project administratione experientia.
III. Working experientia in magna - scale bene - notum Cro societates praeferatur, et independens opus experientia in orci phase, II, II, III projects et experientia in cooperantem cum in - site verificationem est malle.
IV. Nota cum orci investigationis in agro of oncology et autoimmune morbo malle.
V. Aliquam scientia Ich, GCP, technica guidelines ad orci investigationis et pertinet leges et ordinationes in medicamento procuratio.
VI. Project Management Professional Certification (PMP Certificatorium) vel disciplina experientia est malle.
VII. Fortis sensus responsibility, bonum Collaboratio maximi momenti, bonum communicationis et coordinatio artes.
Opus Location: Suzhou
Placere submittere CV ad:Wangxx@hillgengener.com
Senior ipsum, Immunoassay
Job officia
I. Et reus est recognovit et recognovere pertinet test protocols, test records, apparatu operandi operandi ratio et alia documenta in immunoassay coetus, ut ad tentationem actiones in biochemical coetus sunt in imperium
II. Responsible pro development, optimization et confirmatio de immunoassay modi;
III. Et responsible pro Confirmationis et sanatio consilium pro Immunoassay modi involved in processus of technology translatione in comitatu, et exequi confirmationem / convalidandum de ratione analytica modi et scribere operationem in technology translatio;
IV. Test, recordum et collate rudis notitia de R & D samples, stirpe solutions, medium products, complevit products, stabilitatem studium exempla, cellula, etc.
V. Relatorem institutionem et committendas Confirmationis immunoassaSay ad instrumenta et apparatu;
VI. Et responsible pro exercitatione sustentationem de immunoassay - Related instrumenta et exsequendam sanationis consilia;
VII. Et responsible pro inventarium administratione de immunoassay coetus materiae ut continua operatio de coetus.
TOTA
I. Full - tempus adipiscing gradum, postgraduate gradu est malle. II. Saltem V annos experientia in biotechnology in pharmaceutical comitatu;
II. At certe V annorum experientia in Biopharmaceutical analysis in pharmaceutical comitatu;
III. Bonum linguae artes, Collaboratio maximi momenti;
IV. Usus in progressionem et sanationem immuno - Related modi analytica;
V. positivum et studere de opere;
VI. Habere facultatem resistere pressura;
VII. Bonum GMP Awareness, Usus in New medicamento Submission et Official site audits est plus.
Opus Location: Suzhou
Placere submittere CV ad:Wangxx@hillgengener.com
I. Et reus est recognovit et recognovere pertinet test protocols, test records, apparatu operandi operandi ratio et alia documenta in immunoassay coetus, ut ad tentationem actiones in biochemical coetus sunt in imperium
II. Responsible pro development, optimization et confirmatio de immunoassay modi;
III. Et responsible pro Confirmationis et sanatio consilium pro Immunoassay modi involved in processus of technology translatione in comitatu, et exequi confirmationem / convalidandum de ratione analytica modi et scribere operationem in technology translatio;
IV. Test, recordum et collate rudis notitia de R & D samples, stirpe solutions, medium products, complevit products, stabilitatem studium exempla, cellula, etc.
V. Relatorem institutionem et committendas Confirmationis immunoassaSay ad instrumenta et apparatu;
VI. Et responsible pro exercitatione sustentationem de immunoassay - Related instrumenta et exsequendam sanationis consilia;
VII. Et responsible pro inventarium administratione de immunoassay coetus materiae ut continua operatio de coetus.
TOTA
I. Full - tempus adipiscing gradum, postgraduate gradu est malle. II. Saltem V annos experientia in biotechnology in pharmaceutical comitatu;
II. At certe V annorum experientia in Biopharmaceutical analysis in pharmaceutical comitatu;
III. Bonum linguae artes, Collaboratio maximi momenti;
IV. Usus in progressionem et sanationem immuno - Related modi analytica;
V. positivum et studere de opere;
VI. Habere facultatem resistere pressura;
VII. Bonum GMP Awareness, Usus in New medicamento Submission et Official site audits est plus.
Opus Location: Suzhou
Placere submittere CV ad:Wangxx@hillgengener.com
Senior ipsum, cellular asay
Job officia
I. Et reus est revising et revising ad relevant test protocols, test records, apparatu operandi operandi ratio et alia documenta in cellula coetus, ut ad testis actiones in biochemical coetus sunt in coerceri scope;
II. Et responsible pro development, optimization et sanatio de cellula - secundum assays;
III. Et responsible pro drafting dealtical ratio sanatio et verificationis consilium pro internum technology translatio processus, et exequi analytica ratio validation / verificationem secundum probatus, et scribere Validation / verificationem ad standardize et testis operationem de technology translationem
IV. Test, recordum et organize rudis notitia de R & D samples, stirpe solutions, medium products, complevit products, stabilibus exempla, cellula ad normam pertinet Protocols, materiae, et ad normam pertinet in notitia;
V. Responsible pro institutionem et debugging Confirmationis cellula temptationis related instrumenta et apparatu;
VI. Et reus in cotidie sustentationem et reparatione de cellular testis instrumentis et exsequendam validation consilium;
VII. Et responsible pro inventarium administratione materiae in cellular temptationis coetus ut continua operationem de coetus;
VIII. Et responsible pro administratione de cellula ripam ad temptationis, cellula resuscitationem, passaging et congelatio;
IX. Alii officiorum ut assignata a supervisor.
Job requisitis
I. FULL - tempus adipiscing gradum, postgraduate gradu praeferatur;
II. At certe V annorum experientia in Biopharmaceutical analysis in pharmaceutical comitatu;
III. Bonum linguae artes, Collaboratio maximi momenti;
IV. Positive et studere de opere; V. Facultates resistere pressura;
VI. Bonum GMP Awareness, Usus in New medicamento renuntiationes et officialis site audits est plus.
Opus Location: Suzhou
Placere submittere CV ad:Wangxx@hillgengener.com
I. Et reus est revising et revising ad relevant test protocols, test records, apparatu operandi operandi ratio et alia documenta in cellula coetus, ut ad testis actiones in biochemical coetus sunt in coerceri scope;
II. Et responsible pro development, optimization et sanatio de cellula - secundum assays;
III. Et responsible pro drafting dealtical ratio sanatio et verificationis consilium pro internum technology translatio processus, et exequi analytica ratio validation / verificationem secundum probatus, et scribere Validation / verificationem ad standardize et testis operationem de technology translationem
IV. Test, recordum et organize rudis notitia de R & D samples, stirpe solutions, medium products, complevit products, stabilibus exempla, cellula ad normam pertinet Protocols, materiae, et ad normam pertinet in notitia;
V. Responsible pro institutionem et debugging Confirmationis cellula temptationis related instrumenta et apparatu;
VI. Et reus in cotidie sustentationem et reparatione de cellular testis instrumentis et exsequendam validation consilium;
VII. Et responsible pro inventarium administratione materiae in cellular temptationis coetus ut continua operationem de coetus;
VIII. Et responsible pro administratione de cellula ripam ad temptationis, cellula resuscitationem, passaging et congelatio;
IX. Alii officiorum ut assignata a supervisor.
Job requisitis
I. FULL - tempus adipiscing gradum, postgraduate gradu praeferatur;
II. At certe V annorum experientia in Biopharmaceutical analysis in pharmaceutical comitatu;
III. Bonum linguae artes, Collaboratio maximi momenti;
IV. Positive et studere de opere; V. Facultates resistere pressura;
VI. Bonum GMP Awareness, Usus in New medicamento renuntiationes et officialis site audits est plus.
Opus Location: Suzhou
Placere submittere CV ad:Wangxx@hillgengener.com
Senior Engineer, Molecular Deprehensio
Job officia
I. Et reus est revising relevant test protocols, test records, apparatu operandi operandi operandi ratio et alia documenta ad mocecular coetus ad ut testis actiones in Biochemical coetus sunt in potestate;
II. Et responsible pro development, optimization et convalidandum de Molecular testis modi;
3. be responsible for the drafting of analytical method confirmation and validation plan for internal technology transfer, and execute the confirmation/validation of analytical methods according to the approved analytical method confirmation/validation plan, and write confirmation/validation reports to standardise the testing operation of technology transfer;
IV. Test, recordum et organize rudis notitia de R & D samples, stirpe solutions, medium products, complevit products, stabilibus exempla, cellula ad normam pertinet Protocols, materiae, et ad normam pertinet in notitia;
V. Auctor est installation et debugging Confirmationis Molecular testing related organorum;
VI. Responsible pro exercitatione sustentationem de Molecular testis instrumenta et exsecutionem validation consilia;
VII. Responsible pro inventarium administratione de Molecular testis materiae ut continua operatio in coetus;
VIII. Alii officiorum ut assignata per praefectum.
Job requisitis
I. FULL - tempus adipiscing gradu, graduati gradu praefertur;
II. At certe V annorum experientia in Biopharmaceutical analysis in pharmaceutical comitatu;
III. Bonum linguae artes, Collaboratio maximi momenti;
IV. Positive et studere de opere;
V. Potest sustinere quidam gradu pressura, bonum resistentia pressura;
VI. Bonum GMP Awareness, experientia in novo medicamento submission et officialis site audit est commodum.
Opus Location: Suzhou
Placere submittere CV ad:Wangxx@hillgengener.com
I. Et reus est revising relevant test protocols, test records, apparatu operandi operandi operandi ratio et alia documenta ad mocecular coetus ad ut testis actiones in Biochemical coetus sunt in potestate;
II. Et responsible pro development, optimization et convalidandum de Molecular testis modi;
3. be responsible for the drafting of analytical method confirmation and validation plan for internal technology transfer, and execute the confirmation/validation of analytical methods according to the approved analytical method confirmation/validation plan, and write confirmation/validation reports to standardise the testing operation of technology transfer;
IV. Test, recordum et organize rudis notitia de R & D samples, stirpe solutions, medium products, complevit products, stabilibus exempla, cellula ad normam pertinet Protocols, materiae, et ad normam pertinet in notitia;
V. Auctor est installation et debugging Confirmationis Molecular testing related organorum;
VI. Responsible pro exercitatione sustentationem de Molecular testis instrumenta et exsecutionem validation consilia;
VII. Responsible pro inventarium administratione de Molecular testis materiae ut continua operatio in coetus;
VIII. Alii officiorum ut assignata per praefectum.
Job requisitis
I. FULL - tempus adipiscing gradu, graduati gradu praefertur;
II. At certe V annorum experientia in Biopharmaceutical analysis in pharmaceutical comitatu;
III. Bonum linguae artes, Collaboratio maximi momenti;
IV. Positive et studere de opere;
V. Potest sustinere quidam gradu pressura, bonum resistentia pressura;
VI. Bonum GMP Awareness, experientia in novo medicamento submission et officialis site audit est commodum.
Opus Location: Suzhou
Placere submittere CV ad:Wangxx@hillgengener.com