招聘:制剂研发总监(上海)
<p class="MsoNormal" align="left" style="text-align:left;line-height:115%;mso-pagination:widow-orphan"><span style="line-height: 115%; font-family: 宋体; ">目前我集团上海研发中心在招聘一名制剂研发总监,向公司总经理汇报。</span></p><p class="MsoNormal" align="left" style="text-align:left;line-height:115%;
mso-pagination:widow-orphan"><span style="line-height: 115%; font-family: 宋体; ">如有意向者,可投递简历至:<span lang="EN-US">yangl@hansoh.cn</span></span><span lang="EN-US" style="mso-bidi-font-size:
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<p class="MsoNormal" align="left" style="text-align:left;line-height:115%;
mso-pagination:widow-orphan"><span lang="EN-US" style="line-height: 115%; font-family: 宋体; "> </span></p>
<p class="MsoNormal" align="left" style="text-align:left;line-height:115%;
mso-pagination:widow-orphan"><b><span style="line-height: 115%; font-family: 宋体; ">职位介绍:<span lang="EN-US"></span></span></b></p>
<p class="MsoNormal" align="left" style="text-align:left;line-height:115%;
mso-pagination:widow-orphan"><span style="line-height: 115%; font-family: 宋体; ">职位名称:制剂研发总监<span lang="EN-US"></span></span></p>
<p class="MsoNormal" align="left" style="text-align:left;line-height:115%;
mso-pagination:widow-orphan"><span style="line-height: 115%; font-family: 宋体; ">工作地点:上海<span lang="EN-US"></span></span></p>
<p class="MsoNormal" align="left" style="text-align:left;line-height:115%;
mso-pagination:widow-orphan"><span lang="EN-US" style="line-height: 115%; font-family: 宋体; ">Responsibilities:</span></p>
<p class="MsoNormal" align="left" style="margin-left:36.0pt;text-align:left;
text-indent:-18.0pt;line-height:115%;mso-pagination:widow-orphan"><span lang="EN-US" style="line-height: 115%; font-family: 宋体; ">· Developing formulation strategies for
selected generic products, taking into account technical, regulatory and
intellectual property considerations.</span></p>
<p class="MsoNormal" align="left" style="margin-left:36.0pt;text-align:left;
text-indent:-18.0pt;line-height:115%;mso-pagination:widow-orphan"><span lang="EN-US" style="line-height: 115%; font-family: 宋体; ">· Ensuring timely completion of new
product development projects, specifically developing formulations
bioequivalent to the reference products; developing manufacturing processes for
the ANDA registration batches; directing/managing all activities associated
with the registration batch manufacturing; authoring, reviewing and approving
technical documents (protocols, batch records, specifications, development
reports, etc.).</span></p>
<p class="MsoNormal" align="left" style="margin-left:36.0pt;text-align:left;
text-indent:-18.0pt;line-height:115%;mso-pagination:widow-orphan"><span lang="EN-US" style="line-height: 115%; font-family: 宋体; ">· Interacting with Manufacturing,
Validation, and Materials Management to assure smooth scale up of formulations
to commercial scale.</span></p>
<p class="MsoNormal" align="left" style="margin-left:36.0pt;text-align:left;
text-indent:-18.0pt;line-height:115%;mso-pagination:widow-orphan"><span lang="EN-US" style="line-height: 115%; font-family: 宋体; ">· Advising Manufacturing and Quality
Operations of possible impact that deviations from prescribed operating
conditions or procedures may have on products.</span></p>
<p class="MsoNormal" align="left" style="margin-left:36.0pt;text-align:left;
text-indent:-18.0pt;line-height:115%;mso-pagination:widow-orphan"><span lang="EN-US" style="line-height: 115%; font-family: 宋体; ">· Developing, interpreting and
explaining standard practice instructions and procedures, and ensuring that
they are complied with.</span></p>
<p class="MsoNormal" align="left" style="margin-left:36.0pt;text-align:left;
text-indent:-18.0pt;line-height:115%;mso-pagination:widow-orphan"><span lang="EN-US" style="line-height: 115%; font-family: 宋体; ">· Managing, training, and developing
scientific staff. Maintaining effective communication within areas of
responsibility.</span></p>
<p class="MsoNormal" align="left" style="margin-left:36.0pt;text-align:left;
text-indent:-18.0pt;line-height:115%;mso-pagination:widow-orphan"><span lang="EN-US" style="line-height: 115%; font-family: 宋体; ">· Responsibility and authority for
matters such as maintaining quality, accuracy and quantity of work; giving
advice, guidance, and direction; dealing with routine problems; developing
detailed internal work methods; initiating recommendations on personnel
matters.</span></p>
<p class="MsoNormal" align="left" style="margin-left:36.0pt;text-align:left;
text-indent:-18.0pt;line-height:115%;mso-pagination:widow-orphan"><span lang="EN-US" style="line-height: 115%; font-family: 宋体; ">· Monitor and appraise the performance of
personnel reporting to the position</span></p>
<p class="MsoNormal" align="left" style="margin-left:36.0pt;text-align:left;
text-indent:-18.0pt;line-height:115%;mso-pagination:widow-orphan"><span lang="EN-US" style="line-height: 115%; font-family: 宋体; ">· Overseeing and/or collaborating with
external parties involved with formulation development and/or manufacturing.</span></p>
<p class="MsoNormal" align="left" style="mso-margin-top-alt:auto;text-align:left;
line-height:115%;mso-pagination:widow-orphan"><b><span lang="EN-US" style="mso-bidi-font-size:10.5pt;line-height:115%;font-family:宋体;mso-ascii-theme-font:
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text-transform:uppercase;mso-font-kerning:0pt">QUALIFICATIONS</span></b><b><span style="mso-bidi-font-size:10.5pt;line-height:115%;font-family:宋体;mso-ascii-theme-font:
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mso-hansi-theme-font:minor-fareast;mso-bidi-font-family:"Arial Unicode MS";
color:#222222;text-transform:uppercase;mso-font-kerning:0pt">:</span></b><span lang="EN-US" style="line-height: 115%; font-family: 宋体; "></span></p>
<p class="MsoNormal" align="left" style="margin-left:36.0pt;text-align:left;
text-indent:-18.0pt;line-height:115%;mso-pagination:widow-orphan"><span lang="EN-US" style="line-height: 115%; font-family: 宋体; ">· A Science degree is required,
preferably in Pharmaceutics or Chemistry. An advanced degree (PharmD, Masters,
or PhD in a science related discipline) is strongly preferred.</span></p>
<p class="MsoNormal" align="left" style="margin-left:36.0pt;text-align:left;
text-indent:-18.0pt;line-height:115%;mso-pagination:widow-orphan"><span lang="EN-US" style="line-height: 115%; font-family: 宋体; ">· Minimum of 8-10 years of experience
with pharmaceutical development programs, preferably with generic product
development.</span></p>
<p class="MsoNormal" align="left" style="margin-left:36.0pt;text-align:left;
text-indent:-18.0pt;line-height:115%;mso-pagination:widow-orphan"><span lang="EN-US" style="line-height: 115%; font-family: 宋体; ">· Hands on experiences in developing and
manufacturing solid oral dose product, especially modified release products.</span></p>
<p class="MsoNormal" align="left" style="margin-left:36.0pt;text-align:left;
text-indent:-18.0pt;line-height:115%;mso-pagination:widow-orphan"><span lang="EN-US" style="line-height: 115%; font-family: 宋体; ">· Solid understanding of cGMP.</span></p>
<p class="MsoNormal" align="left" style="margin-left:36.0pt;text-align:left;
text-indent:-18.0pt;line-height:115%;mso-pagination:widow-orphan"><span lang="EN-US" style="line-height: 115%; font-family: 宋体; ">· Excellent interpersonal, supervisory,
investigative, and implementation skills.</span></p>
<p class="MsoNormal" align="left" style="margin-left:36.0pt;text-align:left;
text-indent:-18.0pt;line-height:115%;mso-pagination:widow-orphan"><span lang="EN-US" style="line-height: 115%; font-family: 宋体; ">· Must have desire to work and excel in
a rapidly changing, small company environment where a “hands-on” approach is
required.</span></p>
<p class="MsoNormal" align="left" style="margin-left:36.0pt;text-align:left;
text-indent:-18.0pt;line-height:115%;mso-pagination:widow-orphan"><span lang="EN-US" style="line-height: 115%; font-family: 宋体; ">· Must have strong leadership abilities.</span></p>
<p class="MsoNormal" align="left" style="margin-left:36.0pt;text-align:left;
text-indent:-18.0pt;line-height:115%;mso-pagination:widow-orphan"><span lang="EN-US" style="line-height: 115%; font-family: 宋体; ">· Requires the ability to influence
others and communicate effectively, written and orally, both internally and
externally.</span></p>
<p class="MsoNormal" align="left" style="margin-left:36.0pt;text-align:left;
text-indent:-18.0pt;line-height:115%;mso-pagination:widow-orphan"><span lang="EN-US" style="line-height: 115%; font-family: 宋体; ">· Must possess excellent written and
verbal communication skills. Requires</span></p>
<p class="MsoNormal" align="left" style="margin-left:36.0pt;text-align:left;
line-height:115%;mso-pagination:widow-orphan"><span lang="EN-US" style="line-height: 115%; font-family: 宋体; ">the ability to prepare and review technical reports</span></p>
<p class="MsoNormal" align="left" style="margin-left:36.0pt;text-align:left;
text-indent:-18.0pt;line-height:115%;mso-pagination:widow-orphan"><span lang="EN-US" style="line-height: 115%; font-family: 宋体; ">· Requires the ability to motivate,
lead, and develop departmental staff from an organizational as well as
technical perspective</span></p>
<p class="MsoNormal" align="left" style="margin-left:36.0pt;text-align:left;
text-indent:-18.0pt;line-height:115%;mso-pagination:widow-orphan"><span lang="EN-US" style="line-height: 115%; font-family: 宋体; ">· Demonstrated ability to work
effectively in a team environment, manage multiple priorities, exercise sound
judgment, be well organized, take initiative, be flexible, work well under
pressure and produce accurate and timely work.</span></p>
<p class="MsoNormal" align="left" style="margin-left:36.0pt;text-align:left;
text-indent:-18.0pt;line-height:115%;mso-pagination:widow-orphan"><span lang="EN-US" style="line-height: 115%; font-family: 宋体; ">· Fluent in both Chinese and English.</span></p>
<p class="MsoNormal" align="left" style="text-align:left;line-height:115%;
mso-pagination:widow-orphan"><b><span lang="EN-US" style="line-height: 115%; font-family: 宋体; "> </span></b></p>
<p class="MsoNormal" align="left" style="text-align:left;line-height:115%;
mso-pagination:widow-orphan"><b><span style="line-height: 115%; font-family: 宋体; ">企业介绍:</span></b><span lang="EN-US" style="line-height: 115%; font-family: 宋体; "><a href="http://www.hansoh.cn/" target="_blank"><span style="color:blue">www.hansoh.cn</span></a></span></p>
<p class="MsoNormal" align="left" style="margin-bottom:12.0pt;text-align:left;
line-height:115%;mso-pagination:widow-orphan"><span style="line-height: 115%; font-family: 宋体; ">豪森医药创建于<span lang="EN-US">1995</span>年<span lang="EN-US">7</span>月,现已发展为集化学、生物药物研究,医药中间体、原料药合成、制剂制造和产品销售于一体的创新型医药集团。<span lang="EN-US">2011</span>年期末职工总数超过<span lang="EN-US">4000</span>人。集团总部及制造基地位于风光秀丽的花果山下、国家级连云港开发区新医药产业园内,在上海、北京设有创新药物研发中心和临床研究中心。豪森医药集团是国家重点高新技术企业和中国制药工业百强企业,综合竞争力、经济效益位居全国同行业前列。<span lang="EN-US"><br>
</span>豪森拥有遍布全国的销售网络和专业化的营销团队,专业化的营销模式使豪森品牌的市场价值不断提升,市场规模不断扩大。目前,江苏豪森集团在抗肿瘤、精神、内分泌、抗生素及消化道类等五大疾病治疗领域有<span lang="EN-US">40</span>多个品种进入市场销售,<span lang="EN-US">2011</span>年销售额近<span lang="EN-US">40</span>亿元。<span lang="EN-US"></span></span></p>
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