葫芦岛招聘

As an employee of Boehringer Ingelheim, you will actively contribute to the discovery, development and delivery of our products to our patients and customers. Our global presence provides opportunity for all employees to collaborate internationally, offering visibility and opportunity to directly contribute to the companies' success. We realize that our strength and competitive advantage lie with our people. We support our employees in a number of ways to foster a healthy working environment, meaningful work, diversity and inclusion, mobility, networking and work-life balance. Our competitive compensation and benefit programs reflect Boehringer Ingelheim's high regard for our employees

Description:
?Is responsible for establish, maintain and continuously improve the performance and reliability of the testing of starting material and product, deviation handling and equipment and reagent management etc.under corporate management guideline and cGMP regulation to ensure product quality in accordance with BI SOP/cGMP/Registered Specification
?To obey and improve all procedure to maintain a high quality level and competitive cost
?To ensure QC department to maintain the stable support to Value Stream

Duties & Responsibilities:
?Be responsible for carrying out daily sampling and testing for raw materials, packaging materials, intermediates, bulk products, finished products and stability study product, testing for purified water and waste water, finish the environment monitoring etc，ensure to complete testing and releasing timely
?Review API / excipients / packaging material testing result to ensure that they comply with testing standard and GMP requirement e.g. DI
?Establish Testing Specifications for Raw Materials and Packaging Materials, and relevant SOPs/Forms according to given instructions, ensure to comply with GMP, regulatory and BI requirements
?Execute lab equipment qualification and maintenance, ensure to perform all tests smoothly
?Update SOP related to Product quality function according to business needs and regular review to ensure comply with GMP and BI global requirement
?As core member to support the Analytical Method Transfer and AMV implementation to support the new product launch and transfer
?Support the action / project to monitor or reduce the rate of lab error e.g. OOS
?Establish and optimize the testing procedure creatively including management of equipment, glassware, reagent etc to continues improve the productivity and cost saving with comply with requirement from SFDA and company
?Coordinate, monitoring and support the other analysts to comply with GMP, EHS, and 5S in daily work
?Focus on Chemical-lab related task. And be a Micro-lab backup of related task
?Fulfill the other temporary task assigned by QC Manager
?To participate organization activities as key person
?Provide technical skill training to other analysts

Requirements:
?Bachelor degree or above in GMP concept, Pharmaceutical or related discipline
?Good English writing, reading, listening and speaking
?Experience of working in a pharmaceutical quality control environment
?Minimum of 3 years experience of QC
?Be good at HPLC, GC, UV, IR etc
?Good knowledge of GMP
?Good team player
?Be able to work under pressure
?Good coaching ability
?Can create new idea or innovative method to mutilple functions

Our Culture:
Innovative medicines for people and animals have for more than 130 years been what the research-driven pharmaceutical company Boehringer Ingelheim stands for. Boehringer Ingelheim is one of the pharmaceutical industry’s top 20 companies and to this day remains family-owned. Day by day, our employees create value through innovation for the three business areas human pharmaceuticals, animal health and biopharmaceutical contract manufacturing.
Boehringer Ingelheim operates globally with approximately 50,000 employees. Since we are privately held, we have the ability to take an innovative, long-term view. Our focus is on scientific discoveries and the introduction of truly novel medicines that improve lives and provide valuable services and support to patients and their families. Employees are challenged to take initiative and achieve outstanding results. Ultimately, our culture and drive allows us to maintain one of the highest levels of excellence in our industry

关于勃林格殷格翰
加入勃林格殷格翰，与我们一起携手并肩，共创未来。我们深信每一位员工的成长都将铸就公司的发展，每一位员工的努力也都将成就公司的美好明天。130余年来，研发驱动型制药公司勃林格殷格翰作为全球前20大制药企业之一，持续致力于人用药品、动物保健和生物制药合同生产三大业务领域，力争为人类和动物带来更多健康。加入勃林格殷格翰，将是您实现“创新展现价值”的绝佳机会！在工作中，您将通过与内外部伙伴的通力合作，站在知识迭代的最前沿；科研过程中，您将不断探索新型科学发现，切实提高全人类的生活质量；与此同时，您也将助力公司成为未来行业当之无愧的领导者。

我们的业务正处在持续高速发展之中，是中国业内发展最快的公司之一。我们诚邀您加入勃林格殷格翰，共同携手向前，成为实现2025愿景的一份子。

作为业内的领导企业，热情、创新和独立是驱动我们不懈前行的动力，我们为每一位努力热忱、恪尽职守的员工提供成长机会，实现其个人价值。作为连续七年通过“中国杰出雇主”认证的企业，我们通过提供高质量的职业发展规划、参与或领导国际项目的机会，为每一位员工的成功之路夯实基础。
 让我们彼此成就，引领未来！

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行为准则
-责任心：即使情况不明朗，我们总是在自己的决策和行为中展现主人翁精神
-敏锐度：面对内外部变化时，我们以开放的心态快速应对
-内部企业家精神：我们与客户携手构筑创新理念，以应对瞬息万变的市场

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