一般信息

居住国家 美国

居住城市 Grafton, Wisconsin

功能区域 Operations

工作组 Production

雇佣类型 长期合约

工作时间 全职

齐格弗里德(Siegfried)在全球各地为员工提供国际化的激动人心的职业机会。 我们促进多学科合作,并鼓励我们的员工积极塑造和影响他们的职业生涯。 这种方法,加上我们动态的工作环境,使齐格弗里德成为有吸引力的雇主。

你的角色

The Quality Control Analyst II is responsible for performing routine and non-routine analytical chemistry assays of raw materials, in-process samples, finished APIs, and stability samples. This role also participates in special projects, method development/transfers and cleaning study qualifications.

Essential job duties

  1. Perform analytical testing for incoming, in-process and final products, and stability samples using equipment such as balances, pipettes, pH meter, UV/Visible spectrophotometer, Total Organic Carbon analyzer, etc.
  2. Perform chromatography (HPLC/GC, UPLC) with minimal qualification and training, wet chemistry assays, analytical chemistry assays, HPLC, GC, IR, UV, etc. and raw material testing and/or sampling
  3. Back up for QC analytical instrument maintenance and calibration
  4. Perform QC general laboratory equipment maintenance, laboratory housekeeping and preparation of the laboratory for audits
  5. Perform or assist with QC method qualifications, transfers and validations
  6. Perform QC method development
  7. Perform cleaning validation studies
  8. Assist with the evaluation of new equipment and processes
  9. Assist in the review of QC data and provide summaries to management as needed
  10. Assist QC Management, as needed, in the completion of OOS, deviations, and CAPAs investigations for QC
  11. Backup for QC analytical sample receipt for internal testing, outside laboratory testing, login, processing, shipment, tracking, distribution of test results, and closure

您的个人资料

Education, experience, certification and licensures

Required

  • Bachelor’s degree in Chemistry or related field
  • Minimum 3-5 years’ experience in pharmaceutical industry environment or equivalent combination of education and experience

Preferred

·         Experience working in cGMP or GLP pharmaceutical industry environment

Knowledge, skills and abilities

1.       Excellent verbal and written communication skills, including the ability to effectively present information and respond to questions from groups of managers, clients, customers, and the general public

2.      Ability to meet deadlines and work under pressure with limited supervision

3.       Strong time management and organizational skills with the ability to multi-task and manage multiple projects independently

4.      Ability to read, analyze, and interpret general business periodicals, professional journals, technical procedures, or governmental regulations

5.      Ability to write reports, business correspondence, and procedure manuals

6.      Ability to apply advanced mathematical concepts such as exponents, logarithms, quadratic equations, and permutations

7.       Ability to apply mathematical operations to such tasks as frequency distribution, determination of test reliability and validity, analysis of variance, correlation techniques, sampling theory, and factor analysis

8.      Ability to define problems, collect data, establish facts, and draw valid conclusions

9.      Ability to interpret an extensive variety of technical instructions in mathematical or diagram form and deal with several abstract and concrete variables

10.  Proficient use of computer software, including Microsoft Office Suite and instrument manufacture-based systems

11.   Knowledgeable in FDA GMPs (21 CFR, 211, 820, and/or 600); ISO 9001 and 13485 a plus

Physical requirements

The physical demands described here are representative of those that must be met by an employee to successfully perform the essential functions of this job. Reasonable accommodations may be made to enable individuals with disabilities to perform the essential functions.

While performing the duties of this job, the employee is regularly required to stand; walk; or sit; use hands to finger, handle, or feel; and talk or hear. The employee frequently is required to reach with hands and arms. The employee is occasionally required to climb or balance; and stoop, kneel, crouch, or crawl. The employee must occasionally lift and/or move up to 50 pounds. Specific vision abilities required by this job include close vision, and ability to adjust focus.


在我们公司工作

齐格弗里德的工作环境充满活力和国际化。 凭借高度专业和积极进取的团队,该公司在面向未来的业务领域中运营。 齐格弗里德(Siegfried)拥有独特的文化,可以利用文化差异创造竞争优势。 齐格弗里德(Siegfried)最优先考虑的是提供一个灵活,多样且无歧视的工作环境,在此环境中,员工可以个人发展和专业发展,推动创新并提供卓越的绩效。 我们努力提供一个工作环境,使员工可以承担具有挑战性的工作和相关的职责,从而最好地服务于其个人和技术发展,并可以从我们公司的成功中受益。 公司有关薪酬和职业发展机会的规定适用于所有齐格弗里德工厂。 额外的就业条件受所在地的具体情况,法律和习俗的约束。

我们是谁

在人们的生活中–全球

齐格菲集团(Siegfried Group)是全球领先的定制开发和制造组织(CDMO)之一,致力于开发和生产活性药物成分(API),中间体和最终剂型。作为我们的核心竞争力,我们成功地将化学和制药能力整合到一个商业模式中。

齐格菲(Siegfried)这个名字代表着最高的质量,效率,灵活性和安全性。我们的业务遍及欧洲,亚洲和北美,从主要的国际制药公司到小型生物制药组织,为广泛的全球客户群提供服务。我们为他们开发和生产大规模的产品创新产品到成品。我们将报价无缝整合到客户的价值链中。我们的综合服务范围涵盖从早期研究与开发服务(例如合成,放大,配方开发,稳定性研究和方法开发)一直到制造服务,从用于临床试验目的的临床前研发材料到商业生产。

我们能够生产约1500种注册药物中的约200种。此外,我们生产的咖啡因占全球需求量的20%。因此,将近10亿个人与Siegfried产品接触。

What we do in Grafton

The Siegfried Acceleration Hub in Grafton specializes in early-phase development and manufacturing services, including services for projects with highly potent APIs.

Competencies

·         Early-phase development and manufacturing