居住国家 美国
居住城市 Pennsville, New Jersey
功能区域 Operations
工作组 Supply Chain
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
SUMMARY:
The incumbent is responsible for receiving and sampling raw materials (bulk and non-bulk) and for shipping of materials, for the processing of hazardous waste drummed materials and performs general warehouse duties including but not limited to labeling, keeping inventory, staging, and maintaining the housekeeping of the warehouse and surroundings up to cGMP standards. Precise computer and data entry is 50% of the work for this position.
ESSENTIAL DUTIES, RESPONSIBILITIES AND ACCOUNTABILITIES:
Receiving:
• Receives raw materials, both bulk and non-bulk, inter-plant, W.I.P., and returns, completes paperwork, segregates material by batch or lot number, re-weighs critical raw materials and labels, notifies QC Lab of deliveries for analysis, inspects shipment for proper labeling, cleanliness, and damage.
• Enters receipts into computer, verifies PO’s for distribution of incoming UPS, FedEx, DHL and VWR packages.
Shipping:
• Loads trucks, compares shipping document with outgoing material, completion of paperwork, such as driver’s signature and date and processing of paperwork.
• Responsible for material movement between Warehouse II, storage pads and Production.
• May off load trucks, assist or move material in Warehouse I.
Environmental:
• Stages drums for environmental labeling and sampling, stage drums for disposal in a segregated area in accordance with the Inventory Reduction Program and load drums on the truck.
General:
• Responsible for housekeeping in and around warehouses, Pad 6 and the Tank Farm to maintain a safe, compliant and 5s cGMP facility.
• Maintains proper inventory control, order and distribution of factory supplies.
• Conducts cycle counts and assist in physical inventories, data entry of material movement and location where material can be found.
• Adheres to personal moral, ethical, legal, and behavioral conduct in compliance with the Siegfried Code of Conduct.
• Adheres to all applicable SHE and CGMP regulations.
• Delivers paper to all printer locations onsite.
• Incumbent will be expected to work during inventory preparation year-end Inventory and reconciliation
• Offload Poly, Steel and Fiber drums trailers.
您的个人资料
EDUCATION AND EXPERIENCE:
• Must have a high school diploma or equivalent.
• Must have 5 or more years of experience in cGMP compliant warehousing.
• Must be able to read and write legibly and perform simple arithmetic.
• Having experience in chemical operations is a plus.
OTHER REQUIREMENTS:
• Must know how to operate industrial in-plant vehicles.
• Must be able to do physical work such as climbing stairs, lifting containers weighing up to 100 lbs., and rolling containers weighing up to 400 lbs.
• Must be able to pass DOT training.
• Must be able to pass ERT training to handle spills.
• Must be willing to work Overtime.
Siegfried USA will explore and provide reasonable accommodations to assist any qualified individual with a disability in performing the essential functions of his/her job. Please speak with HR should you require an accommodation or have any questions.
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。
我们在做什么Pennsville
Pennsville is our drug substance manufacturing site for the US mar-ket and provides spray drying operations globally.
Main activities
- Pilot and commercial manufacturing of drug substances (APIs) and related intermediates
- All fully cGMP and SHE compliant
Features
- 3 GMP pilot suites: 0.1–2 m³ reactors
- 200m3 commercial capacity: 1–10 m³ reactors
- Successful transfer of new products to the commercial scale - Powerful rectification
- Spray drying in pilot and commercial scale for both isolation and dispersion technology
- Micronization in pilot and commercial
Strategic importance
- CMO for innovative drug substances and manufacturer of our opiates portfolio for the US market