Manufacturing Associate I (Manufacturing/Quality)

Immediate need for a talented Manufacturing Associate I (Manufacturing/Quality). This is a 14+months contract opportunity with long-term potential and is located in Pearl River, NY(Onsite). Please review the job description below and contact me ASAP if you are interested.
 
Job ID:25-89844
 
Pay Range: $23 - $25/hour.  Employee benefits include, but are not limited to, health insurance (medical, dental, vision), 401(k) plan, and paid sick leave (depending on work location).
 
Key Responsibilities:

• In depth understanding of techniques and processes being executed on routine basis.
• Responsible for all aspects of media, buffer and solution formulation including equipment preparation (CIP and SIP), appropriate use of raw materials and components (FIFO), weighing and dispensing of raw materials and intermediate solutions, material sampling for applicable analytical testing, filter integrity testing, etc.
• Responsible for the operation and maintenance of ancillary equipment such as pH / conductivity meters, osmometer, tube welder, tube sealer, peristaltic pumps, etc.
• Interacts with other departmental personnel to assist in resolving manufacturing quality issues.
• Technician should have the ability to manage and analyze manufacturing data.
• Ensure good documentation practices (GDP) in execution and reviews of production records.
• Responsible for all required cGMP training including additional training assigned by their manager.
• Participates in the cleaning of the cGMP facility in accordance with sanitary maintenance SOP.
• Follows established SOPs for the flow of materials, personnel, and equipment in and out of the cGMP facility.
• Work a flexible work schedule, weekends and holidays as required, and as needed by department.
• Work with Compliance regarding notification of deviations and CAPAs as they occur and provides information during investigations.
• Other duties as they are required.

Key Requirements and Technology Experience:

• Key Skills: DNA Seq, Baculovirus, Cell Culture, Molecular Biolog .
• High School degree with at least 2 years of work experience, or training within a cGMP manufacturing environment .
• General knowledge of cGMP, GDP, SOP’s .
• Good communication and social skills .
• Basic understanding of the Baculovirus Expression Vector System (BEVS) manufacturing process is desired but not required .

Our client is a leading Pharmaceutical Industry, and we are currently interviewing to fill this and other similar contract positions. If you are interested in this position, please apply online for immediate consideration.
 
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