We are looking to hire a Drug Product Manufacturing Associate for our client in Carlsbad. They are in the biopharmaceutical and molecular diagnostics industries looking for someone with experience performing tasks and operations relevant to the bulk formulation and/or filling operations required for sterile production of liquid injectable pharmaceutical products under cGMP regulations in Drug Product Manufacturing. 

Compensation: $20-24/hr depending on experience

Schedule: Monday thru Friday overtime and weekends as needed. Flexible start time between 7am - 9am

Duties and Responsibilities:

• Perform various routine manufacturing tasks under the direction of internal SOP's and cGMP guidelines
• Prepare material components for manufacturing operations
• Document steps clearly and completely in production batch records, logbooks and other controlled forms
• Participate in inspection readiness activities
• Perform basic arithmetic and algebraic computation
• Maintain cleanliness of areas and equipment
• Assist senior level personnel in bulk drug formulation using a variety of lab equipment including mixers, balances, pH meters, etc., gowned in accordance with Class C (ISO 7) conditions
• Assist senior level personnel in sterile filtration activities, gowned in accordance with Class C (ISO 7) conditions
• Assist senior level personnel in sterile filling of a multitude of solutions including drug product, media, buffers, using an automated filling and closing machine, gowned in accordance with Class C (ISO 7) conditions
• Collect and dispose of lab wastes according to established procedures
• Collaborate in continuous improvement activities

Education/Experience Requirements:

• High school diploma or equivalent with 1 - 2 years relevant experience is required, a Bachelor's in an Engineering discipline or Life Science field preferred
• Time and project management skills with the ability to multi-task are essential
• Must be able to effectively communicate within department and cross-functionally with other divisions
• High level of personal and professional integrity and trustworthiness with a strong work ethic and the ability to work independently with minimal direction
• Experience in a growth-oriented, cGMP contract manufacturing organization with a focus on compliant execution of business, is a plus