Manufcaturing Techician

Responsibilities

With direct supervision this individual will perform routine clinical manufacturing operations at the Client Manufacturing Facility, ensuring safe, efficient and cGMP-compliant operations at all times.

Responsibilities include but are not limited to operation of production equipment in the areas of weigh/dispense, solution preparation, equipment CIP/COP and small parts cleaning, and materials stocking in manufacturing suites.

Operates production equipment according to SOPs for the production of clinical products. Requires interaction with support groups (Facilities, QC, QA, Materials Management, EHS) to ensure accurate completion of activities.

• Minimum 1-3 Years of industry experience
• Must possess mechanical and scientific aptitude and be able to clearly and thoroughly document all work on existing forms and records.
• Proficient in Microsoft Office (Word, Excel, Visio)
• Safety and the ability to maintain a compliant, highly effective and efficient product environment are critical.
• High level of attention to details in both operations and documentation is required.
• Must be able to execute strenuous, sometimes repetitive physical work on manufacturing shift schedule in classified cleanroom environment.
• Ability to lift objects up to 50 lbs, and push/pull objects including bulk materials up to 250 lbs with assistance.
• Typically, will lift less than 20 pounds.
• Strong time management skills, attention to detail, and an ability to work in a team setting required. Excellent communication skills

• Minimum Associates or Bachelor's degree in science
• Biotech Certificate and/or Manufacturing Certificate preferred