JT093 - MANUFACTURING ASSOCIATE

QUALITY CONSULTING GROUP, a leader in the pharmaceutical, biotech, medical devices, and manufacturing industry, is looking for a talented, highly motivated and enthusiastic to join our team. In this role, you’ll work with a highly enthusiastic team, contributing in a world-class manufacturing industry in Puerto Rico & USA.

Responsibilities:        

• Responsible for manufacturing and support activities in the drug product Formulation Development Lab, a pilot scale drug product manufacturing facility.
• Support manufacturing process readiness activities.
• Carry out manufacturing unit operations including blending, granulation and tablet compression.
• Perform visual inspection of drug product.
• Maintain facility and equipment documentation (equipment/room logbooks).
• Maintenance of raw materials & consumables inventory.
• Supporting day to day operational needs of the facility.
• Dispensing and handling of hazardous raw materials.
• Hands-on cleaning, sanitization, and setup of manufacturing equipment.
• Operating machinery and tools while complying with all safety protocols and operational standards.
• Preparation of batch records for use in GMP campaigns and planning manufacturing activities.
• Identify, recommend, and implement improvements related to routine functions.
• Collaborate in a multidisciplinary team with process development chemists, engineers, analysts, and facility staff.

Qualifications:

• Associate degree or High school/GED + 1 year of related work experience
• One year of experience in a manufacturing or distribution environment where following procedures was essential.
• Understanding of unit operations for the manufacture of synthetic drug products (i.e. granulation, roller compaction, drying, milling, blending, compression, encapsulation and film coating)
• Ability to work well in a cross functional team environment.
• Proficiency with basic technology such as laptops and tablets (including iPads) are required.
• Prior exposure to GMP-regulated industries, electronic batch records, DeltaV, or LIMS is a plus but not required, as training will be provided.
• FULLY ONSITE AT USTO
• DAY SHIFT POSSIBLE TO TRANSITION TO SWING BUT NOT CONFIRMED
• Shift: 4x a week - 6AM to 5PM

Quality Consulting Group, LLC is an equal opportunity employer, and all qualified applicants will receive consideration for employment without regard to race, color, religion, sex, sexual orientation, gender identity, genetic information, national origin, protected veteran status, disability status, or any other characteristic protected by law.

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