Manufacturing Technician II​/III

August Bioservices is seeking to hire experienced manufacturing technicians to support our growing formulations and filling teams. Headquartered in Nashville, TN - one of the fastest-growing and most exciting cities in the United States - August Bioservices is a privately-owned, high-growth, and high-impact Contract Development Manufacturing Organization (CDMO).  As a US-based outsourcing partner that provides a wide array of expert drug discovery, drug formulation, and drug manufacturing services to pharma and biotech companies of all sizes, we play a vital role in the global pharmaceutical industry.

Our work is instrumental in helping to develop molecules today that can become the life-changing therapies of tomorrow. For those seeking dynamic opportunities, rewarding career paths and a chance to make a difference in global health, come grow with August!

Responsibilities

* Perform routine cleaning and sanitization of production areas to maintain a controlled and compliant environment.

* Complete training for routine cleaning and sanitization of production areas to maintain a controlled and compliant environment.

* Prepare and transfer materials and components for production using proper sanitization techniques and aseptic handling practices.

* Complete training to prepare and transfer materials and components for production using proper sanitization techniques and aseptic handling practices.

* Utilize proper aseptic techniques in Grade B/C/D and CNC environments during all tasks.

* Adhere to safety and environmental health standards, including proper use of PPE.

* Perform Inspection, labeling, and packaging of vials, IV bags, and syringes.

* Perform dispensing and formulating raw materials for aqueous and non-aqueous products, ensuring accuracy and compliance with batch records.

* Perform preparation of equipment for use using sterilization equipment such as autoclaves and HEPA cabinets.

* Operate and maintain equipment used across all production processes, including formulation, filling, sterilization, inspection, and packaging with support and oversight from other Manufacturing team members.

* Complete all GMP documentation, including batch records, protocols, and deviations, adhering to Good Documentation Practices (GDP).

* Collaborate cross-functionally with production, QA, QC, engineering, validation, and maintenance teams as required.

* Recognize and report deviations, potential issues, or equipment malfunctions to the management team.

* Load, operate, and unload sterilization equipment, such as autoclaves, terminal sterilizer, and HEPA transfer carts.

* Maintain consistent presence on Manufacturing floor and support all teams in production as needed.

* Assist with set up and operate filling lines and associated equipment, including mixers, tanks, pumps, autoclaves, and HEPA transfer carts.

* Assist with troubleshooting equipment breakdowns.

Required

Skills and Qualifications

* High School Diploma or equivalent required. An associate degree in a technical field or a bachelor's degree in biological, chemical sciences, or engineering preferred but not required.

* 1+ years in pharmaceutical manufacturing environments.

* Mechanical aptitude to operate and troubleshoot a variety of equipment and instruments.

* Understanding of GMP and GDP standards.

* Strong attention to detail, with the ability to follow SOPs, complete documentation tasks accurately.

* Basic computer skills and familiarity with technical documentation.

* Mathematical skills for measurements and calculations (e.g., volume, weight).

* Physical ability to raise arms over head, stoop, stand, climb, and lift 30-50 lbs.

* Effective verbal and written communication skills.

* Prolonged periods of standing, walking, or working in a cleanroom environment.

* Ability to wear fully protective gowning for extended periods.

* Must be able to lift and transport materials weighing up to 50 lbs.

* Ability to consistently arrive at work for on time for shifts as assigned.