Job Description
Job DescriptionAugust 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.