Bryllan LLC is a privately owned, rapidly growing Contract Manufacturing Organization (CMO) that has designed a unique sterile filling and containment platform for multi-product filling of cytotoxic, potent, live virus and vaccine, and hormone drug products. We offer a rewarding work environment while maintaining a small company, employee-focused atmosphere. Bryllan differentiates itself from our competitors by living our values of Integrity, Quality and Service.
We are currently seeking experienced pharmaceutical production technicians to join our operations team. Technicians will be responsible for all aspects of production, including dispensing, formulation, aseptic filling and packaging of our customers' product.
Successful candidates exhibit a strong knowledge of cGMP, desire to work in a team environment, seek opportunities for continuous improvement, and perform to the highest ethical standards. They may be required to lift up to 50 pounds, stand for long periods of time and wear appropriate PPE including proper gowning for entry into controlled areas. Applicants should also possess at least 6 years in a related environment through a combination of education and work experience (BS + 2 yrs. experience | Associates + 4 yrs. | HS + 6 yrs.)
All members of our Operations teams are expected to follow detailed SOP's and MBR's; maintain clean, safe and efficient work environments; comply with all regulatory and company specific safety and quality regulations; troubleshoot basic mechanical operations and equipment; operate and navigate equipment functionality through routine interaction with Human-Machine Interface or Supervisory Control and Data Acquisition systems; complete and review appropriate production and batch documentation accurately and consistently; perform equipment change-overs and cleaning for manufacturing; utilize knowledge and experience to improve procedures and processes; collaborate in a team environment including treating everyone with respect and courtesy and freely sharing knowledge. Selected candidates must possess a functional understanding of cGMP's and the impact of deviation from controlled processes or procedures.
Production Technicians will specifically:
Verify identity and quantity of components/materials for use in manufacturing.
Initiate and monitor equipment cycles (CIP, SIP, Decontamination, etc.)
Record GMP data on controlled documentation accurately, precisely, contemporaneously.
Transport hazardous and non-hazardous materials into/out of manufacturing area.
Wash, sanitize, and utilize material carts / bins / totes.
Complete and maintain training records within expected timelines.
Load and un-load materials into and out of rapid transfer ports, isolators.
Additionally, we seek colleagues who have the ability to develop and communicate corrective and preventative actions for process deviations; understand abstract concepts such as sterility and contamination; possess strong mathematical and organizational skills; exude honesty, integrity and commitment to the highest legal and ethical standards; work with minimal supervision; demonstrate pride in their work and an uncompromising commitment to quality.
As Bryllan LLC continues to grow, we offer a unique opportunity for individuals to grow and develop along with us. Our culture promotes teamwork, accountability, respect, continuous improvement, development and open communication. We encourage the use of knowledge and experience to mentor others and identify ways to improve our processes. Bryllan colleagues enjoy a comprehensive benefits package and 401k program.
This posting is specifically for candidates with experience in pharmaceutical manufacturing. If you have not worked in pharmaceutical manufacturing, we encourage you to share your interest by applying to our general posting Growing Pharmaceutical CMO for future opportunities.