Pharmaceutical Development Technician II Position Available In Hall, Georgia
Tallo's Job Summary: The Pharmaceutical Development Technician II position at Bend Bioscience in Gainesville, GA requires at least 5 years of related pharmaceutical manufacturing experience, including 2 years in solid oral dosage manufacturing. Responsibilities include weighing, dispensing, operating equipment, testing materials, maintaining cleanliness, and assisting in training. Compliance with cGMP procedures is essential. This is an Equal Opportunity Employer.
Job Description
Pharmaceutical Development Technician II Bend Bioscience Gainesville, GA 30501 At Bend Bioscience, our
Core Values Shape Everything We Do:
AUTHENTIC
•Be vulnerable, build trust CURIOUS•Ask questions, be adaptable, speak up
ACCOUNTABLE
•Own it, meet commitments, communicate transparently
COLLABORATIVE
•Engage others, stay open-minded
FLEXIBLE
•Listen actively, be thoughtful, make informed decisions CARE•Be passionate, act with integrity
BLAZE TRAILS
•Push boundaries, challenge constraints
EXCELLENCE
•Learn, improve, create value FOCUS•Pay attention to details, stay determined, deliver exceptional service Join Bend Bioscience and be part of a dynamic team that makes a real difference. How You Will Make an
Impact:
Weigh, dispense and keep manual inventory of raw and in-process materials and finished product. Set up, operate and clean equipment such as Wurster fluid-bed processors, rotor granulators, tablet presses, Fitzmills, V-blenders, hard gelatin encapsulation machines, or capsule checkweighers. Sample and physical testing of research in-process materials, e.g. sieve analysis, particle size analysis, loss-on-drying, microscopy, etc. Complete written documentation of work performed such as logbook entries, batch records, and material tracking forms. Maintain cleanliness of PD suite including mopping, disposing of garbage and general housekeeping duties. Conduct physical inventories for controlled/non-controlled substances. Monitor facilities and equipment on a routine basis, such as magnehelic gauges, water systems and stability chambers. Assist in execution of IOQs for processing equipment. Assist in training manufacturing operators for new product transfers. Attend cGMP training sessions and comply with site-wide and departmental procedures including but not limited to change control, documentation, deviation reporting, cGMP compliance, safety and electronic data security. What You Will Bring to the
Role:
High School Diploma or General Education Degree (GED). At least 5 years’ experience in related pharmaceutical manufacturing work, including at least 2 years’ experience in solid oral dosage pharmaceutical manufacturing work. Equal Opportunity Employer/Protected Veterans/Individuals with Disabilities This employer is required to notify all applicants of their rights pursuant to federal employment laws. For further information, please review the Know Your Rights notice from the Department of Labor.
