Pharmaceutical Development Technician II

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.