Manufacturing Specialist I/II, Downstream

KBI Biopharma • Durham, NC

12d

About The Position

At KBI Biopharma, we are advancing science and accelerating breakthroughs. As a global leader in biopharmaceutical development and manufacturing, we empower life science companies to bring new medicines and vaccines to the world faster. Explore your potential at KBI, where innovation meets impact. Position Summary This position will provide technical support activities for GMP Manufacturing Operations in a multi-product, large scale, biopharmaceutical facility. This role will support, but not limited to the following: Drafting, routing, and revision of manufacturing batch records, procedures, supporting records. Manufacturing process support during on-going shop floor execution, when required. Support new equipment enrollment efforts from purchasing to qualification activities. First line of defense for manufacturing events. The candidate will assess the event and provide immediate corrective actions. Lead implementations for corrective and preventive actions. Point of contact for laboratory equipment supporting manufacturing operations, troubleshooting, vendor calls, equipment repair coordination, operational changes and system qualifications. Support safety initiatives, compliance & quality requirements.

Requirements

• Specialist I: High School Diploma with 5+ years’ related industry experience (Downstream/Purification operations preferred); Bachelor’s Degree in a related scientific or engineering discipline preferred with 2+ years’ related industry experience; Master’s degree in a related scientific or engineering discipline preferred with 0+ year’s related industry experience.
• Specialist II: High School Diploma with 8+ years’ related industry experience (Downstream/Purification operations preferred); Bachelor’s Degree in a related scientific or engineering discipline preferred with 4+ years’ related industry experience; Master’s degree in a related scientific or engineering discipline preferred with 2+ year’s related industry experience
• Language Ability Ability to read and interpret English documents such as safety rules, operating and maintenance instructions, procedure manuals, batch and production records. Ability to write routine GMP documents. Ability to speak effectively on front of internal groups.
• Reasoning Ability Ability to solve practical problems and deal with a variety of concrete variables in situations where only limited standardization exists. Ability to interpret a variety of instructions furnished in written, oral, diagram, or schedule form.
• Math Ability Ability to add, subtract, multiply, and divide in all units of measure, using whole numbers, common fractions, and decimals. Ability to compute rate, ratio, and percent and to draw and interpret bar graphs.
• Physical Demands - While performing the duties of this job the employee may be exposed to moving mechanical parts. The employee may be occasionally exposed to caustic chemicals and risk of electrical shock. The noise level in the environment is low to moderate.
• Computer Skills Knowledge or and previous experience using MS Office Software, Electronic Document Management Systems, E-mail is required
• Equipment Use Knowledge of and experience using equipment is required. - (Examples of equipment include Office Equipment, Biosafety Cabinets, Incubators, Single Use Bioreactors, Chromatography columns/skids, Ultrafiltration systems, drug substance filling operations, Peristaltic Pumps and Other Single Use pumps.)

Nice To Haves

• Downstream/Purification operations preferred

Responsibilities

• Generation of batch records, solution records, equipment preparation records, processing assembly records, test sampling plans and process flow charts for specific manufacturing process units.
• Manufacturing laboratory equipment: work order initiation and follow up, assessments to support deviations, troubleshooting and vendor coordination.
• CAPA and Change Control implementations, Safety Improvement implementations.
• Manufacturing operation support and troubleshooting.
• Support activities associated with Operational Excellence Initiatives including Error Proofing, Standardization, 5S, Lean Manufacturing

Benefits

• KBI has a robust total rewards strategy which includes an annual bonus structure for all employees, medical, dental, and vision coverage, paid PTO and holidays, 401K matching, and employee recognition programs.

What This Job Offers

• Job Type: Full-time
• Career Level: Entry Level
• Education Level: High school or GED
• Number of Employees: 1,001-5,000 employees