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Senior Manufacturing Specialist

KBI Biopharma

Durham, NCOnsitePosted 35 days ago
Full TimeSenior LevelManufacturing & CMCCDMO
Original posting ↗

Summary

Responsible for leading technical support activities for GMP Manufacturing Operations in a multi-product, large scale, biopharmaceutical facility.

Job description

Job Responsibilities

  • New Product/Process Introduction and Changes including: Facility Fit support, Manufacturing Record and procedure drafting, Equipment procurement or modification, Training generation
  • Drafting, routing, and revision of manufacturing batch records, procedures, supporting records.
  • Serve as technical SME in manufacturing operations, coaching and mentoring manufacturing associates, supporting trainers in development of TRNs
  • Manufacturing process support during on-going shop floor execution.
  • Engage with Manufacturing Associates and Supervisors to understand barriers to success, identify opportunities for improvement. Drive and manage projects with significant process improvement impact
  • Lead implementations for corrective and preventive actions. Partner with Compliance/QA for timely Deviation Investigation completion
  • Support activities associated with Operational Excellence Initiatives including: Error Proofing, Standardization, 5S, Lean Manufacturing
  • Support safety initiatives, compliance & quality requirements.

Knowledge, Skills, Abilities

  • Demonstrated knowledge of downstream operations is preferred, cell culture and/or fermentation
  • Experience in single-use platform technology is preferred
  • Bachelor's degree in a related scientific or engineering discipline preferred with 6+ year's related experience and/or training; or equivalent experience
  • Requires minimal direction or supervision to execute against routine tasks.
  • Fluent in English with excellent written and verbal communication skills are required.
  • Must be detail oriented, have good time management skills and be customer focused
  • Must be organized and able to focus in a face-paced, multi-tasked environment and maintain operational efficiency and positive demeanor.

Working Conditions

The job requires supporting a 24-hour manufacturing facility which may include on call phone support or support overnight and on weekends. The job requires working within a cGMP manufacturing biotechnology facility which requires clean room operations. Clean room operations require donning clean room attire when entering clean room areas and maintaining good personal hygiene. While performing the duties of this job the employee may use equipment and materials which include mechanical hazards, chemical hazards, electrical hazards, and tripping and falling hazards. The noise level in the manufacturing environment is moderate to high, however, employee will routinely work in office area.

Requirements

  • Bachelor's degree in a related scientific or engineering discipline preferred
  • 6+ years related experience and/or training; or equivalent experience
  • Demonstrated knowledge of downstream operations is preferred, cell culture and/or fermentation
  • Experience in single-use platform technology is preferred
  • Fluent in English with excellent written and verbal communication skills are required
  • Must be detail oriented, have good time management skills and be customer focused
  • Must be organized and able to focus in a face-paced, multi-tasked environment and maintain operational efficiency and positive demeanor
  • Requires minimal direction or supervision to execute against routine tasks

Company overview

KBI Biopharma is an award-winning global contract development and manufacturing organization (CDMO) that provides fully integrated, accelerated drug development and biologics manufacturing services to pharmaceutical and biotechnology companies worldwide. Founded in 1996 and now part of JSR Life Sciences, KBI has established itself as a next-generation CDMO specializing in complex biologics. The company serves over 500 client partners and has supported the advancement of more than 160 drug candidates from preclinical stages to market, including the manufacture of ten commercial products. KBI's comprehensive service portfolio includes cell line development, process development, analytical services, formulation development, and clinical and commercial cGMP manufacturing for both mammalian and microbial programs. With strategically located facilities across the United States and Europe, KBI leverages world-class analytical capabilities and proprietary platforms like SUREtechnology™ and PUREplatform™ to deliver personalized, accelerated solutions for biopharmaceutical development. The company is recognized for its scientific excellence, quality manufacturing, and commitment to helping clients bring innovative medicines to patients faster.

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