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Manufacturing Compliance Specialist

Job in Durham, Durham County, North Carolina, 27703, USA
Listing for: KBI Biopharma
Full Time position
Listed on 2026-01-02
Job specializations:
  • Quality Assurance - QA/QC
  • Healthcare
Job Description & How to Apply Below

Job Summary

The Manufacturing Compliance Specialist supports the rapidly expanding GMP Contract Manufacturing Operation. The Specialist will need to produce high-quality documentation that contributes to the overall success of our operations. Independently responsible for the efficient and thorough investigation of process deviations (that occur in manufacturing; Upstream, Downstream and/or Support), determination of root cause, and initiation of corrective/preventative actions designed to adequately address and correct the Quality related deficiencies identified during the investigation process.

Responsible to provide proactive corrections based on noted trends to minimize the potential for repeat incidents. The position requires working with minimal supervision to manage assigned investigations from initiation to completion. The Specialist should have some experience in biotechnology manufacturing and quality system writing.

Job Responsibilities
  • As part of each investigation, gathers information from all necessary internal and external sources in order to evaluate the impact of the deviation on manufactured product, as well as the risk to future operations.
  • The Specialist will conduct and drive closure of non-conformance events to identify root cause, product impact and preventative actions for Manufacturing Operations in support of batch disposition and continuous process improvement. Work with internal teams to obtain an in-depth understanding of the product and the documentation requirements.
  • Properly assess the manufacturing or analytical environment and independently conceives and documents appropriate corrective/preventative actions designed to mitigate Quality deficiencies identified in the investigative process using analytical tools.
  • Analyze existing deviations and a potential deviation focusing on establishes effective corrective and preventive actions to minimize the reoccurrence of the event.
  • Produce high-quality documentation that meets applicable standards and is appropriate for its intended audience.
  • Complete investigations and CAPAs in alignment with established procedures and timelines.
  • Work across functions with a professional manner to conduct investigations and CAPAs.
  • Works independently to comply with procedure driven guidelines relating to Deviation investigations and CAPAs.
  • Demonstrates strong technical skills. Provides technical assistance to area supervisors or managers to solve complex problems. Exercises judgment in developing practices, techniques and evaluation criteria for obtaining results.
  • Assist immediate manager with achieving departmental requirements by meeting or exceeding productivity, quality and capacity objectives.
  • Gathers information from all necessary internal and external sources in order to evaluate the impact of the deviation on manufactured product, as well as the risk to future operations.
  • Analyze existing and potential content, focusing on reuse and single-sourcing opportunities.
  • Produce high-quality documentation that meets applicable standards and is appropriate for its intended audience.
  • Demonstrates strong technical skills.
  • Provides technical assistance to area supervisors or managers to solve complex problems.
  • Exercises judgment in developing practices, techniques and evaluation criteria for obtaining results.
  • Work off-shift hours as necessary or assigned.
Requirements Knowledge, Skills, Abilities
  • BA/BS Degree in science field, e.g., Biology, Microbiology, Chemistry, Pharmacy, etc. or equivalent combination of education and experience.
  • 3-5 years of pharmaceutical or related work experience with emphasis on current Good Manufacturing Practices including: QA, QC, Validation, Manufacturing, or process engineering.
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 reports and correspondence.
  • Ability to speak effectively before internal groups or employees of organization.
  • Good deductive and inductive critical thinking skills required.
Reasoning Ability
  • Ability to solve practical problems and deal with a variety of…
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