Senior Pharmaceutical QC Analyst | Growth, Training & Benefits

Placements24

Pietermaritzburg

Ibrido

ZAR 600.000 - 900.000

Tempo pieno

3 giorni fa
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Curriculum e lettera di presentazione personalizzati, pronti da inviare.

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Vantaggi offerti da questo lavoro

Competitive remuneration package
Medical aid plan
Retirement fund
Performance-based bonuses
Training and development opportunities
Career advancement opportunities

Descrizione del lavoro

Placements24 is seeking a highly skilled Senior Pharmaceutical Quality Control Analyst to join the team in Pietermaritzburg. The role focuses on analytical testing across raw materials, in-process samples, and finished products to ensure regulatory compliance and product quality.

You will develop and validate analytical methods, investigate OOS results, and maintain GLP/GMP-compliant records while collaborating with R&D, Manufacturing, and Regulatory Affairs to support the product lifecycle.

Competenze

  • Bachelor's or Master's degree in Pharmacy, Chemistry, or a related scientific discipline.
  • Minimum of 5 years of progressive experience in pharmaceutical quality control or quality assurance.
  • Proven expertise in operating and maintaining analytical instruments such as HPLC, GC, dissolution testers, and spectrophotometers.
  • Thorough understanding of pharmaceutical regulatory requirements (SAHPRA, ICH, GMP, GLP).
  • Experience in method development and validation is highly desirable.
  • Strong analytical and problem-solving skills, with a proven ability to investigate and resolve complex technical issues.
  • Excellent written and verbal communication skills, with the ability to clearly document findings and present technical information.
  • Proficiency in data analysis and interpretation, with a meticulous approach to record-keeping.
  • Familiarity with LIMS is a plus.

Mansioni

  • Perform analytical tests on raw materials, in-process samples, and finished pharmaceutical products using analytical instrumentation (e.g., HPLC, GC, UV-Vis, FTIR).
  • Develop, validate, and transfer analytical methods in accordance with regulatory guidelines (e.g., ICH, FDA, SAHPRA).
  • Investigate out-of-specification (OOS) results, identify root causes, and implement CAPAs.
  • Maintain accurate and detailed laboratory records, ensuring compliance with GLP and GMP.
  • Prepare and review analytical reports, certificates of analysis (CoAs), and other quality documentation.
  • Calibrate and maintain laboratory equipment, ensuring its optimal performance and accuracy.
  • Collaborate with cross-functional teams, including R&D, Manufacturing, and Regulatory Affairs, to resolve quality issues and support product lifecycle management.
  • Stay updated with the latest scientific advancements, regulatory changes, and industry best practices in pharmaceutical quality control.
  • Mentor and train junior analysts, fostering a culture of continuous improvement and knowledge sharing within the QC department.

Conoscenze

Analytical chemistry
Problem solving
Data analysis
Independent worker
Team collaboration

Formazione

Bachelor's or Master's in Pharmacy or Chemistry

Strumenti

LIMS

Descrizione del lavoro

Placements24 is seeking a highly skilled Senior Pharmaceutical Quality Control Analyst to join the team in Pietermaritzburg. The role focuses on analytical testing across raw materials, in-process samples, and finished products to ensure regulatory compliance and product quality.

You will develop and validate analytical methods, investigate OOS results, and maintain GLP/GMP-compliant records while collaborating with R&D, Manufacturing, and Regulatory Affairs to support the product lifecycle.

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