Quality Control Analyst - Pharmaceutical Manufacturing

Placements24

Queenstown

Vor Ort

NZD 46.000 - 59.000

Vollzeit

Vor 6 Tagen
Sei unter den ersten Bewerbenden

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Benefits dieser Stelle

Medical aid benefits
Provident fund participation
On-the-job training and development
Annual leave and sick leave

Zusammenfassung

Placements24 is seeking a Quality Control Analyst for our pharmaceutical client in Queenstown (Eastern Cape). You will perform routine analytical testing of raw materials, in-process samples and finished products using HPLC, GC and UV-Vis spectroscopy, ensuring GMP compliance and high data integrity.

You will calibrate instruments, review results, and participate in method validation and OOS investigations while maintaining meticulous records and a safe lab environment.

Qualifikationen

  • Bachelor's degree in Chemistry, Pharmacy, Biotechnology, or related field.
  • Minimum 2 years of Quality Control lab experience.
  • Proficiency with HPLC, GC, UV-Vis and wet chemistry.
  • GMP familiarity and regulatory knowledge.
  • Experience with LIMS desirable.

Aufgaben

  • Perform routine analytical testing of raw materials, intermediates and finished products using HPLC, GC, UV-Vis and titrations.
  • Conduct stability testing and environmental monitoring per protocols.
  • Prepare reagents, standards and solutions for analyses.
  • Calibrate and maintain laboratory equipment and track calibration schedules.
  • Document all activities and results in GMP-compliant systems.
  • Investigate OOS results and assist with root cause analysis.
  • Assist in validation/verification of methods and equipment.
  • Review data to ensure products meet specifications.
  • Maintain a clean, organized and safe laboratory.
  • Comply with health, safety and environmental regulations.

Kenntnisse

HPLC
GC
UV-Vis spectroscopy
Wet chemistry
Data accuracy
Independent & team work

Ausbildung

Bachelor's degree in Chemistry, Pharmacy, Biotechnology, or related

Tools

LIMS

Jobbeschreibung

About the Role

Our client, a reputable pharmaceutical manufacturer, is looking for a dedicated Quality Control Analyst to join their laboratory team in Queenstown, Eastern Cape. This role is essential for ensuring the quality and safety of pharmaceutical products through rigorous testing and analysis of raw materials, in-process samples, and finished goods. The successful candidate will perform a variety of analytical tests using sophisticated laboratory equipment and adhere strictly to Good Manufacturing Practices (GMP) and standard operating procedures. This is a hands-on laboratory role requiring meticulous attention to detail and a commitment to upholding the highest quality standards. Working in Queenstown, Eastern Cape, offers a unique community setting with opportunities to contribute to local industry growth. The position is crucial for maintaining product integrity and patient safety within the pharmaceutical supply chain. This is a vital role within the manufacturing process, ensuring every product meets stringent specifications.

Key Responsibilities
  • Perform routine analytical testing on raw materials, intermediates, and finished pharmaceutical products using techniques such as HPLC, GC, UV-Vis spectroscopy, and titrations.
  • Conduct stability testing and environmental monitoring according to established protocols.
  • Prepare reagents, solutions, and standards required for analytical testing.
  • Calibrate and maintain laboratory equipment, ensuring proper functioning and adherence to calibration schedules.
  • Document all laboratory activities, test results, and observations accurately and meticulously in compliance with GMP and company SOPs.
  • Investigate Out-of-Specification (OOS) results and participate in root cause analysis.
  • Assist in the validation and verification of analytical methods and equipment.
  • Review and interpret analytical data to ensure products meet quality specifications.
  • Maintain a clean and organized laboratory environment.
  • Ensure compliance with all health, safety, and environmental regulations.
Requirements
  • Bachelor's degree in Chemistry, Pharmacy, Biotechnology, or a related scientific discipline.
  • Minimum of 2 years of experience in a Quality Control laboratory, preferably within the pharmaceutical industry.
  • Proficiency in performing common analytical techniques such as HPLC, GC, and wet chemistry.
  • Familiarity with Good Manufacturing Practices (GMP) and regulatory requirements.
  • Experience with laboratory information management systems (LIMS) is desirable.
  • Strong attention to detail and accuracy in data recording and analysis.
  • Good organizational and time management skills.
  • Ability to work independently and as part of a team.
  • Basic understanding of instrument calibration and maintenance.
  • Good written and verbal communication skills in English.
Benefits
  • Our client offers a competitive salary, medical aid benefits, and participation in a provident fund.
  • Opportunities for on-the-job training and development in analytical techniques are provided.
  • A stable and supportive work environment is guaranteed.
  • Paid time off includes annual leave and sick leave.
  • The role is situated in Queenstown, Eastern Cape, offering a quieter pace of life while contributing to an essential industry.
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