Remote Senior Quality Control Chemist

Placements24; Mossel Bay; Hybrid; ZAR 750,000 - 1,200,000; Full time

Benefits offered by this job

Fully remote work

Competitive salary

Health insurance

Retirement fund contributions

Professional training

Conference attendance

Paid time off

Job summary

Placements24 in South Africa seeks a Remote Senior Quality Control Chemist to safeguard the quality of raw materials, intermediates and finished goods through rigorous analytical testing. The ideal candidate holds a Master’s degree or Ph.D.

in Chemistry, 5+ years in QC/analytical chemistry, and hands-on with HPLC, GC, MS, UV-Vis, FTIR and AAS, plus GMP/GLP knowledge. This role is fully remote and offers substantial professional autonomy.

Qualifications

• Master's or PhD in Chemistry or related field.
• Minimum 5 years in QC/analytical chemistry in chemical/pharma industry.
• Experience with GMP/GLP and ISO 9001 quality systems.
• Proficient in method development and validation; strong documentation.

Responsibilities

• Perform analytical tests on raw materials, intermediates and finished goods.
• Develop, validate, and implement new analytical methods.
• Analyze results, investigate deviations and root causes.
• Maintain calibration and maintenance logs for instruments.
• Ensure compliance with GLP and regulatory requirements.
• Prepare CoA and quality documentation; participate in audits.
• Collaborate with R&D, production, and regulatory teams.
• Mentor junior staff and stay updated on analytical techniques.

Skills

HPLC

GC

MS

UV-Vis

FTIR

AAS

Education

Master's degree in Chemistry

PhD in Chemistry

Tools

HPLC

GC

MS

UV-Vis

FTIR

AAS

Job description

About the Role

Our client, a prominent innovator in the specialty chemicals sector, is seeking an experienced and meticulous Remote Senior Quality Control Chemist to join their expanding operations. This is a fully remote position, offering the flexibility to work from your home office. The role is vital in ensuring the consistent quality and integrity of raw materials, in-process samples, and finished products through rigorous analytical testing and method development. The ideal candidate will possess a deep understanding of analytical chemistry techniques, quality control systems, and regulatory compliance within the chemical industry. You will contribute to maintaining our high standards of product excellence and support our commitment to innovation. This position requires a self-starter with excellent analytical and problem-solving skills, capable of working independently in a remote setting.

Key Responsibilities

• Perform a wide range of analytical tests on raw materials, intermediate products, and finished goods using various instrumental and wet chemistry techniques.
• Develop, validate, and implement new analytical methods in accordance with relevant standards and regulatory requirements.
• Analyze test results, identify deviations from specifications, and investigate the root causes of any quality issues.
• Maintain accurate and detailed laboratory records, including instrument calibration and maintenance logs.
• Ensure compliance with Good Laboratory Practices (GLP) and relevant industry regulations.
• Collaborate with R&D, production, and regulatory affairs teams to resolve quality-related issues.
• Prepare Certificates of Analysis (CoA) and other quality-related documentation.
• Participate in internal and external quality audits.
• Stay current with advancements in analytical chemistry and quality control methodologies.
• Mentor and guide junior laboratory personnel as needed.

Requirements

• Master's degree or Ph.D. in Chemistry, Analytical Chemistry, or a related scientific discipline.
• Minimum of 5 years of experience in quality control or analytical chemistry within the chemical or pharmaceutical industry.
• Extensive experience with analytical instrumentation such as HPLC, GC, MS, UV-Vis, FTIR, and atomic absorption spectroscopy.
• Proficiency in method development and validation.
• Strong understanding of quality management systems (e.g., ISO 9001) and GMP/GLP principles.
• Excellent analytical, critical thinking, and problem-solving skills.
• Exceptional written and verbal communication skills, with the ability to document findings clearly and concisely.
• Proven ability to work independently, manage time effectively, and meet deadlines in a remote environment.
• Familiarity with relevant industry regulations and pharmacopeias.
• Strong attention to detail and commitment to accuracy.

Benefits

• This fully remote role offers the ultimate flexibility and the chance to work from any location.
• Our client provides a highly competitive salary, comprehensive health insurance, and a substantial contribution to a retirement fund.
• Significant opportunities for professional growth through advanced training, workshops, and conference attendance are available.
• You will be part of a research-driven organization that values scientific rigor and innovation.
• Access to cutting-edge analytical tools and resources.
• A collaborative virtual team environment that fosters knowledge sharing.
• Generous paid time off and standard public holidays.
• The company is committed to employee well-being and offers resources to support a healthy lifestyle.