Remote Pharmaceutical Quality Control Specialist

Darum lohnt es sich

Key Responsibilities • Develop, validate, and implement quality control testing procedures for raw materials, intermediates, and finished pharmaceutical products. • Perform analytical testing using various laboratory instruments and techniques, such as HPLC, GC, and spectroscopy. • Review and approve batch records, ensuring compliance with established specifications and Good Manufacturing Practices (GMP). • Investigate deviations and out-of-specification (OOS) results, documenting findings and recommending corrective and preventive actions (CAPA). • Maintain detailed records of all quality control activities, ensuring traceability and audit readiness. • Collaborate with manufacturing, R&D, and regulatory affairs teams to resolve quality-related issues.

Benefits • Competitive annual compensation package. • Fully remote work environment with flexible hours. • Comprehensive health, dental, and vision benefits. • Paid time off and opportunities for professional development. • A supportive and collaborative team culture focused on maintaining the highest quality standards.

About the Role Our client seeks a dedicated and experienced Remote Pharmaceutical Quality Control Specialist to bolster their quality assurance efforts, operating entirely from home to serve operations based in Rustenburg .

This critical role ensures that all pharmaceutical products meet stringent quality standards and regulatory requirements through meticulous testing and documentation.

You will play a key part in maintaining the integrity and safety of our client's pharmaceutical offerings by performing detailed analyses and implementing robust quality control procedures. This is an exceptional opportunity for a quality professional looking for a remote role within the vital pharmaceutical sector.

Requirements • Bachelor's degree in Chemistry, Pharmacy, Biotechnology, or a related scientific field. • Minimum of 3 years of experience in pharmaceutical Quality Control (QC) or Quality Assurance (QA). • Strong knowledge of GMP, FDA, and other relevant regulatory guidelines. • Proficiency with analytical instrumentation and laboratory techniques common in the pharmaceutical industry. • Excellent attention to detail, organizational skills, and the ability to manage multiple tasks effectively. • Strong written and verbal communication skills for reporting and cross-functional collaboration.