Remote Quality Control Specialist - Pharmaceutical

Placements24; Stellenbosch Local Municipality; Remote; ZAR 500,000 - 700,000; Full time

Benefits offered by this job

Health insurance

Retirement plan

Job summary

Placements24 invites applications for a fully remote Quality Control Specialist role with a globally recognized pharmaceutical company. You will review QC data, ensure GMP/ICH compliance, and support regulatory audits from home.

Ideal candidates hold a science degree and have QC/QA experience in pharma, strong data analysis, and proficiency with ELNs and LIMS. This position emphasizes independent work and remote collaboration.

Qualifications

• Bachelor's degree in Pharmacy, Chemistry, Biology, or related life science field.
• Proven experience in quality control or quality assurance within pharmaceutical/biopharmaceutical industry.
• In-depth knowledge of GMP, ICH guidelines, and regulatory requirements for pharmaceuticals.
• Strong analytical skills with the ability to interpret complex data.
• Proficiency in ELNs, LIMS, and quality management software.

Responsibilities

• Review and analyze quality control data from manufacturing batches.
• Ensure QC activities comply with cGMP and FDA guidelines.
• Prepare and maintain certificates of analysis, test results, and batch records.
• Identify deviations and participate in root-cause investigations.
• Collaborate with R&D, Manufacturing, Regulatory Affairs remotely.

Skills

Analytical skills

Attention to detail

Self-motivated

Remote collaboration

Organizational skills

Communication skills

Education

Bachelor's degree in Pharmacy, Chemistry, Biology, or related life science field

Tools

ELNs

LIMS

Quality management software

Job description

About the Role

Our client, a globally recognized pharmaceutical company, is seeking a dedicated and detail-oriented Remote Quality Control Specialist. This position is fully remote, allowing you to contribute to our client's mission of delivering high-quality pharmaceutical products from the comfort of your home. The specialist will be responsible for reviewing and analyzing quality control data, ensuring compliance with strict regulatory standards (e.g., GMP, FDA guidelines), and participating in quality improvement initiatives. This role requires a meticulous approach to data management, a strong understanding of pharmaceutical quality systems, and excellent analytical skills. You will be an essential part of our client's commitment to excellence, working remotely to uphold the integrity of their pharmaceutical products. This role is designed for a self-motivated individual who thrives in an independent work environment.

Key Responsibilities

• Review and analyze quality control data from various manufacturing batches and processes.
• Ensure all quality control activities comply with current Good Manufacturing Practices (cGMP), FDA regulations, and other relevant pharmaceutical guidelines.
• Prepare and maintain accurate documentation, including certificates of analysis, test results, and batch records.
• Identify deviations from quality standards and participate in investigations to determine root causes and implement corrective actions.
• Collaborate with internal teams (e.g., R&D, Manufacturing, Regulatory Affairs) via virtual channels to resolve quality-related issues.
• Assist in the preparation for and participation in regulatory audits and inspections.
• Contribute to the continuous improvement of quality control processes and systems.
• Stay up-to-date with relevant pharmaceutical regulations and quality best practices.
• Manage and maintain electronic quality management systems and databases.
• Provide support for product release activities by ensuring all quality requirements are met.

Requirements

• Bachelor's degree in Pharmacy, Chemistry, Biology, or a related life science field.
• Proven experience in quality control or quality assurance within the pharmaceutical or biopharmaceutical industry.
• In-depth knowledge of GMP, ICH guidelines, and regulatory requirements for pharmaceuticals.
• Strong analytical skills with the ability to interpret complex data.
• Proficiency in using electronic laboratory notebooks (ELNs), LIMS (Laboratory Information Management Systems), and other quality management software.
• Excellent attention to detail and organizational skills.
• Strong written and verbal communication skills, essential for remote collaboration.
• Self-motivated and able to work independently with minimal supervision.
• Demonstrated ability to manage multiple tasks and meet deadlines in a remote setting.

Benefits

Our client offers a competitive salary and comprehensive benefits package, including health insurance and retirement plan options. This fully remote role provides flexibility and the opportunity to work with a leading pharmaceutical company without the need for commuting. Enjoy the advantages of a flexible work environment while making a significant contribution to pharmaceutical quality.