Senior Pharmaceutical Quality Control Analyst - Remote Opportunities

Placements24; Kimberley; Hybrid; CAD 90,000 - 140,000; Full time

Benefits offered by this job

Bonus program

Health insurance

Dental & vision

Job summary

Placements24 is seeking a Senior Pharmaceutical Quality Control Analyst to join a fully remote team. You will conduct analytical testing (HPLC, GC, UV-Vis, FTIR) on raw materials and finished products, interpret results, and ensure GMP compliance from a home-based lab.

The ideal candidate holds a Bachelor’s or Master’s in Chemistry with 4+ years in pharmaceutical QC or analytical development, and is proficient with LIMS. Remote collaboration and precise data handling are essential for success.

Qualifications

• Bachelor's or Master's degree in Chemistry, Analytical Chemistry, Pharmaceutical Sciences, or a related field.
• Minimum of 4 years of experience in pharmaceutical quality control or analytical development.
• Proven experience with HPLC, GC, and other common analytical techniques.
• Strong understanding of GMP principles and regulatory requirements.
• Experience with method validation is highly desirable.

Responsibilities

• Perform analytical testing on raw materials, in-process samples, and finished products using instrumental techniques (HPLC, GC, UV-Vis, FTIR).
• Analyze and interpret test results, ensuring accuracy and compliance with specifications.
• Document all laboratory activities in accordance with GMP guidelines.
• Participate in development, validation, and transfer of analytical methods.
• Operate and maintain laboratory equipment, ensuring calibration and readiness.
• Troubleshoot analytical methods and instrumentation issues.
• Prepare certificates of analysis and contribute to quality control reporting.
• Review data generated by other analysts for accuracy and completeness.
• Stay updated on regulatory guidelines and scientific literature.
• Contribute to laboratory investigations and CAPA resolutions.

Skills

Analytical testing

Data interpretation

Regulatory compliance

Remote collaboration

Education

Bachelor's degree in Chemistry

Master's degree in Chemistry

Tools

HPLC

GC

Analytical techniques

Job description

About the Role

Our client, a leading pharmaceutical company committed to the highest standards of quality, is seeking a skilled Senior Pharmaceutical Quality Control Analyst to join their fully remote team. This position offers the flexibility to work from anywhere, contributing to the critical analysis and testing of pharmaceutical products to ensure their safety, efficacy, and quality. You will perform a variety of analytical tests, interpret results, and contribute to method development and validation. The role requires a deep understanding of analytical chemistry techniques, laboratory practices, and regulatory requirements within the pharmaceutical industry. The ideal candidate is highly detail-oriented, proficient with analytical instrumentation, and capable of working independently in a virtual setting. This is an exceptional opportunity for an experienced analyst to advance their career while contributing to the development of life-changing medicines from the convenience of their home environment. Embrace a career where your analytical expertise directly impacts patient well-being.

Key Responsibilities

• Perform analytical testing on raw materials, in-process samples, and finished products using various instrumental techniques (e.g., HPLC, GC, UV-Vis, FTIR).
• Analyze and interpret test results, ensuring accuracy and compliance with specifications.
• Document all laboratory activities meticulously in accordance with GMP guidelines.
• Participate in the development, validation, and transfer of analytical methods.
• Operate and maintain laboratory equipment, ensuring calibration and readiness.
• Troubleshoot analytical methods and instrumentation issues.
• Prepare certificates of analysis and contribute to quality control reporting.
• Review data generated by other analysts for accuracy and completeness.
• Stay updated on relevant scientific literature and regulatory guidelines.
• Contribute to laboratory investigations and CAPA resolutions.

Requirements

• Bachelor's or Master's degree in Chemistry, Analytical Chemistry, Pharmaceutical Sciences, or a related field.
• Minimum of 4 years of experience in pharmaceutical quality control or analytical development.
• Proven experience with HPLC, GC, and other common analytical techniques.
• Strong understanding of GMP principles and regulatory requirements.
• Experience with method validation is highly desirable.
• Excellent data interpretation and problem-solving skills.
• Exceptional attention to detail and organizational abilities.
• Strong written and verbal communication skills, essential for remote collaboration.
• Ability to work independently and manage workload effectively in a remote setting.
• Proficiency in LIMS and electronic data management systems is a plus.

Benefits

• Competitive salary and annual bonus structure.
• Comprehensive health, dental, and vision insurance coverage.
• Generous paid time off and company holidays.
• Retirement savings plan with employer matching.
• Professional development opportunities, including training and certifications.
• Fully remote work arrangement with a home office setup stipend.
• Access to advanced digital collaboration platforms.
• Opportunity to work with a leading pharmaceutical company.
• Flexible working hours.
• A supportive and collaborative virtual team environment.