Entry-Level Qc Analyst

Overview

• Embark on a rewarding career as an Entry-Level QC Analyst in a dynamic, innovation-driven environment.
• Contribute to cutting-edge research and quality control in gene therapy applications.
• Gain hands-on experience with advanced laboratory techniques, including immunoassays and cell-based bioassays.
• Collaborate with multidisciplinary teams to ensure compliance with GMP standards.
• Enhance your technical skills through method transfer and reagent qualification activities.
• Participate in drafting and reviewing technical documents and SOPs.
• Ideal for individuals passionate about advancing their expertise in quality control.
• Work in a supportive environment that fosters professional growth and development.

Key Responsibilities & Duties

• Conduct immunoassays and cell-based assays to support product testing and stability analysis.
• Assist in drafting and reviewing SOPs and technical documentation for laboratory operations.
• Support method transfer and qualification of reagents under expert supervision.
• Maintain laboratory instruments and ensure proper calibration and upkeep.
• Collaborate with internal and external teams to achieve project goals efficiently.
• Contribute to investigations and deviation reports to uphold quality standards.
• Ensure compliance with GMP regulations in all laboratory activities.
• Review and analyze QC data to ensure accuracy and reliability.

Job Requirements

• Bachelor’s degree in Cell Biology, Molecular Biology, Biochemistry, or related field required.
• Experience with mammalian cell culture and ELISAs is preferred.
• Proficiency in basic laboratory techniques and data analysis methods essential.
• Strong organizational and communication skills are critical for success.
• Detail-oriented with a commitment to maintaining high-quality standards.
• Ability to work collaboratively within a team and independently as needed.
• Enthusiasm for learning and growing in a regulated laboratory environment.
• Dedication to upholding compliance with GMP and regulatory guidelines.