Job summary
Job post source
This job is directly from Pharmaron
Job overview
The GMP QC Analyst I/II at Pharmaron supports the Cell & Gene Therapy Quality Control team by performing routine laboratory testing under cGMP conditions to ensure quality and regulatory compliance for client projects.
Responsibilities and impact
The role involves performing analytical testing including ELISA, qPCR, ddPCR, cell culture, cell line banking, method validation, instrument maintenance, documentation, and collaboration with QA and R&D teams to support quality control and compliance.
Compensation and benefits
The position offers a salary range of $65,000 to $70,000 per year, comprehensive medical, dental, and vision insurance with employer contributions, employer-funded health reimbursement account, flexible spending accounts, fully employer-paid life and disability insurance, a 401k plan with employer match, and access to an employee assistance program.
Experience and skills
Candidates should have a degree in biological sciences or related fields, with 1-5 years of experience depending on level (I or II), knowledge of aseptic technique, cell culture, molecular biology methods, and strong data recording skills.
Career development
Pharmaron offers opportunities to gain hands-on experience in a dynamic, client-focused environment with potential growth in the CGT laboratory and cross-functional collaboration.
Work environment and culture
Pharmaron promotes an inclusive, collaborative culture valuing teamwork, innovation, and employee and client focus, emphasizing diversity and inclusion.
Company information
Pharmaron is a premier life sciences R&D service provider founded in 2004, with over 19,000 employees and operations in the U.S., U.K., and China, delivering broad drug discovery and development services across multiple therapeutic modalities.
Team overview
The candidate will join the Cell & Gene Therapy Quality Control team, working cross-functionally with QA, R&D, and other departments in a collaborative environment.
Job location and travel
The position is located on-site in Exton, Pennsylvania, with no mention of remote work or travel requirements.
Application process
Applicants are instructed to apply online through Pharmaron's website and are encouraged to join a diverse and inclusive workplace.
Unique job features
The job offers unique exposure to cutting-edge CGT laboratory techniques and client-specific method validation in a regulated cGMP environment.
Company overview
Pharmaron is a global contract research organization (CRO) that provides comprehensive R&D services to the pharmaceutical and biotech industries. They generate revenue by offering services across the drug discovery, preclinical, and clinical development stages, including chemistry, biology, pharmacology, and manufacturing. Founded in 2004 in Beijing, Pharmaron has expanded its operations worldwide, establishing a significant presence in the U.S., U.K., and China. Key historical milestones include its IPO on the Shenzhen Stock Exchange in 2019 and strategic acquisitions to enhance its service capabilities.
How to land this job
Tailor your resume to highlight hands-on experience with GMP-regulated laboratory testing, focusing on biological assays like ELISA, qPCR, ddPCR, and cell-based potency assays, as these are core to the GMP QC Analyst role at Pharmaron.
Emphasize your familiarity with aseptic cell culture techniques, cell line banking, and method validation activities, showcasing your ability to maintain compliance with cGMP and data integrity standards such as ALCOA+.
Apply through multiple platforms including Pharmaron’s official corporate careers page and LinkedIn to maximize your application visibility and ensure you reach recruiters through different channels.
Connect with current employees in the Cell & Gene Therapy Quality Control division on LinkedIn; start conversations by commenting on recent projects they have shared or by expressing genuine interest in Pharmaron’s innovations in CGT research and development.
Optimize your resume for ATS by incorporating keywords from the job description like 'GMP', 'biological assays', 'aseptic technique', 'cell culture', 'method validation', and 'data integrity' to pass automated screenings effectively.
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