Quality Control Lab Technician I
Curia
Summary
The principal responsibility of Quality Control Lab Technician I is the analysis by multiple procedures of intermediates and target compounds. This role is expected to demonstrate expertise in both the theoretical and practical aspects of analytical chemistry. In general, the Quality Control Lab Technician I provides technical, organizational and compliance support for 170+ ongoing stability studies.
Job description
Responsibilities
- Perform microbiological testing (endotoxin, bioburden) for water
- Perform microbiological testing (endotoxin, sterility and bioburden) for raw materials, in-process materials, intermediates and final product
- Perform environmental monitoring of the clean rooms (under USP and EU specifications)
- Review documentation, analytical chromatographic data and results from instrumental testing such as DSC, XRPD, water analysis, USP testing, etc. for compliance with cGMPs, Curia SOPs and other written procedures
- Analyze data for stability trends and deviations to ensure consistency with historical time points and prevent unexpected results
- Manage timelines and multiple projects by interfacing with scientists and management to coordinate testing timelines, corrections to documentation, and reporting within defined turnaround times
- Adjust priorities based on due dates and invoicing goals
- Assist in writing stability protocols
- Interact with outside testing laboratories to coordinate shipment and testing of stability samples
- Develop direct, technical communication with primarily external customers to report results, engage in technical discussion and address questions
- Review and format reports such as Stability Summary tables to ensure accuracy and compliance with current Curia formats
- Manage invoicing for stability, which includes issuing BRFs, working with finance to ensure accurate and complete accounting for stability projects, reviewing monthly invoices and tracking monthly and quarterly financial projections
- Handle controlled substances including maintaining inventory, completing paperwork, and conducting biannual review
- Manage workload and time to enable the incumbent to perform multiple projects effectively and ensure all necessary paperwork is completed on a timely basis
- Volunteer to assist with other tasks in the analytical function not directly related to specific projects
- Participate in self-development activities and training others
- Write proposals and design studies for stability
Qualifications
- High school diploma or general education degree (GED)
- Minimum 0-1 years' relevant experience in a pharmaceutical testing laboratory
- Preferred Bachelor's degree in chemistry, biology or related science
- Must pass a background check
- Must pass a drug screen
- May be required to pass Occupational Health Screening
Requirements
- High school diploma or general education degree (GED)
- Minimum 0-1 years' relevant experience in a pharmaceutical testing laboratory
- Preferred Bachelor's degree in chemistry, biology or related science
- Must pass a background check
- Must pass a drug screen
- May be required to pass Occupational Health Screening
Benefits
- Generous benefit options
- Paid training
- Paid vacation
- Paid holidays
- Career advancement opportunities
- Education reimbursement
- 401(k) Matching
- Learning platform
Company overview
Curia is a leading global Contract Development and Manufacturing Organization (CDMO) with over 30 years of experience in the pharmaceutical industry. Headquartered in Albany, New York, the company operates an integrated network of 25 global sites across North America, Europe, and Asia, employing approximately 3,500 professionals. Curia provides comprehensive end-to-end solutions spanning drug discovery, development, and manufacturing services for both small molecules and biologics. Their expertise covers active pharmaceutical ingredient (API) manufacturing, sterile drug product development, analytical testing, and regulatory support. The company specializes in complex areas including high-potency compounds, controlled substances, sterile APIs, and mRNA manufacturing. With state-of-the-art GMP facilities and a strong focus on innovation, Curia partners with pharmaceutical and biotechnology companies to accelerate the development and commercialization of life-changing therapeutics, from early-stage discovery through commercial-scale production.