Website TalentBurst, Inc.
TalentBurst, Inc.
Company : TalentBurst, Inc.
Title: Quality Control Analyst III
Location: Norton, MA
Duration: 7+ Months
Overview
The Quality Control Operations (QCO) Analyst III Contractor plays a crucial role in supporting the department’s efforts to maintain the highest standards of quality and compliance from development through to commercialization. In addition to executing routine and non-routine testing in support of development through commercial programs, the Analyst III will also participate in data trending, investigations, and laboratory operations. This position will also play a role in method transfers, method qualification/validation, verification, and implementation. By ensuring these critical activities are executed with precision, the Analyst III significantly contributes to routine laboratory operations, thereby enhancing the overall efficiency and effectiveness of the QC functions.
This position is onsite and will be primarily located in Norton, MA, with potential occasional responsibilities at other Alnylam locations. The role requires flexibility for weekend coverage to support a continuous operational schedule. This is a first shift position Friday-Monday (4 x 10 hours), but will require an initial period of Monday-Friday work to accommodate training.
Key Responsibilities (including but not limited to):
• Perform routine and non-routine analytical and/or microbiological assays to support raw materials, in-process samples, product release, and stability studies, following established SOPs
• Support a continuous operational schedule by supporting weekend laboratory operations (Analytical, Microbiology, Raw Materials).
• Maintain up-to-date training records, adhere to the testing schedule, and ensure the timely completion of all assignments to support the seamless operation of QC activities and uphold the department’s commitment to meeting project timelines and quality metrics
• Assist in the maintenance of laboratory equipment and inventory, including the preparation of reagents and samples to ensure smooth laboratory operations
• Ensure data are reviewed timely; qualify as a data reviewer to ensure timely and efficient data availability.
• Perform role-specific operational assignments (e.g., raw material processes including SAP transactions, environmental monitoring, in-process testing, etc.).
• Contribute to the revision and updating of controlled documents, including SOPs, work instructions, and test methods, to ensure continuous improvement and compliance with current industry standards and regulatory requirements
• Adhere to internal standards, policies, and SOPs, as well as regulatory and industry standards (e.g., GMP, GLP, ICH guidelines) to maintain the highest levels of quality and compliance.
• Actively participate in continuous improvement efforts by identifying and suggesting enhancements to methods and laboratory processes, particularly those related to efficiency and reliability.
• Collaborate with QC and cross-functional teams to ensure seamless quality control operations and to support the collective Alnylam goals
• Pursue ongoing training and development to deepen expertise in QC testing techniques, TOQ operations, and regulatory compliance.
• May assist in preparing technical documentation for regulatory submissions by performing data verification, ensuring accuracy and compliance with regulatory standards.
• Participate in inspection readiness activities as well as supporting onsite audits and inspections, as needed.
• Actively participate in continuous improvement initiatives aimed at enhancing QC processes and procedures, increasing laboratory efficiency and effectiveness.
• Collaborate with other organizational functions including CMC Development, Manufacturing, Manufacturing Technical Services, Materials Management, and Quality Assurance to ensure alignment with overall business goals.
Qualifications
• B.S. in chemistry, biology, or biochemistry, or related scientific field;
• Pharmaceutical/Biotech industry experience with 4 years in a GMP Quality Control function or equivalent, relevant industry experience
• Experience in method transfer and/or analytical method implementation; solid understanding of method lifecycle management and phase-appropriate approach is desirable
• Demonstrated technical writing skills, with preference for technical writing of investigations
• Proficient in data analysis and interpretation, with excellent attention to detail to inform decision-making
• Solid problem-solving skills and experience in conducting investigations and implementing CAPA
• Strong organizational skills with the ability to manage multiple tasks simultaneously and autonomously
• Excellent communication and teamwork abilities, capable of working effectively in a collaborative environment
• Proficiency in LabWare LIMS, Excel, Word, and PowerPoint preferred
Weekend shift
Fri-Monday (8a-6p)
Full time – on site position
Extension of day to day operations
Activities GMP quality control lab and microbiology lab
Both types of labs
Not looking for both experience
Either chemistry or microbiology
Working for a GMP quality control lab
Not research end – laboratory practices needed
A couple of years – so they can get up and running
Chemistry HPLC or UPLC
Microbiology side – looking for bioburden, endotoxin,
Focus on QC Chemistry or QC Microbiology
From the manager –
From the first batch, I liked the candidates who have solid experience in GMP QC labs. There were a couple that only reviewed data or were more in research environments. Really looking for folks who are actively working in QC labs right now.
How many years of overall experience working in lab and in GMP QC lab is required? It’s a minimum of 4 years in a GMP laboratory
How many years of experience in method transfer and/or analytical method implementation, method lifecycle management is required? This would be rolled into the minimum 4 years of experience. The critical experience that I am looking for is the 4 years of experience in GMP laboratories. Of particular importance is that the experience is either in a QC Chemistry lab or QC Microbiology lab. For Chemistry, I am looking for folks with experience with HPLC/UPLC with Empower software. For Microbiology, it would be the standard suite of micro testing including Bioburden, endotoxin, conductivity, TOC (some or all).
How many years of experience would make a candidate over qualified? Over 10 years is probably too much for this role.