🌟 We're Hiring : Quality Control Analyst! 🌟
We are seeking a detail-oriented Quality Control Analyst to ensure our products meet the highest standards of quality and compliance. The ideal candidate will have strong analytical skills, attention to detail, and experience in quality assurance processes to maintain product excellence and customer satisfaction.
📍 Location : Norton, MA
What You'll Do :
- Perform routine and non-routine analytical assays to support raw materials, in-process samples, product release, and stability studies under supervision, following established SOPs
- 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
- Accurately record experimental data and observations in compliance with GxP standards. Participate in the review of data commensurate with experience.
- 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 goals
- Pursue ongoing training and development to deepen expertise in QC analytical techniques and regulatory compliance.
What We're Looking For :
Bachelor’s degree in Chemistry, Biochemistry, Pharmaceutical Sciences, or a related field0 to 2 years of experience in a GMP / GLP regulated laboratory environment, with exposure to pharmaceutical or biotechnology industries preferredUnderstanding of analytical techniques and their application in raw materials, in-process testing, release, and stability studies is preferredStrong documentation skills and attention to detail, with an unwavering commitment to quality and complianceBasic awareness of regulatory guidelines relevant to pharmaceutical QC (GMP, GLP, ICH) is desirableEffective communication and teamwork skills, with the ability to work collaboratively across functionsCapable of working under supervision and following detailed instructionsReady to ensure excellence? 🚀 Apply now and let's maintain quality together!