BioPharma Consulting JAD Group · 1 week ago
Quality Control Analyst II
Norton, MA
Contract
Onsite
Mid, Senior Level
4+ years expBioPharma Consulting JAD Group is focused on supporting quality control activities across development through commercial programs. The Quality Control Analyst II performs routine and non-routine analytical testing in a regulated laboratory environment, contributing to data integrity and ensuring compliance with regulatory standards.
ConsultingTherapeutics
Responsibilities
Perform routine and non-routine analytical assays of increasing complexity in support of raw materials, in-process samples, product release, and stability studies, following approved SOPs
Maintain accurate and current training records and adhere to testing schedules to ensure timely completion of assigned work
Support day-to-day laboratory operations, including equipment maintenance, reagent preparation, sample preparation, and inventory management
Ensure timely and accurate submission of analytical data; may serve as a data reviewer to support efficient data availability
Execute role-specific operational activities such as raw material sampling and testing, environmental monitoring, and product testing
Assist with method transfers, method qualification/validation, verification, and implementation activities as assigned
Contribute to the revision and maintenance of controlled documents, including SOPs, work instructions, and test methods
Adhere to internal standards, policies, and procedures, as well as regulatory and industry requirements (e.g., GMP, GLP, ICH)
Collaborate with QC and cross-functional teams to support seamless quality control operations
Participate in inspection readiness activities and support internal and external audits and inspections
Assist with data verification activities for regulatory submissions, as needed
Support continuous improvement initiatives to enhance QC processes, laboratory efficiency, and effectiveness
Collaborate with Manufacturing, Materials Management, and Quality Assurance to ensure alignment with operational and business objectives
Pursue ongoing training and development to strengthen technical expertise and regulatory knowledge
Qualification
Required
Bachelor's degree in Chemistry, Biology, Biochemistry, or a related scientific field; Associate degree, Biotech Certificate, or equivalent experience may be considered
4-8 years of experience in the pharmaceutical or biotechnology industry within a regulated Quality Control or laboratory environment
Experience performing analytical testing in compliance with GMP/GLP requirements
Ability to work under direction with strong attention to detail in a dynamic environment with shifting priorities
Strong communication and teamwork skills with the ability to collaborate effectively across functions
Preferred
Data analysis experience preferred
Familiarity with LIMS and proficiency in Microsoft Excel, Word, and PowerPoint preferred
Benefits
10 month contract
Administrative shift
Company
BioPharma Consulting JAD Group
BioPharma Consulting JAD Group is a consulting company that provides solutions in the validation, engineering, and compliance fields.
51-200 employees
H1B Sponsorship
BioPharma Consulting JAD Group has a track record of offering H1B sponsorships. Please note that this does not
guarantee sponsorship for this specific role. Below presents additional info for your
reference. (Data Powered by US Department of Labor)
Distribution of Different Job Fields Receiving Sponsorship
Represents job field similar to this job
Trends of Total Sponsorships
2025 (2)
Funding
Current Stage
Growth StageLeadership Team
D
Diego Ramirez
Owner
Company data provided by crunchbase