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Job Requirements of Quality Control Analyst II:
-
Employment Type:
Contractor
-
Location:
Norton, MA (Onsite)
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Quality Control Analyst II
Careers Integrated Resources Inc
Norton, MA (Onsite)
Contractor
Pay $45/hr on w2
This is an on-site role in Norton, MA, with occasional responsibilities at other client locations. Weekend coverage is required. First shift, Friday-Monday (4 x 10 hours), with initial Monday-Friday training.
The Quality Control Operations (QCO) Analyst II Contractor supports maintaining high standards of quality and compliance from development through commercialization. The role includes performing routine and non-routine testing, participating in data trending, investigations, and lab operations, and supporting method transfers, qualification/validation, verification, and implementation.
This position enhances QC efficiency and effectiveness.
Key Responsibilities Perform routine/non-routine analytical (HPLC/UPLC) and/or microbiological assays for raw materials, in-process samples, product release, and stability studies following SOPs
Support weekend lab operations and maintain training records
Assist in lab equipment and inventory maintenance, including reagent and sample prep Review data timely and qualify as a data reviewer
Perform operational assignments (raw material processes, environmental monitoring, in-process testing) Contribute to updating controlled documents (SOPs, work instructions, test methods)
Follow internal policies, SOPs, and regulatory standards (GMP, GLP, ICH) Participate in continuous improvement initiatives and cross-functional collaboration Support regulatory submissions, inspection readiness, and audits
Qualifications B.S. in chemistry, biology, biochemistry, or related field 4-8 years of pharmaceutical/biotech experience in GMP QC or equivalent
Experience in method transfer/implementation; understanding of method lifecycle management preferred Strong technical writing, data analysis, problem-solving, and organizational skills
Excellent communication and teamwork Proficiency in LabWare LIMS, Excel, Word, and PowerPoint preferred
Additional Information:
WEEKEND SHIFT
This is an on-site role in Norton, MA, with occasional responsibilities at other client locations. Weekend coverage is required. First shift, Friday-Monday (4 x 10 hours), with initial Monday-Friday training.
The Quality Control Operations (QCO) Analyst II Contractor supports maintaining high standards of quality and compliance from development through commercialization. The role includes performing routine and non-routine testing, participating in data trending, investigations, and lab operations, and supporting method transfers, qualification/validation, verification, and implementation.
This position enhances QC efficiency and effectiveness.
Key Responsibilities Perform routine/non-routine analytical (HPLC/UPLC) and/or microbiological assays for raw materials, in-process samples, product release, and stability studies following SOPs
Support weekend lab operations and maintain training records
Assist in lab equipment and inventory maintenance, including reagent and sample prep Review data timely and qualify as a data reviewer
Perform operational assignments (raw material processes, environmental monitoring, in-process testing) Contribute to updating controlled documents (SOPs, work instructions, test methods)
Follow internal policies, SOPs, and regulatory standards (GMP, GLP, ICH) Participate in continuous improvement initiatives and cross-functional collaboration Support regulatory submissions, inspection readiness, and audits
Qualifications B.S. in chemistry, biology, biochemistry, or related field 4-8 years of pharmaceutical/biotech experience in GMP QC or equivalent
Experience in method transfer/implementation; understanding of method lifecycle management preferred Strong technical writing, data analysis, problem-solving, and organizational skills
Excellent communication and teamwork Proficiency in LabWare LIMS, Excel, Word, and PowerPoint preferred
Additional Information:
WEEKEND SHIFT
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