Integrated Resources, Inc.
Job Title: Quality Control Analyst II
Job Location: Norton, MA
Job Duration: 10-11 Months (possibility of extension)
Payrate: $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.
Job Summary
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.
Education and Experience
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 Lab Ware LIMS, Excel, Word, and PowerPoint preferred.
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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.
Job Summary
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.
Education and Experience
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 Lab Ware LIMS, Excel, Word, and PowerPoint preferred.
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