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Job Requirements of Quality Control Analyst:
-
Employment Type:
Contractor
-
Location:
Norton, MA (Onsite)
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Quality Control Analyst
Careers Integrated Resources Inc
Norton, MA (Onsite)
Contractor
Job Title: Quality Control Analyst
Location: Norton, MA
Duration: 12 months+
Pay Rate: $45/hr. on W2
First shift, Friday - Monday (4 x 10 hours), with initial Monday-Friday training.
Summary:
Key Responsibilities:
Qualifications:
Location: Norton, MA
Duration: 12 months+
Pay Rate: $45/hr. on W2
First shift, Friday - Monday (4 x 10 hours), with initial Monday-Friday training.
Summary:
- 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.
- First shift, Friday-Monday (4 x 10 hours), with initial Monday-Friday training.
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
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