Quality Control Analyst II

Biopharma-Consulting-Jad-Group; Norton (MA); On-site; USD 55,000 - 83,000; Full time

Job summary

Biopharma-Consulting-Jad-Group seeks a QC Analyst II Contractor in Norton, MA to support high-quality analytical testing across development to commercialization. The role emphasizes routine and non-routine assays (HPLC/UPLC) and data review, with responsibilities spanning method transfers, documentation updates, and audits.

Your work will include weekend lab coverage, training record maintenance, and collaboration with cross-functional teams to ensure GMP, GLP, and ICH compliance while advancing

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.

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.

Skills

Data analysis

Technical writing

Problem solving

Organizational skills

LabWare LIMS

Excel

Word

PowerPoint

Education

B.S. in chemistry, biology, biochemistry, or related field

Tools

LabWare LIMS

Excel

Word

PowerPoint

Job description

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.

• 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.
• Strong technical writing, data analysis, problem-solving, and organizational skills.
• Proficiency in LabWare LIMS, Excel, Word, and PowerPoint.

• Contract position with possible extension
• Location: Norton, MA, with occasional responsibilities at other locations.
• Weekend coverage is required.
• First shift, Friday-Monday (4 x 10 hours), with initial Monday-Friday training.