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Quality Control Analyst - Contract - Norton, MA

ºÚÁÏÊÓƵ is working alongside a pharmaceutical company seeking a Quality Control Analyst to join their team in Norton, MA.

Primary Responsibilities:

The successful candidate will perform both routine and specialized analytical and microbiological assays to support various stages of product development and release. This position requires a commitment to maintaining high quality standards and supporting continuous laboratory operations, including weekend work.

Skills & Requirements:

• Proficiency in analytical and microbiological testing techniques.
• Ability to support continuous laboratory operations, including weekends.
• Strong organizational skills to maintain training records and adhere to schedules.
• Experience in maintaining laboratory equipment and inventory.
• Competence in data review and operational task management.
• Familiarity with regulatory standards and continuous improvement initiatives.
• Effective collaboration skills with cross functional teams.
• Commitment to ongoing professional development in QC testing and compliance.

The Quality Control Analyst's responsibilities will be:

• Conduct analytical and microbiological assays for raw materials, inprocess samples, and product release.
• Support weekend laboratory operations to ensure continuous workflow.
• Maintain training records and adhere to testing schedules for timely completion of assignments.
• Assist in maintaining laboratory equipment and inventory, including reagent and sample preparation.
• Review data promptly and qualify as a data reviewer for efficient data availability.
• Perform operational tasks such as raw material processing and environmental monitoring.
• Contribute to updating controlled documents to ensure compliance with industry standards.
• Adhere to internal and regulatory standards, including GMP, GLP, and ICH guidelines.
• Participate in continuous improvement efforts to enhance laboratory processes.
• Collaborate with QC and crossfunctional teams to support quality control operations.
• Engage in ongoing training to enhance expertise in QC testing and regulatory compliance.
• Assist in preparing technical documentation for regulatory submissions.
• Participate in inspection readiness activities and support audits and inspections.
• Collaborate with various organizational functions to align with business goals.

Compensation:

• $30.00 - $40.00 per hour

If you are having difficulty in applying or if you have any questions, please contact Shannon Briggs at s.brigg@proclinical.com

ºÚÁÏÊÓƵ is a specialist employment agency and recruitment business, providing job opportunities within major pharmaceutical, biopharmaceutical, biotechnology and medical device companies.

ºÚÁÏÊÓƵ Staffing is an equal opportunity employer.