Quality Control Analyst III - Contract - Norton MA
Proclinical is seeking a dedicated Quality Control Analyst III to support the department's commitment to maintaining high standards of quality and compliance from development through commercialization.
Primary Responsibilities:
This role will be involved in routine and non-routine testing, data trending, investigations, and laboratory operations. This position requires flexibility for weekend coverage and is primarily based onsite in Norton, MA.
Skills & Requirements:
Degree in chemistry, biology, biochemistry, or related scientific field.
Experience in a GMP Quality Control function within the pharmaceutical/biotech industry.
Knowledge of method transfer and analytical method implementation.
Strong technical writing skills, particularly for investigations.
Proficient in data analysis and interpretation with attention to detail.
Problem-solving skills and experience in conducting investigations and implementing CAPA.
Strong organizational skills and ability to manage multiple tasks.
Excellent communication and teamwork abilities.
Proficiency in LabWare LIMS, Excel, Word, and PowerPoint preferred.
The Quality Control Analyst's responsibilities will be:
Conduct routine and non-routine analytical and microbiological assays for raw materials, in-process samples, product release, and stability studies.
Support weekend laboratory operations to maintain a continuous operational schedule.
Maintain training records, adhere to testing schedules, and ensure 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 assignments such as raw material processes and environmental monitoring.
Contribute to revising and updating controlled documents to ensure compliance with industry standards.
Adhere to internal and regulatory standards to maintain quality and compliance.
Participate in continuous improvement efforts to enhance laboratory processes.
Collaborate with QC and cross-functional teams to support seamless operations.
Pursue ongoing training to deepen expertise in QC testing techniques and regulatory compliance.
Assist in preparing technical documentation for regulatory submissions.
Participate in inspection readiness activities and support audits and inspections.
Collaborate with other organizational functions to align with business goals.
If you are having difficulty in applying or if you have any questions, please contact Anderson Maldonado at a.maldonado@proclinical.com
Proclinical is a specialist employment agency and recruitment business, providing job opportunities within major pharmaceutical, biopharmaceutical, biotechnology and medical device companies.
Proclinical Staffing is an equal opportunity employer.