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Job type: Contract

Discipline: Good Manufacturing Practice (GMP)

Location: United States

GMP QC Analyst - Contract - Norton, MA

��Ƶ is on the hunt for bold, innovative thinkers who are ready to help push the boundaries of science and make a tangible difference in the world.

Primary Responsibilities:

This position is require to support analytical testing and quality control activities within a regulated laboratory environment. This role involves performing routine and non-routine assays, maintaining compliance with industry standards, and contributing to the continuous improvement of laboratory processes.

Skills & Requirements:

Degree in Chemistry, Biochemistry, Pharmaceutical Sciences, or a related field.
Familiarity with GMP/GLP-regulated laboratory environments, preferably within pharmaceutical or biotechnology industries.
Understanding of analytical techniques used in raw material testing, in-process testing, and stability studies is advantageous.
Strong documentation skills with attention to detail and a commitment to quality and compliance.
Basic knowledge of regulatory guidelines relevant to pharmaceutical quality control (e.g., GMP, GLP, ICH) is desirable.

The GMP QC Analyst's responsibilities will be:

Conduct analytical assays for raw materials, in-process samples, product release, and stability studies following established procedures.
Maintain training records, adhere to testing schedules, and ensure timely completion of assignments to meet project timelines and quality standards.
Assist in laboratory operations, including equipment maintenance, inventory management, and preparation of reagents and samples.
Accurately document experimental data and observations in compliance with GxP standards.
Participate in data review and contribute to updating controlled documents such as SOPs, work instructions, and test methods.
Ensure adherence to internal policies, SOPs, and regulatory standards (e.g., GMP, GLP, ICH guidelines).
Identify and suggest improvements to laboratory methods and processes to enhance efficiency and reliability.
Collaborate with cross-functional teams to support seamless quality control operations.
Pursue ongoing training to deepen expertise in analytical techniques and regulatory compliance.

Compensation:

$25 to $30 per hour

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

If you are interested in applying to this exciting opportunity, then please click 'Apply' or to speak to one of our specialists please request a call back at the top of this page.

��Ƶ is a leading life sciences recruiter focused on finding exceptional people and matching them with the finest positions across the globe. ��Ƶ is acting as an Employment Agency in relation to this vacancy.

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