Key Responsibilities:

Perform quality control tests on raw materials, in-process samples, and final products using established procedures and equipment.
Analyze and interpret test results, and report any deviations or issues to the appropriate teams.
Conduct environmental monitoring and equipment calibrations to ensure compliance with regulatory standards.
Develop and maintain quality control documentation, including Standard Operating Procedures (SOPs), test methods, and specifications.
Participate in the investigation of product failures and deviations to identify root causes and implement corrective and preventive actions.
Collaborate with cross-functional teams, including R&D, production, and regulatory affairs, to ensure compliance with quality standards.
Conduct internal audits to assess compliance with Good Manufacturing Practices (GMPs) and other regulatory requirements.
Stay up-to-date with industry trends and regulatory changes, and make recommendations for process improvements.
Assist in the training and development of new quality control team members.
Maintain a clean and safe working environment in accordance with company policies and procedures.

Qualifications:

Bachelor's degree in Biotechnology, Biology, Chemistry, or a related field.
Minimum of 3 years of experience in a quality control role in the biotechnology or pharmaceutical industry.
Strong understanding of GMPs and other regulatory requirements.
Experience with analytical techniques such as HPLC, GC, and PCR.
Excellent problem-solving and critical thinking skills.
Strong attention to detail and the ability to work independently.
Excellent communication and interpersonal skills.
Ability to multitask and manage competing priorities in a fast-paced environment.
Proficiency in Microsoft Office and other relevant software applications.
Flexibility to work outside of regular business hours when needed.

Join our team and help us make a positive impact on the world through our innovative biotechnology products.

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