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This is a senior-level position responsible for overseeing and supporting the work of junior chemists, managing, and maintaining lab instruments, analyzing data, identifying quality issues, and leading and managing validation projects. The primary responsibility of the QC Supervisor will be to lead and supervise the QC department, ensuring regulatory compliance and maintaining high-quality standards. You will be accountable for mentoring and managing a team of QC chemists and analysts.
Job Responsibility:
Conduct routine and non-routine analyses of raw materials, in-process samples, final products, and stability samples for product release
Utilize various analytical testing techniques such as Gas Chromatography (GC), UV-Visible spectroscopy, titrations, and other relevant methods
Provide guidance, support, and mentorship to foster professional growth and development within the team
Monitor compliance with established procedures, protocols, and regulatory requirements
Represent the QC department in cross-functional meetings and project teams
Review and revise quality control protocols and test plans to align with industry standards
Planning, scheduling, and coordinating analytical testing activities
Monitor the generation of analytical data by the QC team to ensure accuracy, integrity, and compliance
Assist the QC team in resolving technical problems related to instrumentation, method development, or other analytical issues
Interacts with internal and external customers to ensure proper sampling, reporting, and resolution of questions and concerns
Lead investigations into Out of Specification (OOS) test results, deviations, and non-conformances
Review, approve and validate data provided by other QC chemists
Maintains audit readiness within the department by collaborating with a cross-functional team, ensuring proper training of staff, reviewing documentation, and ensuring laboratory cleanliness
Provide technical review and approval of analytical test methods, validation protocols, risk assessments and Standard Operating Procedures (SOPs)
Manage validation protocols, including drafting, execution, and comprehensive documentation
Ensure all team members are trained in safety procedures, GMP requirements and laboratory best practices
Requirements:
Bachelor’s or master’s degree in chemistry, biochemistry, or a related field
Previous experience in a QC or quality role
3+ years of experience in supervisory or leading role
Strong supervisory, leadership, strategic thinking, and problem-solving skills
Excellent communication and organizational skills, with an ability to effectively communicate complex concepts to diverse stakeholders
Ability to manage multiple priorities under tight deadlines
Effective problem-solving and troubleshooting skills, with the ability to identify and address issues promptly
Excellent communication skills, both written and verbal, allowing for clear and concise reporting and collaboration with team members
Ability to work independently with minimal supervision while being a proactive and reliable team player
What we offer:
Formal and informal training opportunities
Comprehensive health and dental benefits
Income protection: short- and long-term disability coverage, life insurance, paid personal sick time
Vacation time exceeding industry standards
Company funded retirement savings program with individual contribution opportunities
Meaningful and challenging work
Curated intentional culture focused on growth and development, engagement, and communication
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