QC Supervisor

• 5+ to 7 years experience
• Seniority Level - Mid-Senior
• Management Experience Required - Yes
• Minimum Education - Bachelor's Degree
• Willingness to Travel - Never

• The ideal candidate will have a min of 5 years of experience working as a Supervisor in a QC pharma lab managing a minimum of 3 people.

• Develops, implements, and maintains the activities of quality control systems. Oversees development and implementation of standards, methods, and procedures for inspecting, testing, and evaluating the precision, accuracy, and reliability of company products. Contributes information to help develop budgets. Makes recommendations for corrective action necessary to assure conformity with quality specifications. Assures finished products conform to government and company standards and satisfy GMP regulations.

• Provide general or direct supervision to exempt employees and/or skilled nonexempt employees
• Act as advisor to unit or sub-units become actively involved as required to meet schedules or resolve problems
• Provides supervision on the floor enforcing compliance to data integrity, SOPs, specifications, methods, USP, and cGMP through real-time verifications of records, logbooks, chromatograms, sequences, etc.
• Helps analysts by troubleshooting methods, instrumentation, and execution of the tests.
• Schedules testing/review of raw materials, in-process, finished product, stability samples, complaint samples, samples from the process, and cleaning validation activities
• Exercise judgment within defined procedures and policies to determine appropriate action. Critically review data for anomalies or trends and approve data
• Lead and approve investigations of suspect or out-of-specification results. Ensures implementation of CAPA.
• May perform bench analysis, as needed
• Frequently interacts with subordinates, outside customers, and functional peer groups at various management levels
• Interaction normally requires the ability to gain the cooperation of others, conduct presentations of technical information concerning specific projects/schedules, etc. Contributes to cross-functional projects with a significant impact on the company
• Responsible for observing all Company, Health, Safety, and Environmental guidelines
• Duties and responsibilities are not limited to the work listed above and may include other assignments as necessary

• BS degree in a scientific discipline (Chemistry preferred) with 5+ years’ experience or MS with 3+ years of experience or a combination of experience and training.
• Pharmaceutical/lab experience preferred
• Proficiency in MS Word, Excel, and PowerPoint
• Strong interpersonal and organizational skills
• Supervisory experience

• Chemistry
• Quality Control
• Pharmaceutical
• Supervisor experience

Ohm Systems, Inc. specializes in IT and Healthcare staffing services, dedicated to linking highly skilled professionals with our public and private clients across the United States. Our track record showcases our commitment to delivering outstanding staffing and consultancy solutions to our clients. We prioritize diversity and inclusivity and take pride in being an employer that promotes equal opportunities and affirmative action. Our goal is to foster an inclusive work environment that embraces individuals from all backgrounds, irrespective of their gender, race, or orientation.