Quality Control Supervisor Jobs

Janssen Pharmaceuticals, Inc, is hiring for a Quality Control Supervisor at our Athens, GA location!

At the Janssen Pharmaceutical Companies of Johnson & Johnson, we are working to create a world without disease. Transforming lives by finding new and better ways to prevent, intercept, treat and cure disease inspires us. We bring together the best minds and pursue the most promising science. We are Janssen. We collaborate with the world for the health of everyone in it. Learn more at www.janssen.com and follow us @JanssenGlobal.

Benefits you will enjoy starting your first day:

• Overtime compensation for salaried employees
• Full medical, dental and vision coverage
• Tuition Reimbursement for eligible degree programs
• Competitive 401k match, HSA/FSA, Pension, yearly Wellness subsidy
• 15 days paid vacation, plus 40 hours paid sick leave and additional 40 hours paid personal leave
• Relocation assistance available for qualified candidates outside of the 50-mile radius of Athens, GA.

Are you interested in joining a team that is positively impacting patients' lives by ensuring high quality in our pharmaceutical products? Apply today for this exciting role!

As a Quality Control Supervisor, you will,

Own the responsibility for leading and coordinating the activities of the Quality Control associates engaged in receiving, testing, and inspecting products, raw materials, intermediates or performing microbiology testing to ensure compliance with quality standards and production schedules.

The QC Supervisor also works with the team to identify, facilitate and direct projects and long-term goals for the laboratory, ensures enterprise goals and policies are implemented, and works with internal and external groups (which includes intra-site and across JSC One Lab) to ensure success. This role will also provide technical support and regulatory guidance, as it relates to lab operations and processes. The Supervisor will Seek continuous process improvements in terms of cost, processes, procedures, etc. to find efficiencies, and remove nonvalue-added activities, all while ensuring the highest level of quality and compliance.

Responsibilities

• Acts as a champion with regards to upholding the Credo, promotes continuous growth of self and others to be their best, and being a leader in terms of Safety.
• Communicates metrics and systems used to measure and guide improvements to product and system quality and customer satisfaction to quality control staff.
• Utilizes cost control initiatives to reduce expenses and provide input to budget planning process.
• Resolves complex investigations, driving to root cause and implementing effective corrective and preventive actions.
• Supervise, mentor, train, evaluate performance and provide growth opportunities for the quality control staff.
• Drives timely closure of laboratory investigations
• Develop and champion an organization of professionals that is able to apply innovation and creativity to technical and managerial challenges.
• Ensures regulatory compliance of laboratory operations, serves as a SME during audits and inspections.
• Implements methods and procedures for inspection, testing and evaluation
• Reviews processes to verify that prompt and appropriate actions and associated corrections are taken, when gaps are identified
• Provides input to quality control reports, requirements, and other information in response to requests for proposals, quotes, and other business opportunities.
• Leads projects such as method transfers, validations, equipment purchase and validations
• Communicates department objectives and metrics

Qualifications

• Able to motivate associates preferred.
• 4+ Experience with laboratory processes and practices, including cGMP compliance regulations required.
• Experience with quality auditing/evaluation techniques preferred.
• Capable of making all decisions that are required to effectively manage the laboratory teams and be able to acknowledge and discuss with upper management, the resulting interdependencies, and impacts required.
• Possess sound scientific and development practices, scientific terminology, company Quality Assurance procedures and policies preferred.
• A Bachelor’s degree in Chemistry or closely related science degree is required.
• Supervisory or team/project leadership experience required.
• Professional experience with HPLC, UPLC, GC, Wet Chemistry, and Chromatography software.
• Be able to establish priorities, delegate responsibilities, and train, supervise and develop leaders and associates required.
• Be detail oriented, have excellent communication, organization, investigation, and negotiation/influencing skills preferred.

Johnson & Johnson is an Affirmative Action and Equal Opportunity Employer. All qualified applicants will receive consideration for employment without regard to race, color, religion, sex, sexual orientation, gender identity, age, national origin, or protected veteran status and will not be discriminated against on the basis of disability.

For more information on how we support the whole health of our employees throughout their wellness, career and life journey, please visit www.careers.jnj.com (http://www.careers.jnj.com).