Apply on Employer Site

Johnson & Johnson Innovative Medicine · 14 hours ago

Quality Control Supervisor

Athens, GA

Full-time

Onsite

Mid, Senior Level

2+ years exp

Johnson & Johnson is a leader in healthcare innovation, aiming to develop treatments and cures for complex diseases. The Quality Control Supervisor is responsible for managing Quality Control associates, ensuring compliance with quality standards, and overseeing laboratory operations to guarantee the timely release of high-quality products.

Pharmaceuticals

Responsibilities

Provide technical and regulatory guidance related to lab operations and seek continuous process improvements in cost, quality, and compliance

Participate in global initiatives, perform gap assessments, provide input for quality control reports, budget planning, and project leadership on method transfers, validations, and equipment purchases

Uphold the Johnson & Johnson Credo, promoting safety and personal development while ensuring regulatory compliance of laboratory operations

Serve as an SME or in a support role for inspections and audits

Assure all laboratory responsibilities are performed in accordance with internal and external regulations and policies and consistent with supply chain cycle time goals

Contribute insights to address intricate investigations, focusing on identifying the root cause and implementing effective corrective and preventive measures, all while ensuring the prompt resolution of laboratory inquiries

Mentor and supervise quality control employees, evaluate performance, and conveys goals effectively to enhance product quality and customer satisfaction

Qualification

Microbiology LaboratoryPharmaceutical MicrobiologyQuality Control (QC)CGMP complianceQuality AuditingAseptic techniquesCompliance ManagementInclusive LeadershipQuality StandardsQuality Systems DocumentationReport WritingTechnologically SavvyCollaboratingLeadership

Required

A minimum of bachelor's degree in microbiology or a related science field is required

A minimum of 2 years of work experience in microbiology laboratory within the pharmaceutical industry is required

Proficient in Microbiology laboratory processes and practices, with a strong understanding of cGMP compliance regulations is required

Experience in aseptic techniques is required

This position may require availability for working multiple shifts, including irregular (non-standard) shifts and/or weekends

Preferred

Experience with Contamination Control Strategy Programs, scientific terminology, and Quality Assurance procedures and policies

Experienced in quality auditing and evaluation techniques

Capable of establishing priorities, delegating responsibilities, and training and developing leaders and team members

Ability to inspire and motivate associates, fostering a collaborative project team environment

Highly detail-oriented with excellent communication, organizational, investigative, and negotiation/influencing skills

Must possess the capability to make crucial decisions for effectively managing laboratory teams while recognizing and discussing interdependencies and impacts with upper management

Decisions and problem-solving in this role must align with higher-level organizational and business needs, ensuring full consideration of regulatory requirements, sound business practices, and scientific validity

Must demonstrate strong organizational agility, enabling rapid and effective responses to dynamic business needs

Responsibilities include adhering to all state and federal regulations, including FDA, EPA, OSHA, and DEA guidelines, as well as following company and site-specific policies and procedures