Job Description
Work Schedule 12 hr shift/days Environmental Conditions Adherence to all Good Manufacturing Practices (GMP) Safety Standards, Cleanroom: no hair products, jewelry, makeup, nail polish, perfume, exposed piercings, facial hair etc... allowed, Office, Some degree of PPE (Personal Protective Equipment) required (safety glasses, gowning, gloves, lab coat, ear plugs etc.) As part of the Thermo Fisher Scientific team, you’ll discover meaningful work that makes a positive impact on a global scale. We provide our global teams with the resources needed to achieve individual career goals while helping to take science a step beyond by developing solutions for some of the world’s toughest challenges, like protecting the environment, making sure our food is safe or helping find cures for cancer. Location/Division Specific Information Greenville, NC - Pharmaceutical Services Group - Steriles Hours: 6AM - 6PM (2/2/3 rotation) Relocation assistance is NOT provided Must be legally authorized to work in the United States without sponsorship. Must be able to pass a comprehensive background check, which includes a drug screening. Position summary: The B52 Supervisor (Vial Line 9) supervises work teams and provides leadership to production colleagues in the manufacturing and filling of high-quality pharmaceutical products according to schedule, cost, and quality standards. As the supervisor, you will play a crucial role in maintaining human relations, safety performance, and ensuring adherence to all regulatory control and documentation procedures. Additionally, you will handle Production/Engineering related projects to increase production efficiencies and add flexibility to support our customers. Key Responsibilities: Provide exceptional leadership to assigned staff by leading organizational change and empowering them to succeed. Cultivate strong relationships and build effective teams that apply their diverse skills and perspectives to achieve common goals. Ensure that established standards, including production, quantity, and quality, are met. Take direct action to correct deviations and report variances and exceptions to the assigned position supervisor. Ensure that all production operations are validated and fully follow all Current Good Manufacturing Practices (cGMPs). Maintain compliance for the FDA, QAT, and OSHA inspections. Use available resources effectively to plan, monitor, and revise daily production schedules as necessary. Your goal is to produce a quality product in an efficient manner. Administer department safety programs to promote a culture of safety and ensure that operative personnel understand and follow safety rules and procedures. Evaluate performance and skills of personnel and provide constructive feedback for continuous improvement. Take corrective action when required and perform annual employee evaluations. Assist technical staff and customers in resolving technical issues to ensure new transferred processes are robust and validated. Develop and validate the technical requirements for production documentation, such as equipment and systems specifications, manufacturing formulas, procedures, work orders, and other relevant information. Implement cost reduction programs to stay competitive in the present economy. Track employees' attendance, approve time cards, and ensure completion of required trainings. Perform other duties as assigned. Qualifications: Bachelor's degree in Physical, Biological, Chemical, or Production related science strongly preferred. Equivalent experience in these fields will also be considered. 5+ years of manufacturing experience with 2 years of prior leadership experience required. Experience in a Steriles pharmaceutical manufacturing environment is preferred. Equivalent education and experience can be considered. Technical and operational knowledge of aseptic processing operations, ability to handle multiple ongoing activities, and prioritize tasks. Outstanding attention to detail and organizational skills. Self-starter, mature, independent, and dependable. Ability to work in a fast-paced environment under pressure, multitask, and drive for results. Demonstrates ability to maintain a high degree of confidentiality. Effective time management and prioritization skills. Requires discretion and independent judgment. Very high degree of interpersonal skills to establish and maintain effective working relationships with employees and the public. Highly effective verbal and written communication skills. Demonstrated ability to manage and lead professional staff t