Supervisor, Senior Team Leader (2nd Shift) (Bothell, WA)

Bausch & Lomb GmbH; Bothell (WA); On-site; USD 71,000 - 105,000; Full time

Job summary

Ein etabliertes Unternehmen im Gesundheitswesen sucht einen erfahrenen Produktionssupervisor für die 2. Schicht. In dieser spannenden Rolle sind Sie verantwortlich für die Überwachung des Produktionspersonals und die Gewährleistung der effizienten Nutzung von Ressourcen in der Herstellung von Medizinprodukten. Sie werden die Produktionsabläufe leiten, technische Probleme lösen und eng mit anderen Abteilungen zusammenarbeiten, um die Produktionsziele zu erreichen. Wenn Sie eine proaktive und verantwortungsbewusste Person sind, die in einem dynamischen Umfeld arbeiten möchte, ist dies die perfekte Gelegenheit für Sie, einen bedeutenden Beitrag zu leisten.

Qualifications

• Mindestens 5 Jahre Erfahrung in der Produktion von Medizinprodukten.
• Mindestens 3 Jahre Erfahrung in der Führung von Mitarbeitern in einem GMP-Umfeld.

Responsibilities

• Überwachung des Produktionspersonals und der Arbeitsabläufe.
• Sicherstellung der Einhaltung von Qualitätsstandards und Sicherheitsvorschriften.

Skills

Produktionsüberwachung

Mitarbeiterführung

Problemlösungsfähigkeiten

Analytische Fähigkeiten

GMP-Kenntnisse

Education

Bachelor of Arts oder Bachelor of Science in Engineering

Tools

MS Project

Visio

ERP-Systeme

Job description

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Supervisor, Senior Team Leader (2nd Shift) (Bothell, WA)

Join a team! We are a global diversified pharmaceutical company enriching lives through our relentless drive to deliver better health outcomes. We develop, manufacture and market a range of products, primarily in gastroenterology, hepatology, neurology, dermatology, medical aesthetic devices, international pharmaceuticals. Our 7,000 employees share a common goal and values, propelling us to provide essential care to millions of people globally. We seek dedicated individuals who share our sense of urgency, unity, and excellence.

We are looking for a trustworthy and respectful individual who consistently does the right thing. Someone who is imaginative and proactive, with a keen eye for what is possible. A perceptive and adaptive person who is action oriented. We need a disciplined, focused, and accountable team member. If you embody these values, come join our company and help us shape the future.We are all in it together to make a difference. Be a part of a culture that doesn't just wait for change but actively creates it—where your skills and values drive our collective progress and impact.

Supervisor, Sr. Team Leader, 2nd Shift (2:30pm-11pm)

Job Summary:

The Production Supervisor is responsible for overseeing production personnel, managing workflow, and ensuring the effective utilization of equipment, materials, and labor resources in the Medical Device manufacturing areas.

Principle Responsibilities and Duties:

Note: The following are meant to be representative but not necessarily all inclusive of the duties and responsibilities for this position title.

Primarily responsible for overseeing the product flow, addressing technical issues, and managing employee relations within the Production areas.

Meets production deadlines and efficiency goals.

Recommends and implements measures to enhance production methods and product quality in accordance with company guidelines.

Interprets company policies with precision and ensures the enforcement of safety regulations.

Ensuring the accuracy and completeness of the Device History Record for production completed by direct reports.

Creates staffing and training plans based on projected build schedules.

Conducts periodic employee assessments and evaluations.

Supports New Product Introduction activities

Oversee production staff involved in the manufacturing of medical device products.

Ensure production follows established quality standards and manufacturing SOPs.

Oversee the production process and ensure the efficient use of equipment, materials, and human resources.

Collaborate with the Planning department to comprehend the production schedule and ensure that production requirements are met promptly.

Collaborate with QA and Engineering teams to address and resolve production line quality issues. Oversee and report on area safety and housekeeping standards.

Assist with hiring and training employees.

Address and report employee issues. Track attendance and performance. Collaborate with HR and senior management for disciplinary actions.

Work on and facilitate projects aimed at continuous improvement.

Collaborate extensively with support departments such as Planning, Purchasing, Warehouse, Quality, Manufacturing Engineering, and Research & Development Engineering.

Level of Supervision Required

Work effectively with minimal supervision in team and individual situations.

Takes direction from Manufacturing Manager

Five or more years of directly related production experience in high mix, low volume medical device manufacturing environment.

Minimum 3 years of manufacturing supervisory experience in GMP environment, specifically assembly and packaging of medical devices.

Education: Bachelor of Arts or Bachelor of Science in Engineering or a related discipline.

Proficient in basic computer skills, including Word, Excel, and PowerPoint. Capable of learning and adapting to new software applications such as MS Project, Visio, ERP systems, and others as required.

Proficient in interpersonal, organizational, and motivational skills; possesses strong analytical capabilities.

Outstanding problem-solving abilities

Preferred: supervisory training.

Lean and Six Sigma (Greenbelt/Blackbelt) training a plus.

Clear understanding of GMPs and FDA regulatory guidelines.

Language and Verbal Skills

The ability to communicate proficiently in English verbally and in writing is required as well as being able to understand and follow work instructions in writing or when conveyed verbally.

Math Skills

Basic math skills, plus ability to apply concepts such as fractions, percentages, ratios, and proportions to practical situations.

Analytical and Reading Skills

Ability to read, interpret and follow company procedures, work instructions and engineering drawings and sketches. Ability to identify problems and deviations from prescribed specifications and requirements.

Physical Requirements

While performing the duties of this job, the employee is regularly required to perform light material handling tasks involving lifting weights of up to 35 pounds for short durations. Duties also may involve keyboard data entry.

Most work will be performed in a light-manufacturing environment. The noise level in the work environment is usually low to moderate.

Safety

Solta Medical is committed to the health and safety of our employees. We expect that all employees will perform their responsibilities while maintaining a safe, cooperative, and productive work environment, thus ensuring the health and safety of themselves and others.

As required by law,Bausch Health provides a reasonable range of compensation for roles that may be hired in the US. Actual compensation is influenced by a wide array of factors including but not limited to skill set, level of experience, and specific office location. For this role, the range of starting pay for this role is$71K to $105K per year.

We are an Equal Opportunity Employer. All qualified applicants will receive consideration for employment regardless of race, color, religion, sex, national origin, disability, military and/or veteran status, or any other Federal or State legally protected classes.

If a candidate needs a reasonable accommodation/adjustment due to physical or mental health impairment for any part of the application process, they are encouraged to send their request [e-mail] or call 908-927-1400 and let us know the nature of the request and their contact information.Please be sure to include the job requisition number.

Job Applicants should be aware of job offer scams perpetrated through the use of the Internet and social media platforms.