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Job Description

We are seeking an experienced Operations Supervisor to oversee 75% of our operations lifecycle, including staging, filling, demolding, and other processes. This role will manage a team of 20 employees across four departments, ensuring efficient and compliant operations.

Key Responsibilities:

Supervise and coordinate daily operations across staging, filling, demolding, and other processes.

Manage and lead a team of 20 employees, providing guidance and support.

Ensure compliance with Good Manufacturing Practices (GMP) and quality standards.

Oversee safety documentation and ensure adherence to safety protocols.

Conduct regular quality checks and audits to maintain high standards.

Collaborate with other departments to optimize workflow and productivity.

Implement process improvements to enhance efficiency and reduce costs.

Required Qualifications:

Bachelor's degree in a related field (e.g., Engineering, Manufacturing, Operations Management).

Minimum of [X] years of experience in manufacturing, preferably in the medical device industry.

Proven experience in safety documentation and familiarity with GMP.

Strong leadership and team management skills.

Excellent organizational and problem-solving abilities.

Effective communication skills, both written and verbal.

Preferred Qualifications:

Experience with quality checks and audits in a manufacturing environment.

Knowledge of regulatory requirements for medical device manufacturing.

We are a company committed to creating inclusive environments where people can bring their full, authentic selves to work every day. We are an equal opportunity employer that believes everyone matters. Qualified candidates will receive consideration for employment opportunities without regard to race, religion, sex, age, marital status, national origin, sexual orientation, citizenship status, disability, or any other status or characteristic protected by applicable laws, regulations, and ordinances. If you need assistance and/or a reasonable accommodation due to a disability during the application or recruiting process, please send a request to Human Resources Request Form (https://airtable.com/app21VjYyxLDIX0ez/shrOg4IQS1J6dRiMo) . The EEOC "Know Your Rights" Poster is available here (https://www.eeoc.gov/sites/default/files/2023-06/22-088\_EEOC\_KnowYourRights6.12ScreenRdr.pdf) .

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Skills and Requirements

3 years experience in a leadership role within GMP environment

Familiar with GMP SOPs and documentation

Ability to lead a large operations team across 4 divisions

Demonstrated experience with quality checks

Experience in a regulated industry in manufacturing operations Medical device experience null

We are a company committed to creating diverse and inclusive environments where people can bring their full, authentic selves to work every day. We are an equal employment opportunity/affirmative action employer that believes everyone matters. Qualified candidates will receive consideration for employment without regard to race, color, ethnicity, religion,sex (including pregnancy), sexual orientation, gender identity and expression, marital status, national origin, ancestry, genetic factors, age, disability, protected veteran status, military oruniformed service member status, or any other status or characteristic protected by applicable laws, regulations, andordinances. If you need assistance and/or a reasonable accommodation due to a disability during the application or the recruiting process, please send a request to [email protected].