Program Manager
Job
Weiss-Aug MedPharma
Fairfield, NJ (In Person)
Full-Time
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Job Description
Description:
Join Weiss-Aug- A Leader in Precision Manufacturing and Innovation Be part of a company that's shaping the future of manufacturing where your ideas, skills, and passion matter.
- Weiss-Aug MedPharma needs the best minds in industry. Expanding our team is paramount, bringing in fresh perspectives, ideas and broad-based talent to further enhance our solution offerings, driving new growth and supporting our technology roadmap
- including the release of finished drug-delivery / combination devices and machined implants.
Responsibilities:
Analyze existing processes using data and present proposals on improvements. Implementation and verification of acceptance of proposed improvements. Participate as a member of the APQP Project Team. Participate as a member of the New Program Development/Quoting Team. Investigate and determine root cause(s) for internal and external complaints and/or quality rejections. (DPD, DPA's, 8D's, DMR) Lead or participate in trouble shooting of existing and new processes. Create and maintain process documentation. Train personnel as it relates to process documentation and procedures. Participate in ISO/QS internal and external audits. Promote cleanliness and safety policies and procedures throughout the entire Company. Stay current (magazines, trade shows, seminars, etc) on new technology as it relates to the Company's scope.Requirements:
BS degree in Industrial or Mechanical Engineering. Must possess good analytical and problem-solving skills and mechanical aptitude. 5 years minimum experience in a medium/high volume manufacturing environment. Must be driven self-starter that works with little supervision. Must have good written and verbal communication skills. Must possess the ability to multi-task and set priorities. Must be a Team player and have the ability to interact effectively with all departments within the Company. Must have good windows-based PC skills (Microsoft Office, Outlook, Excel, etc). ISO/QS knowledge preferred. Plastic Injection/Insert Molding and/or Progressive Stamping Experience a plus. This position is at our Fairfield, NJ location.Salary :
$80,000- $100,000 per year Other Benefits Include Medical, Dental and Vision 401 (k) with company match Holiday, Vacation and Sick Time Tuition Reimbursement Health Savings Accounts (HAS) Flexible Spending Accounts (FSA) Cigna Wellness Incentive Program Employee Assistance Program (EAP) Short Term Disability Group Life and Accidental Insurance Sun Life
- Accident, Critical Illness, and Hospital Indemnity Insurance Smoking Cessation Program Pet Insurance US Pay Transparency The base salary for this role will be determined on a case-by-case basis and may vary based on the following considerations: job-related knowledge and skills, experience, and internal consistency.
- $100,000 a year
- Full-time Weiss-Aug MedPharma 26 reviews $80,000
- $100,000 a year
Full-time Description:
Join Weiss-Aug- A Leader in Precision Manufacturing and Innovation Be part of a company that's shaping the future of manufacturing where your ideas, skills, and passion matter.
- Weiss-Aug MedPharma needs the best minds in industry. Expanding our team is paramount, bringing in fresh perspectives, ideas and broad-based talent to further enhance our solution offerings, driving new growth and supporting our technology roadmap
- including the release of finished drug-delivery / combination devices and machined implants.
Responsibilities:
Analyze existing processes using data and present proposals on improvements. Implementation and verification of acceptance of proposed improvements. Participate as a member of the APQP Project Team. Participate as a member of the New Program Development/Quoting Team. Investigate and determine root cause(s) for internal and external complaints and/or quality rejections. (DPD, DPA's, 8D's, DMR) Lead or participate in trouble shooting of existing and new processes. Create and maintain process documentation. Train personnel as it relates to process documentation and procedures. Participate in ISO/QS internal and external audits. Promote cleanliness and safety policies and procedures throughout the entire Company. Stay current (magazines, trade shows, seminars, etc) on new technology as it relates to the Company's scope.Requirements:
BS degree in Industrial or Mechanical Engineering. Must possess good analytical and problem-solving skills and mechanical aptitude. 5 years minimum experience in a medium/high volume manufacturing environment. Must be driven self-starter that works with little supervision. Must have good written and verbal communication skills. Must possess the ability to multi-task and set priorities. Must be a Team player and have the ability to interact effectively with all departments within the Company. Must have good windows-based PC skills (Microsoft Office, Outlook, Excel, etc). ISO/QS knowledge preferred. Plastic Injection/Insert Molding and/or Progressive Stamping Experience a plus. This position is at our Fairfield, NJ location.Salary :
$80,000- $100,000 per year Other Benefits Include Medical, Dental and Vision 401 (k) with company match Holiday, Vacation and Sick Time Tuition Reimbursement Health Savings Accounts (HAS) Flexible Spending Accounts (FSA) Cigna Wellness Incentive Program Employee Assistance Program (EAP) Short Term Disability Group Life and Accidental Insurance Sun Life
- Accident, Critical Illness, and Hospital Indemnity Insurance Smoking Cessation Program Pet Insurance US Pay Transparency The base salary for this role will be determined on a case-by-case basis and may vary based on the following considerations: job-related knowledge and skills, experience, and internal consistency.
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