2 Manufacturing jobs in Weaver
Manufacturing Equipment Senior Engineer
Posted today
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Job Description
What Makes a Honda, is Who makes a Honda
Honda has a clear vision for the future, and its a joyful one. We are looking for individuals with the skills, courage, persistence, and dreams that will help us reach our future-focused goals. At our core is innovation. Honda is constantly innovating and developing solutions to drive our business with record success. We strive to be a company that serves as a source of power that supports people around the world who are trying to do things based on their own initiative and that helps people expand their own potential. To this end, Honda strives to realize the joy and freedom of mobility by developing new technologies and an innovative approach to achieve a zero environmental footprint.
We are looking for qualified individuals with diverse backgrounds, experiences, continuous improvement values, and a strong work ethic to join our team.
If your goals and values align with Hondas, we want you to join our team to Bring the Future!
Job PurposeLeading a team in the development and improvement of Equipment Strategy and Business Plan to improve Safety, Quality, Cost, Delivery, Morale, Environment (SQCDME) targets.
Key Accountabilities- Supervising and leading a team of equipment engineers and technicians, including providing direction, training, and offering support.
- Monitors team performance, setting goals and conducting performance reviews to ensure the teams effectiveness.
- Support the resolution of equipment-related issues by identifying root causes, analysing data, and collaborating with cross-functional teams to implement effective solutions.
- Focus on optimizing equipment utilization, reduce waste and improve overall productivity within the production process.
- Promoting a culture of continuous improvement by encouraging innovative approaches in the engineering processes.
- Staying up-to-date with emerging technologies and trends to identify opportunities for enhancing equipment performance, efficiency and effectiveness.
- Works closely with cross functional teams to provide input on equipment requirements specifications, and performance improvements.
- Overseeing the installation, upgrading, and modification of equipment.
- Associate degree in Engineering.
- Minimum of 5 (years) of Project management/Equipment Experience.
- Ability to Lead Engineering Team.
- Ability to Schedule and prioritize task in dynamic environment.
- Office and Production Environment
- Must be able to work nights and weekends as required (New Model Launch, Weekend Work, Shutdown).
- Must be willing to travel as needed.
- Must be willing to work overtime as needed.
What differentiates Honda and make us an employer of choice?
Total Rewards:
- Competitive Base Salary (pay will be based on several variables that include, but not limited to geographic location, work experience, etc.)
- Paid Overtime
- Regional Bonus (when applicable)
- Industry-leading Benefit Plans (Medical, Dental, Vision, Rx)
- Paid time off, including vacation, holidays, shutdown
- Company Paid Short-Term and Long-Term Disability
- 401K Plan with company match + additional contribution
- Relocation assistance (if eligible)
Career Growth:
- Advancement Opportunities
- Career Mobility
- Education Reimbursement for Continued Learning
- Training and Development programs
Additional Offerings:
- Tuition Assistance & Student Loan Repayment
- Lifestyle Account
- Childcare Reimbursement Account
- Elder Care Support
- Wellbeing Program
- Community Service and Engagement Programs
- Product Programs
Honda is an equal opportunity employer and considers qualified applicants for employment without regard to race, color, creed, religion, national origin, sex, sexual orientation, gender identity and expression, age, disability, veteran status, or any other protected factor.
Manufacturing Technician I - Diluent (Anniston, AL)
Posted 1 day ago
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Job Description
The success of a company depends on the passionate people we partner with.
Together, let's share our talents.
As a global leader in animal health, Ceva Animal Health believes our success is linked to our passionate people researching, developing , producing and supplying innovative health solutions for all animals, which contributes to the future of our diverse planet.
We are committed to ensuring the highest possible level of care and well-being for farm animals (poultry, pigs, ruminants), companion animals (dogs and cats) and wildlife.
Indeed, Our "Together, Beyond Animal Health" vision emphasizes that the health and wellbeing of people, animals and our planet are totally interlinked. More than ever, Ceva is committed to a "One Health" approach.
As part of our "Diversity, Equity and Inclusion" policy, Ceva Animal Heath is committed to the employment of people with disabilities and will make reasonable accommodations throughout the interview process to ensure an inclusive and accessible experience for all applicants. To request an accommodation, please contact a member of the Ceva Talent Acquisition team.
Yourmissions :
Location: Anniston, AL
Job Summary and Purpose:
The Lab Technician I plays a key role in supporting production activities, with a primary focus on the manufacturing of sterile diluents. This role involves operating lab equipment such as autoclaves, batching tanks, filling machines, sealing machines, and labeling equipment. The technician ensures that all tasks and associated documentation are completed accurately and in a timely manner, including data entry into the JDE database. Additionally, the Lab Technician I may assist in the production of vaccines, shipping and receiving, and the operation of autoclaves as needed.
Responsibilities and Key Duties:
Diluent Production
• Accurately weigh and prepare chemicals required for diluent production.
• Prepare and batch sterile diluents according to production requirements.
• Operate filling and sealing equipment to produce I.V. bags.
Material Preparation and Packaging
• Assemble and label packaging materials for I.V. bags.
• Package finished products for shipment, ensuring compliance with quality standards.
• Assist in shipping diluents and vaccines as needed, ensuring proper handling and documentation.
Equipment Operation and Maintenance
• Operate and maintain production equipment, including autoclaves, labelers, sealers, pumps, scales, pH meters, osmometers and pallet lifter.
• Perform routine checks and basic troubleshooting to ensure optimal equipment functionality.
• Conduct daily, weekly, and monthly cleaning and sanitation of laboratory areas to maintain a sterile environment.
Documentation and Data Entry
• Complete all required production and quality documentation accurately and in real-time.
• Enter production data into the JDE database to ensure accurate record-keeping.
• Complete other duties as assigned.
Core Competencies:
• Shape solutions out of complexity
• Client focus
• Collaborate with empathy
• Engage and develop
• Drive ambition and accountability
• Influence others
Technical / Functional Competencies:
• Able to operate technical machinery and possibly computerized equipment
• Ability to understand and perform primary production procedures on equipment for which qualified and consult appropriate documentation when needed.
• Able to follow instructions and production schedules.
• Know and respect all regulations as well as health, safety, quality and environment standards applicable within the environment.
• Can use main IT tools to perform the job in production.
• Knowledgeable about lean philosophy and purpose.
• Can apply performance management tools per KPIs and participate in applying basic problem-solving skills.
• Ability to apply basic lean tools as per 5S, standard work.
• Understanding of production standards including time, raw materials/productivity, and final quantity.
• Capable of participating in a project to provide expertise and output.
• Able to demonstrate self-discipline and attention to detail
• Mathematical aptitude and computer skills
Qualifications:
Education - High school diploma or equivalent required. Associate/Bachelor's degree in Life Science, preferred
Work Experience - Experience in a biological laboratory or equivalent, preferred. Experience in a cGMP environment, preferred.
Other (consider certifications, specialized knowledge and/or training, etc.) - N/A
Physical Requirements:
• Able to read, write legibly and communicate in English
• Frequent squatting, bending and twisting
• Frequent standing and walking for extended periods of time - approximately 85% of the work day
• Lifting up to 50 pounds
• Frequent repetition of wrist and shoulder rotations
• Dexterity: frequent fine motor movements
• Visual inspection and interpretation of microscopic and color standards
• Ability to dress and operate in clean room environments
Working Conditions:
Clean room manufacturing laboratory
Travel Required:
N/A
This job description is intended to convey information essential to understanding the scope of the job and general nature and level of work performed by job holders within this job. This job description is not intended to be an exhaustive list of qualifications, skills, duties and responsibilities or working conditions associated with the job. This job description is not an employment contract. Ceva reserves the right to modify job duties and/or job descriptions at any time to meet the needs of the business.
*VEVRAA Federal Contractor
**Ceva is an equal opportunity employer and all qualified applicants will be considered for employment without regard to race, color, religion, sex, national origin, age, genetic information, actual or perceived sexual orientation, gender identity, disability status, protected veteran status, or any other characteristic protected by law. Ceva encourages men and women, members of all racial and ethnic groups, individuals with disabilities and veterans to apply.
669B
#USCEVA
Yourprofile :
Education - High school diploma or equivalent required. Associate/Bachelor's degree in Life Science, preferred
Work Experience - Experience in a biological laboratory or equivalent, preferred. Experience in a cGMP environment, preferred
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