Manufacturing Excellence Specialist Job at Nestle Health Science (Eau Claire)

Operational Excellence Specialist

ABOUT THE JOB Business Performance Measurement Conduct time and motion studies t...

Location

Singapore

Salary:

Not provided

Amaris Consulting

Expiration Date

Until further notice

Requirements

Bachelor’s degree in Industrial Engineering, Operations Management, or a related field
At least 2 years’ experience in manufacturing or operations management
Strong knowledge of lean methodologies
Hands-on experience with time and motion studies, data visualization, and reporting
Proficiency in Microsoft PowerBI and digitalization tools
Excellent communication, cultural awareness, and ability to engage stakeholders at all levels
High learning agility and proven track record of delivering results

Job Responsibility

Conduct time and motion studies to optimize workflows and resource utilization
Apply statistical methods to analyze data, identify root causes, and recommend solutions
Support functional performance tracking and reporting using data visualization tools (e.g., PowerBI)
Lead and execute Operational Excellence (OpEx) initiatives within agreed timelines
Collaborate with stakeholders across all levels of the organization to align on goals and expectations
Drive effective change management to ensure successful adoption of new processes and tools
Identify and implement opportunities to reduce waste, maximize resources, and boost productivity
Co-facilitate workshops to uncover process improvement areas
Integrate appropriate digitalization solutions to streamline operations

What we offer

Global Diversity: Be part of an international team of 110+ nationalities
Trust and Growth: With 70% of our leaders starting at entry-level
Continuous Learning: Unlock your full potential with our internal Academy and over 250 training modules
Vibrant Culture: Enjoy a workplace where energy, fun, and camaraderie come together through afterworks, networking events, and more
Meaningful Impact: Join us in making a difference through our CSR initiatives, including the WeCare Together program

Fulltime

Specialist Manufacturing: NPI, Process Owner

Be part of Amgen's newest and most advanced drug substance manufacturing plant. ...

Location

United States , Holly Springs

Salary:

114990.00 - 139433.00 USD / Year

Amgen

Expiration Date

Until further notice

Requirements

High school diploma / GED & 10 years of biotechnology operations experience
Associate’s degree & 8 years of biotechnology operations experience
Bachelor’s degree and 4 years of biotechnology operations experience
Master’s degree in chemistry, biology, or engineering & 2 years of biotechnology operations experience
Doctorate degree
Degree in Chemical Engineering, Industrial Engineering, Biology, or Biochemistry
Excellent cross-functional project management, meeting facilitation, and technical writing skills
Experience in Downstream GMP manufacturing operations
Strong technical knowledge of drug substance processing (harvest, chromatography, filtration, buffer preparation) and a broad understanding of related disciplinary areas in bioprocessing
Ability to organize, analyze and interpret technical data through trend analysis, forecasting, modeling, etc.

Job Responsibility

Communicate and interface between the GMP manufacturing teams in the Amgen North Carolina (ANC) Biologics Drug Substance Manufacturing plant and Process Development scientific groups
Ensure new products are successfully introduced into ANC’s biologics manufacturing facility and ownership of downstream unit operations
Host cross-functional meetings to drive to timelines to support the tech transfer of the program into the facility as well as process ownership for some downstream process unit operations
New Product Introduction (NPI) lead coordinating with Manufacturing, Process Development, Supply Chain, Planning, Facilities and Engineering, as well as Quality to introduce new Drug Substance products and/or advanced technologies into the plant using project management tools (i.e. Smartsheet)
Downstream biologics drug substance technical expert who leads or participates in projects, including aiding in commissioning and qualification and training staff on equipment and processes
Support Manufacturing in troubleshooting, problem solving and RCAs
Support CAPA development to prevent error recurrence
Owns New Product Introduction Change Controls and collaborates with stakeholders to drive on-time completion
Responds to regulatory questions and/or audit findings
Ensures that manufacturing production documents (e.g. Standard Operating Procedures) are accurate and up to date

What we offer

Competitive and comprehensive Total Rewards Plans that are aligned with local industry standards

Fulltime

Specialist Manufacturing - Drug Product Operations

Join Amgen’s Mission of Serving Patients. At Amgen, our mission—to serve patient...

Location

United States , Thousand Oaks

Salary:

114990.00 - 139433.00 USD / Year

Amgen

Expiration Date

Until further notice

Requirements

Doctorate degree
Master’s degree and 2 years of Manufacturing support experience
Bachelor’s degree and 4 years of Manufacturing support experience
Associate’s degree and 8 years of Manufacturing support experience
High school diploma / GED and 10 years of Manufacturing support experience

Job Responsibility

Initiate, revise, and approve controlled manufacturing documents within Amgen’s electronic document management system (CDOCs)
Serve as document author, owner, reviewer, or data verifier
Maintain documentation to accurately reflect operational practices and regulatory requirements
Support implementation of new processes, equipment, and major initiatives within Drug Product operations
Collaborate with Capital, Engineering, Process Development, Quality, and other functions to define requirements and achieve operational readiness
Assist in developing and implementing SOPs, batch records, training, validation, and automation configurations
Analyze manufacturing data and performance metrics to identify trends, deviations, and opportunities for improvement
Develop and implement data-driven solutions to improve yield, reliability, and compliance
Support data monitoring using analytical tools such as Enterprise Data Lake and Spotfire
Support timely investigation and resolution of manufacturing deviations

What we offer

A comprehensive employee benefits package, including a Retirement and Savings Plan with generous company contributions, group medical, dental and vision coverage, life and disability insurance, and flexible spending accounts
A discretionary annual bonus program
Stock-based long-term incentives
Award-winning time-off plans
Flexible work models where possible

Fulltime

Specialist Manufacturing: NPI, Upstream Process Owner

Be part of Amgen's newest and most advanced drug substance manufacturing plant. ...

Location

United States , Holly Springs

Salary:

114990.00 - 139433.00 USD / Year

Amgen

Expiration Date

Until further notice

Requirements

High school diploma / GED & 10 years of biotechnology operations experience
Associate’s degree & 8 years of biotechnology operations experience
Bachelor’s degree and 4 years of biotechnology operations experience
Master’s degree in chemistry, biology, or engineering & 2 years of biotechnology operations experience
Doctorate degree
Degree in Chemical Engineering, Industrial Engineering, Biology, or Biochemistry
Excellent cross-functional project management, meeting facilitation, and technical writing skills
Experience in Upstream GMP manufacturing operations
Strong technical knowledge of Upstream drug substance processing (media preparation, cell culture, harvest) and a broad understanding of related disciplinary areas in bioprocessing
Ability to organize, analyze and interpret technical data through trend analysis, forecasting, modeling, etc.

Job Responsibility

Communicate and interface between the GMP manufacturing teams in the Amgen North Carolina (ANC) Biologics Drug Substance Manufacturing plant and Process Development scientific groups
Ensure new products are successfully introduced into ANC’s biologics manufacturing facility and ownership of upstream unit operations
Host cross-functional meetings to drive to timelines to support the tech transfer of the program into the facility as well as process ownership for some upstream process unit operations
New Product Introduction (NPI) lead coordinating with Manufacturing, Process Development, Supply Chain, Planning, Facilities and Engineering, as well as Quality to introduce new Drug Substance products and/or advanced technologies into the plant using project management tools (i.e. Smartsheet)
Upstream biologics drug substance technical expert who leads or participates in projects, including aiding in commissioning and qualification and training staff on equipment and processes
Support Manufacturing in troubleshooting, problem solving and RCAs
Support CAPA development to prevent error recurrence
Owns New Product Introduction Change Controls and collaborates with stakeholders to drive on-time completion
Responds to regulatory questions and/or audit findings
Ensures that manufacturing production documents (e.g. Standard Operating Procedures) are accurate and up to date

What we offer

Competitive and comprehensive Total Rewards Plans that are aligned with local industry standards

Fulltime

Contract Manufacturing (CM) Specialist

Location

Malaysia , Johor Bahru

Salary:

Not provided

Cricut

Expiration Date

Until further notice

Requirements

English fluency (written and spoken) is a must
mandarin and/or Malay is a plus
Advanced knowledge on Microsoft Excel, Word & power point. (lookup, Pivot, formula)
Bachelor’s degree in any field.
2-3 years working experience.

Job Responsibility

Assist in managing assigned Contract Manufacturers against Quality, supply & cost objectives throughout the product lifecycle.
Assist in Analyse and benchmark all CM (contract manufacturers) costed BOM submissions VS Internal BOM with assistance from component sourcing managers
Assist on CM Quarterly PPV claim
Responsible for monitoring CM delivery status on a weekly basis.
Responsible for checking all the quotations submitted by CM
PO Issuance
Oversee all day-to-day commercial issues/escalations from CM & internal stakeholders

What we offer

outstanding medical, dental, vision, and retirement benefits
pet insurance
401K match
life insurance
incentive programs
paid time off
on-site massages
phenomenal work-life balance
employee discounts

Fulltime

Continuous improvement specialist – food manufacturing

We are seeking a motivated and detail-oriented intern to support the development...

Location

Canada , North York

Salary:

25.00 CAD / Hour

Randstad

Expiration Date

February 24, 2026

Requirements

Currently enrolled in a post-secondary program in Food Science, Engineering, Operations Management, or related field
Strong analytical and problem-solving skills
Familiarity with Lean Manufacturing, Six Sigma, or Continuous Improvement methodologies is an asset
Proficient in Microsoft Excel and data visualization tools
Excellent communication and teamwork skills

Job Responsibility

Data Analysis & Reporting: Collect and analyze data on milk rework and dump occurrences
Identify trends, patterns, and root causes using tools such as Pareto charts and root cause analysis
Process Mapping & Documentation: Document current workflows related to milk handling and rework
Assist in creating standardized procedures and visual controls
Continuous Improvement Projects: Support CI initiatives using Lean and Six Sigma principles
Develop and implement corrective and preventive actions to reduce waste
Collaboration: Work closely with production, quality, and maintenance teams to gather insights and validate solutions
Participate in cross-functional meetings and present findings
Performance Tracking: Create dashboards or reports to monitor progress and KPIs related to milk rework and dumps

What we offer

Learning Opportunities: Hands-on experience in process optimization within a food manufacturing environment
Exposure to Lean and Six Sigma tools
Opportunity to contribute to sustainability and cost-saving initiatives

Inventory Accounting Specialist

Robert Half is seeking a detail-oriented Inventory Accounting Specialist for a c...

Location

United States , Marion, IA

Salary:

Not provided

Robert Half

Expiration Date

Until further notice

Requirements

Experience in inventory handling within the manufacturing industry
Proficiency in Excel, including pivot tables and VLOOKUPs
Familiarity with ERP systems
Strong attention to detail and problem-solving skills
Ability to adapt to new tools and processes
Excellent communication skills

Job Responsibility

Review new and existing parts to verify accurate costing and ensure proper setup in ERP system
Perform data entry for standard cost adjustments and updates based on purchasing information extracted from the ERP system
Populate cost data within the ERP system to ensure consistency and accuracy
Manage cycle count adjustments, prepare cycle count reporting, and track monthly adjustments
Pull cycle count reports and distribute them to relevant teams for action
Correct transactional errors identified by internal teams
update and resolve issues directly in the ERP system
Monitor and track rates for inventory accuracy, returns, defective parts, and cost adjustments
Prepare monthly inventory reports by pulling data and organizing to create monthly reports
Additional responsibilities as assigned supporting the AP team when needed

What we offer

Medical, vision, dental, and life and disability insurance
Eligibility to enroll in company 401(k) plan

Fulltime

Quality and Lean Specialist

We are on the lookout for a QA & Lean Specialist for our Rydalmare site. In this...

Location

Australia , Rydalmere

Salary:

Not provided

Hunter Douglas

Expiration Date

Until further notice

Requirements

Hands-on, technically minded professional with strong problem-solving skills and a passion for continuous improvement
Experience in quality and Lean practices in a production or warehouse environment
Ability to communicate clearly, lead by example, and influence at all levels
Thrive on driving efficiency, coaching teams, and delivering high standards every day

Job Responsibility

Lead and maintain quality control programs across fabrication and warehouse operations, ensuring adherence to internal standards and customer expectations
Analyse quality data, customer feedback, and production reports to identify trends, root causes, and improvement opportunities
Implement and champion Lean Manufacturing tools and techniques to streamline processes, reduce waste, and drive continuous improvement
Coach and upskill teams in problem solving, visual management, root cause analysis, and performance gap resolution
Collaborate with cross-functional teams to resolve supplier quality issues and ensure accurate procurement specifications
Oversee the non-conformance and dispensation processes, including documentation, investigation, and corrective actions
Coordinate calibration schedules for equipment and maintain quality assurance records and compliance documentation
Monitor delivery performance metrics and lead initiatives to improve order fulfilment accuracy and timeliness

What we offer

Access to Club Social – exclusive benefits and events
On-site parking for convenience and ease
Signature career development opportunities to help you grow professionally
Generous employee discount on our products
Be part of an amazing culture with strong collaboration across teams

Manufacturing Excellence Specialist

Nestle Health Science

Location:
United States , Eau Claire

Category:
Manufacturing

Contract Type:
Not provided

Salary:

Job Description:

Job Responsibility:

Requirements:

Additional Information:

Job Posted:
February 13, 2026

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Job Posted:February 13, 2026

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