Top 38 Manufacturing specialist Jobs in Delaware, Oh

Manufacturing Specialist-Process Engineer
Amgen —New Albany, OH
- $107,545.40 - $145,502.60 a year
- Doctoral degree
- Mid-level
- Master's degree
- Disability insurance
- Health insurance
Production Specialist Operator - 3rd shift
Abbott Laboratories —Columbus, OH
- $19.05 - $38.15 an hour
- Full-time
- Forklift
- High school diploma or GED
- Children
- Paid holidays
- Health insurance
Transaction Specialist I- Print Operator
JPMorganChase —Westerville, OH
- Full-time
- Ability to walk for extended periods
- 5 years
- High school diploma or GED
- Health insurance
- Tuition reimbursement
Tech Service Specialist - Lamination Adhesives Job
Arkema B.V. —Dublin, OH
- $70,000 - $90,000 a year
- Monday to Friday
- Customer service
- Mid-level
- Bachelor's degree
- Health insurance
- Benefits from day one
Product Specialist – Manufacturing
Vertiv —Westerville, OH
- Oracle
- 3 years
- Analysis skills
QA Change Control Specialist II
American Regent, Inc. —New Albany, OH
- Overtime
- Microsoft Excel
- Mid-level
- Office
Specialist I, QA Operations
Forge Biologics —Columbus, OH
- Full-time
- Microsoft Excel
- Microsoft Outlook
- Mid-level
- Paid parental leave
- Disability insurance
Quick Apply
10d
Principal Specialist, Quality Assurance - Microbiology
Cardinal Health —Lewis Center, OH
- $80,900 - $103,950 a year
- Bachelor's degree
- No degree
- Mentoring
- Paid parental leave
- Health savings account
Characterization Process Development Specialist
Validation & Engineering Group, Inc —New Albany, OH
- Full-time
- Organizational skills
- Senior level
- Communication skills
Quick Apply
7d
Operations Technical Training Specialist
Vertiv —Delaware, OH
- Mid-level
- Office
- Analysis skills
- On-the-job training
Tech Service Specialist - Lamination Adhesives Job
Arkema —Dublin, OH
- $70,000 - $90,000 a year
- Monday to Friday
- Customer service
- Mid-level
- Bachelor's degree
- Health insurance
- Benefits from day one
Specialist II, QA Complaints
Hikma Pharmaceuticals PLC —Columbus, OH
- Full-time
- Microsoft Excel
- Microsoft Outlook
- Engineering
- Paid parental leave
- Paid holidays
9d
Quality Assurance Specialist - Complaints
BI Pharmaceuticals, Inc. —Columbus, OH
- Full-time
- Hybrid work
- Microsoft Word
- 7 years
- Microsoft Excel
JR. Automation Specialist
CITYWIDE RX LLC —Columbus, OH
- $23 - $25 an hour
- Full-time
- Computer skills
- Communication skills
- Entry level
- Paid training
- Paid holidays
Quick Apply
11d
Specialist Production
Versiti, Inc. —Columbus, OH
- Full-time
- Microsoft Excel
- Microsoft Outlook
- Customer service
- Paid holidays
- Disability insurance
Quality Assurance Validation Specialist
Eliquent Life Sciences, Inc —Columbus, OH
- $100,000 a year
- Computer Science
- Engineering
- Mid-level
- Health insurance
- Dental insurance
Quick Apply
3d
Embroidery Specialist
Leader Promotions Inc —Columbus, OH
- High school diploma or GED
- 1 year
- Entry level
- Paid holidays
- Paid time off
Quick Apply
Senior Quality Assurance Specialist - Investigations
Andelyn Biosciences, Inc —Columbus, OH
- Full-time
- Microsoft Excel
- Bachelor's degree
- Continuous improvement
- Paid parental leave
- Paid holidays
Quick Apply
5d
QA Technical Services Specialist III
American Regent, Inc. —New Albany, OH
- Full-time
- 5 years
- Bachelor of Science
- Analysis skills
Commissioning / Qualification / Validation Specialist
Salas O'Brien, Inc. —Columbus, OH
- $90,000 - $100,000 a year
- Hybrid work
- Microsoft Excel
- 5 years
- Data analysis skills
- Paid holidays
- Health insurance
14d

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Manufacturing Specialist-Process Engineer

Amgen -
New Albany, OH

Apply Now

Job Details

$107,545.40 - $145,502.60 a year

Benefits

Disability insurance
Health insurance
Dental insurance
Flexible spending account
Vision insurance
Retirement plan

Qualifications

Incident investigation techniques for hazard identification
Performance monitoring
New product introduction
Operational analysis
Performance improvement leadership
Content creation for technical audiences
Production data analysis
Defect resolution root cause analysis
Doctoral degree
Project management experience in technology
Document control experience within pharmaceutical industry
Quality control statistical data analysis
Pharmaceutical regulatory compliance
Preventive action implementation
Triage
Statistical Process Control
Technical writing experience within manufacturing
Production deviation management
Six Sigma methodology implementation
Production risk assessment
Engineering process optimization
Corrective and preventive actions (CAPA)
Training material drafting
Mid-level
Project management experience in manufacturing
Trend analysis
Data summary reports
Master's degree
Quality reports
High school diploma or GED

Full Job Description

US - Ohio - New Albany

JOB ID: R-250262 LOCATION: US - Ohio - New Albany WORK LOCATION TYPE: On Site DATE POSTED: Aug. 21, 2026 CATEGORY: Manufacturing SALARY RANGE: 107,545.40USD -145,502.60 USD

Job Description

Join Amgen’s Mission of Serving Patients

At Amgen, if you feel like you’re part of something bigger, it’s because you are. Our shared mission—to serve patients living with serious illnesses—drives all that we do.

Since 1980, we’ve helped pioneer the world of biotech in our fight against the world’s toughest diseases. With our focus on four therapeutic areas –Oncology, Inflammation, General Medicine, and Rare Disease– we reach millions of patients each year. Amgen is advancing a broad and deep pipeline of medicines to treat cancer, heart disease, inflammatory conditions, rare diseases, and obesity and obesity-related conditions. As a member of the Amgen team, you’ll help make a lasting impact on the lives of patients as we research, manufacture, and deliver innovative medicines to help people live longer, fuller happier lives.

Our award-winning culture is collaborative, innovative, and science based. If you have a passion for challenges and the opportunities that lay within them, you’ll thrive as part of the Amgen team. Join us and transform the lives of patients while transforming your career.

Specialist, Manufacturing

What you will do

Let’s do this. Let’s change the world. This role will support the execution of manufacturing/quality systems such as continuous improvement, technology transfer / new product introductions, process validation, manufacturing process/procedures, risk assessments, training, and non-conformance. They will apply process, operational, scientific expertise, basic compliance knowledge, and analytical and troubleshooting skills to support operations. You may also serve as the primary production process owner for process support systems and assist with process ownership responsibilities on process systems.

Responsibilities may include, but are not limited to:

Applied Process Expertise

As a document owner, initiate, revise, and approve manufacturing procedures to ensure all procedures reflect current operations. Assess process performance by; observation of floor operations, review of performance data and provide troubleshooting support. Evaluate, plan, and implement solutions for process improvement opportunities. Assist in generation of training materials and / or in providing training on scientific or technical aspects of the process. Complete risk evaluations for new processes or changes to existing processes and issue the summary reports of these evaluations.

Projects and Initiatives

Bring continuous improvement initiatives for cost reduction or cycle time reduction and participate in the assessment or implementation of such special projects or initiatives.

Process Monitoring

Support process monitoring parameters and control limits based off critical metrics and recommend improvements. Collect process-monitoring data and support the assessment of deviations. Provide support of timely process monitoring quarterly reports.

Technology Transfer / New Product Introductions & Process or Equipment Modifications

Participate in technology transfer / NPI process to assess requirements for documentation, materials, training, and equipment modifications. Assess, prioritize, justify, and provide implementation and project management support for process or equipment modification projects.

Non-Conformance and CAPA

Ensure that all Non-conformance are triage within the established goal. Assist with investigations, corrective actions and NC/CAPA closure within established goal. Monitor and communicate incidents trends. Review equipment/system Root Cause Analysis investigations and support trend evaluations.

Process Validation

Assist with the process validation and generation of process validation protocols and reports. Support collection and analysis of process validation data.

Regulatory

May participate in regulatory inspections.

Change Control

As manufacturing change owner, provide assessments on CCRB records impacting the process.

What we expect of you

We are all different, yet we all use our outstanding contributions to serve patients. The professional we seek will possess these qualifications.

Basic Qualifications:

Doctorate degree

Or

Master’s degree and 2 years in Engineering, Manufacturing, Packaging or Quality experience in pharmaceutical, medical device or biotechnology companies.

Or

Bachelor’s degree and 4 years in Engineering, Manufacturing, Packaging or Quality experience in pharmaceutical, medical device or biotechnology companies.

Or

Associate’s degree and 8 years in Engineering, Manufacturing, Packaging or Quality experience in pharmaceutical, medical device or biotechnology companies.

Or

High school diploma / GED and 10 years in Engineering, Manufacturing, Packaging or Quality experience in pharmaceutical, medical device or biotechnology companies.

Preferred Qualifications:

Detailed technical understanding of bio-processing and manufacturing operations
Develop, manage, and implement process improvements
Experience with Lean principals (Kaizen, Six Sigma, Operational Excellence) and knowledge of problem-solving techniques
Experience in participating and helping lead cross-functional teams
Collaborate with staff at all levels in the organization, including technical and management staff within manufacturing, process development, and quality
Experience with change control process and change management
Skilled in performance of GMP production operations
Regulatory knowledge and interactions
Project management skills
Excellent organizational, technical writing, presentation, and verbal skills
Knowledge of data analysis and control charting

What you can expect of us

As we work to develop treatments that take care of others, we also work to care for your professional and personal growth and well-being. From our competitive benefits to our collaborative culture, we’ll support your journey every step of the way.

In addition to the base salary, Amgen offers a Total Rewards Plan, based on eligibility, comprising of health and welfare plans for staff and eligible dependents, financial plans with opportunities to save towards retirement or other goals, work/life balance, and career development opportunities that may include:

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, or for field sales representatives, a sales-based incentive plan
Stock-based long-term incentives
Award-winning time-off plans
Flexible work models where possible. Refer to the Work Location Type in the job posting to see if this applies.

and make a lasting impact with the Amgen team.

careers.amgen.com

In any materials you submit, you may redact or remove age-identifying information such as age, date of birth, or dates of school attendance or graduation. You will not be penalized for redacting or removing this information.

Sponsorship

Sponsorship for this role is not guaranteed.

As an organization dedicated to improving the quality of life for people around the world, Amgen fosters an inclusive environment of diverse, ethical, committed and highly accomplished people who respect each other and live the Amgen values to continue advancing science to serve patients. Together, we compete in the fight against serious disease.

Amgen is an Equal Opportunity employer and will consider all qualified applicants for employment without regard to race, color, religion, sex, sexual orientation, gender identity, national origin, protected veteran status, disability status, or any other basis protected by applicable law.

We will ensure that individuals with disabilities are provided reasonable accommodation to participate in the job application or interview process, to perform essential job functions, and to receive other benefits and privileges of employment. Please contact us to request accommodation.

Apply Now

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