Top 37 Manufacturing equipment validation engineer Jobs in Akron Oh

Manufacturing Equipment Validation Engineer
Hikma Pharmaceuticals —Bedford, OH
- $59,900 - $120,450 a year
- Full-time
- Engineering
- Master's degree
- Supervising experience
- Paid parental leave
- Paid holidays
Quick Apply
11d
ENGINEER ELECTRICAL SR
The Will-Burt Company —Orrville, OH
- $80,459.80 - $96,897.82 a year
- Full-time
- Background check
- Customer service
- 5 years
- Profit sharing
- Health insurance
Quick Apply
4d
Senior Validation Engineer
Hikma Pharmaceuticals —Bedford, OH
- $56,950 - $95,000 a year
- Full-time
- Ability to walk for extended periods
- Bachelor of Science
- Research
- Paid parental leave
- Paid holidays
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Maintenance Engineer
Hikma Pharmaceuticals —Bedford, OH
- $59,900 - $120,450 a year
- Full-time
- Microsoft Excel
- Microsoft Outlook
- OSHA
- Paid parental leave
- Health savings account
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Automation Engineer
Hikma Pharmaceuticals —Bedford, OH
- $59,900 - $120,450 a year
- Full-time
- Microsoft Word
- Microsoft Excel
- Research
- Paid parental leave
- Paid holidays
Quick Apply
Manufacturing Process Engineer
LG Chem —Akron, OH
- Monday to Friday
- Microsoft Excel
- Microsoft Outlook
- Bachelor of Science
Manufacturing Engineer
Röchling SE & Co. KG —Akron, OH
- Full-time
- Mid-level
- 3 years
- Health savings account
- Health insurance
Senior / Staff Manufacturing Equipment Engineer - Hydraulic Hose
Continental —Fairlawn, OH
- Online Application
- Hybrid work
- 5 years
- English
- Assembly
- Disability insurance
Manufacturing Engineer
Rockwell Automation —Twinsburg, OH
- Full-time
- Mid-level
- Office
- Assembly
- Health insurance
- Dental insurance
Manufacturing Engineer - Automation
Continental Group Sector ContiTech —Fairlawn, OH
- Full-time
- Hybrid work
- 7 years
- Engineering
- English
Quick Apply
4d
Engineering Co-Op
Performance Health Supply,LLC —Akron, OH
- $20 an hour
- Seasonal
- High school diploma or GED
- Analysis skills
- Internship
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Engineering Co-Op
Performance Health —Akron, OH
- $20 an hour
- Full-time
- High school diploma or GED
- Communication skills
- Mechanical knowledge
Sr. Validation Engineer
Hikma Pharmaceuticals PLC —Bedford, OH
- $59,900 - $120,450 a year
- Full-time
- Ability to walk for extended periods
- Bachelor of Science
- Research
- Paid parental leave
- Paid holidays
Fall Engineering Co-Op
Parker Hannifin Corporation —Akron, OH
- Customer service
- Electrical Engineering
- Entry level
3d
Equipment Validation Supervisor
Hikma Pharmaceuticals PLC —Bedford, OH
- $59,900 - $120,450 a year
- Full-time
- Engineering
- Master's degree
- Supervising experience
- Paid parental leave
- Paid holidays
10d
Project Engineer – Controls & Electrical
Americhem —Cuyahoga Falls, OH
- Engineering
- System design
- Mid-level
Quick Apply
Automation Engineer
Hikma Pharmaceuticals PLC —Bedford, OH
- $59,900 - $120,450 a year
- Full-time
- Microsoft Word
- Microsoft Excel
- Research
- Paid parental leave
- Paid holidays
Controls Engineer
Rockwell Automation —Twinsburg, OH
- Full-time
- System design
- Mid-level
- Continuous improvement
- Health insurance
- Dental insurance
Surface Mount Technology (SMT) Lead Engineer
CEIA USA —Hudson, OH
- Full-time
- 6 years
- Engineering
- Office
- Profit sharing
- Paid training
Quick Apply
Machining Process Engineer
NMG Aerospace —Stow, OH
- 5 years
- Engineering
- ERP systems
- Health insurance
- Paid time off
Quick Apply

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manufacturing equipment validation engineer jobs near akron oh

Manufacturing Equipment Validation Engineer

Hikma Pharmaceuticals
Bedford, OH

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Job Details

Full-time
$59,900 - $120,450 a year
11 days ago

Benefits

Paid parental leave
Paid holidays
Disability insurance
Health insurance
Dental insurance
401(k)
Tuition reimbursement
Paid time off
Parental leave
Vision insurance
401(k) matching
Employee discount
Life insurance
Prescription drug insurance

Qualifications

Teamwork
Team leadership
Master's degree
Manufacturing facility experience
Supervising experience
Lean Six Sigma
Stakeholder relationship building
FDA regulations
Stakeholder management

Full Job Description

Job Title: Equipment Validation Supervisor

Location: Bedford, Ohio

Job Type: Full-Time

Req ID: 11863

About Us:

As a developer, manufacturer, and supplier of essential medicines, Hikma Pharmaceuticals USA Inc. and its affiliates’ mission is to bring Better Health. Within Reach. Every Day.® for millions of patients around the world. We are a trusted, reliable partner and dependable source of over 800 high-quality generic, specialty and branded pharmaceutical products that hospitals, physicians and pharmacists need to treat their patients across North America, the Middle East, North Africa and Europe. Through our 32 manufacturing plants, eight R&D centers, and 9,500+ employees worldwide, we are always hard at work creating high-quality medicines and making them accessible to the people who need them.

Description:

We are committed to building a diverse and inclusive team and encourage applications from candidates of all backgrounds. We are seeking a talented and motivated Equipment Validation Supervisor to join our team. In this role, you will be responsible for leading equipment qualification and validation activities across manufacturing and laboratory systems, with a strong focus on sterile and injectable product environments. This role ensures compliance with FDA, cGMP, and global regulatory standards, while supporting Hikma’s commitment to high-quality, accessible medicines.

The Supervisor will manage a team of validation professionals, oversee IQ/OQ/PQ activities, and collaborate cross-functionally to support new product introductions, capacity expansion, and continuous improvement initiatives.

Key Responsibilities:

Leadership & Team Management

Lead, coach, and develop a team of validation engineers/specialists.
Allocate resources and manage validation priorities aligned with production and project timelines.
Foster a culture of compliance, quality, and continuous improvement.

Equipment Qualification & Validation

Oversee and approve execution of:
Installation Qualification (IQ)
Operational Qualification (OQ)
Performance Qualification (PQ)
Ensure validation of critical GMP equipment, including:
Filling lines, autoclaves, lyophilizers, sterilizers
HVAC systems and cleanroom equipment
Packaging and inspection systems
Ensure compliance with Annex 1 (sterile manufacturing) where applicable.

Regulatory Compliance & Quality

Ensure all validation activities comply with:
FDA (21 CFR Part 210/211)
EU GMP / Annex 1
ICH guidelines
Maintain inspection readiness for FDA, MHRA, and other global regulatory audits.
Review and approve validation protocols, reports, SOPs, and change controls.

Project & Lifecycle Management

Lead validation efforts for:
New equipment and facility expansions
Technology transfers and new product launches
Manage equipment lifecycle, including periodic review and requalification.
Collaborate with Engineering and Manufacturing on commissioning and qualification (C&Q).

Deviation, CAPA & Risk Management

Oversee investigations related to validation failures or deviations.
Lead root cause analysis and ensure timely implementation of CAPA.
Conduct risk assessments using tools like FMEA and support risk-based validation strategies.

Cross-functional Collaboration

Partner with QA, Engineering, MS&T, Regulatory Affairs, and Operations teams.
Support process improvements and operational efficiency initiatives.
Provide technical expertise during audits, inspections, and regulatory submissions.

Qualifications & Experience

We value the skills and experiences candidates bring to the table. While we have listed some qualifications below, we encourage candidates to apply even if they do not meet all of them:

Education

Bachelor’s degree in Engineering, Pharmaceutical Sciences, Life Sciences, or related discipline
Master’s degree preferred

Experience

5+ years of experience in pharmaceutical validation, preferably in sterile/injectable manufacturing
Minimum 1 year in a supervisory or leadership role
Experience working in FDA-inspected facilities

Technical Expertise

Deep knowledge of validation lifecycle (IQ/OQ/PQ) and risk-based validation approaches
Strong experience with aseptic processing and sterile equipment validation
Familiarity with:
GAMP 5 (for computerized systems)
Cleaning validation and process validation (preferred)
Understanding of calibration, maintenance, and asset lifecycle systems

Soft Skills

Strong leadership and team development skills
Excellent communication and stakeholder management
High attention to detail and strong documentation skills
Ability to manage multiple priorities in a fast-paced GMP environment

Preferred Qualifications

Experience in injectables or high-volume generics manufacturing
Lean Six Sigma certification
Experience with electronic validation systems and QMS platforms (e.g., TrackWise, Veeva)

What We Offer*:

Annual performance bonus, commission, and share potential
Auto enrollment in a Hikma-sponsored 401(k) program at a pre-tax contribution rate of 4% of eligible pay. Hikma will match 100% of the first 6% of eligible pay that you contribute
A generous paid time off (PTO) bank starting with 20 days (prorated based on hire date). Additional days granted upon reaching work milestone anniversaries
3 personal days (prorated based on hire date)
11 company paid holidays
Comprehensive benefits including health, dental, vision, mental health, disability, life insurance, prescription drug coverage, and a variety of voluntary benefits
Employee discount program
Wellbeing rewards program
Safety and Quality is a top organizational priority
Career advancement and growth opportunities
Tuition reimbursement
Paid maternity and parental leave

*Eligibility requirements apply to some benefits and depend on the job classification, role, and length of employment. Benefits are subject to change as well as specific plan or program terms.

Recruiters:

Please note that Hikma has a set roster of approved recruiters for specific roles agreed to in advance and does not accept unsolicited resumes or calls from third-party recruiters or employment agencies regarding open positions. In the absence of a signed agreement and approval from Hikma’s Human Resources department to submit resumes for a specific position, Hikma will not approve, nor will be under an obligation to make, any payment to such non-approved third-parties in the event a candidate they refer is hired by Hikma.

Equal Opportunity Employer:

Hikma Pharmaceuticals USA Inc. is an Equal Opportunity Employer. Employment decisions are made without regard to race, color, religion, national or ethnic origin, sex, sexual orientation, gender identity or expression, age, disability, protected veteran status, or other characteristics protected by law.

Pay: $59,900.00 - $120,450.00 per year

Benefits:

401(k)
401(k) matching
Employee discount
Health insurance
Life insurance
Paid time off

Work Location: In person

Quick Apply

Refine Your Search

manufacturing equipment validation engineer jobs in akron oh

Manufacturing Equipment Validation Engineer

ENGINEER ELECTRICAL SR

Senior Validation Engineer

Maintenance Engineer

Automation Engineer

Manufacturing Process Engineer

Manufacturing Engineer

Senior / Staff Manufacturing Equipment Engineer - Hydraulic Hose

Manufacturing Engineer

Manufacturing Engineer - Automation

Engineering Co-Op

Engineering Co-Op

Sr. Validation Engineer

Fall Engineering Co-Op

Equipment Validation Supervisor

Project Engineer – Controls & Electrical

Automation Engineer

Controls Engineer

Surface Mount Technology (SMT) Lead Engineer

Machining Process Engineer

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