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Summer 2027 Provider Delivery Software Engineer enGen Undergraduate Intern
Highmark Health
Jefferson City, MO
…experience developing enterprise-scale software solutions that support provider-focused digital products and services across the healthcare industry. This internship is designed to develop…
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Senior Data Engineering Specialist
Association of American Medical Colleges
Remote, United States
Provide technical leadership, coaching, and code reviews for junior engineers and peers to promote skill development and uphold engineering best practices.
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Instrument & Calibration Technician II
AstraZeneca Pharmaceuticals LP Company
Rockville, MD
· Support the maintenance of asset lifecycle records, instrument inventories, calibration histories, and associated technical documentation.
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Instrument & Calibration Technician III
AstraZeneca Pharmaceuticals LP Company
Rockville, MD
· Support the maintenance of asset lifecycle records, instrument inventories, calibration histories, and associated technical documentation.
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Senior Principal AI Research Engineer
Pfizer Inc
WA · CA · MA · CT · NY
- $139,100 to $231,900 USD / year
You'll work alongside experts in AI, engineering, computational biology, and drug discovery while taking on increasing technical ownership and influence.
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Senior AI Research Engineer
Pfizer Inc
WA · CA · MA · CT · NY
- $106,000 to $176,600 USD / year
You'll work alongside experts in AI, engineering, computational biology, and drug discovery while taking on increasing technical ownership and influence.
Added 2 mins ago
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Lead Industrial Construction Estimator
GPAC
Washington
- $160,000 to $200,000 USD / year
…pricing strategies, and collaborate with project management, engineering, procurement, and construction teams to support successful project execution and…
Added 2 mins ago
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Lead Industrial Construction Estimator
GPAC
Seattle, WA
- $160,000 to $200,000 USD / year
…pricing strategies, and collaborate with project management, engineering, procurement, and construction teams to support successful project execution and…
Added 2 mins ago
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Lead Industrial Construction Estimator
GPAC
Seattle, WA
- $160,000 to $200,000 USD / year
…pricing strategies, and collaborate with project management, engineering, procurement, and construction teams to support successful project execution and…
Added 2 mins ago
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Lead Industrial Construction Estimator
GPAC
Renton, WA
- $160,000 to $200,000 USD / year
…pricing strategies, and collaborate with project management, engineering, procurement, and construction teams to support successful project execution and…
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Lead Industrial Construction Estimator
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Tacoma, WA
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Lead Industrial Construction Estimator
GPAC
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- $160,000 to $200,000 USD / year
…pricing strategies, and collaborate with project management, engineering, procurement, and construction teams to support successful project execution and…
Added 2 mins ago
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Lead Industrial Construction Estimator
GPAC
Federal Way, WA
- $160,000 to $200,000 USD / year
…pricing strategies, and collaborate with project management, engineering, procurement, and construction teams to support successful project execution and…
Added 2 mins ago
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Lead Industrial Construction Estimator
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- $160,000 to $200,000 USD / year
…pricing strategies, and collaborate with project management, engineering, procurement, and construction teams to support successful project execution and…
Added 2 mins ago
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Lead Industrial Construction Estimator
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South Hill, WA
- $160,000 to $200,000 USD / year
…pricing strategies, and collaborate with project management, engineering, procurement, and construction teams to support successful project execution and…
Added 2 mins ago
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Lead Industrial Construction Estimator
GPAC
Sumner, WA
- $160,000 to $200,000 USD / year
…pricing strategies, and collaborate with project management, engineering, procurement, and construction teams to support successful project execution and…
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Principal Design Verification Engineer , Annapurna Labs
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Cupertino, CA
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Collaborate with internal teams, customers, and vendors to support the project lifecycle, including installations and the resolution of technical issues
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- $24 to $30 USD / hour
…high-pressure propellant systems. Working closely with welding engineering, manufacturing, and quality teams, you will follow qualified welding procedures, maintain strict cleanliness and…
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Supplier Development Engineer
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We are seeking a skilled and motivated Supplier Development Engineer to support the Ranger spacecraft program by ensuring the technical capability, quality, and performance of suppliers…
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Senior Cost Manager / Quantity Surveyor – Data Center Construction
Turner & Townsend
Van Wert, OH
Good knowledge of construction industry technical matters, such as different procurement routes, value management, and value engineering.
Added 4 mins ago
Senior Cost Manager / Quantity Surveyor – Data Center Construction
Turner & Townsend
Fort Wayne, IN
Good knowledge of construction industry technical matters, such as different procurement routes, value management, and value engineering.
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Applied AI Engineer Intern
Parspec
San Mateo, CA
We’re seeking an Applied AI Engineer Intern to join Parspec. This role is part of the AI team and works closely with Product and Engineering on fast-moving, real-world applications of AI.

Closed listing

Catalent

Supervisor - Engineering, Validation

Madison, WI, United States

This opening has closed.

The original listing is kept below for reference.

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Job details

Experience: 0–2 years of leadership experience required.
Posting language: English
Posted: Nov 6, 2026

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Original job description

Archived listing. The details below describe a past opening.

About Site Catalent’s Madison, Wisconsin site is a state‑of‑the‑art biologics development and manufacturing facility supporting customers from research through early‑ and mid‑stage clinical production. Located at 726 Heartland Trail in Madison, the approximately 102,700‑square‑foot GMP facility specializes in mammalian cell line engineering, drug substance biomanufacturing, and biopharmaceutical development, utilizing flexible single‑use systems to enable rapid scale‑up and customization. The site is home to Catalent’s proprietary GPEx® and GPEx® Lightning technologies, which are used to generate high‑yielding mammalian cell lines for biologic therapies, and supports production scales ranging from 50 to 4,000 liters for clinical manufacturing. Following a $45 million expansion announced in 2025, the Madison site has significantly increased capacity, added new equipment, and created approximately 200 highly skilled biohealth jobs, further strengthening its role within Catalent’s global biologics network and Wisconsin’s growing life sciences ecosystem.

Position Summary We have an opportunity for a Supervisor - Engineering, Validation to join our team in Madison, WI. This role supports the Quality Assurance department, ensuring compliance with FDA and other regulatory requirements. The position oversees validation programs, including commissioning, qualification, and computer system validation, while maintaining systems in a validated state. The Supervisor will lead a team of validation professionals, ensuring quality, compliance, and continuous improvement across all validation activities.

Shift: M-F 8am-5pm Location: Madison, WI 100% Onsite

The Role

Lead a team of Validation professionals.
Maintain Validation Master Plans.
Review and approve validation protocols and reports.
Support commissioning, qualification, and validation activities.
Review Change Controls.
Manage requalification programs.
Participate in audits and inspections.
Drive continuous improvement initiatives.
Serve as Validation Subject Matter Expert (SME).
Coordinate with Quality Assurance, Manufacturing, Facilities, Engineering, and customers.
Provide technical training and support.

The Candidate Minimum Requirements

Doctorate degree in a STEM field with at least 2 years of related experience, or Master’s degree in a STEM field with at least 4 years of related experience, or Bachelor’s degree in a STEM field with at least 5 years of related experience.
0–2 years of leadership experience required.
Experience in Commissioning, Qualification, and Validation (CQV).
Knowledge of validation lifecycle management.
Experience with Change Control impact assessments.
Experience in requalification and periodic reviews.
Proficiency in validation protocol and report writing and execution.
Strong understanding of current Good Manufacturing Practices (cGMP).
Knowledge of FDA, ICH, and EMA regulations.
Ability to interpret regulatory guidance and validation requirements.
Experience leading validation projects and initiatives.
Frequent sitting, standing, walking, computer work, and document review.
Occasional bending, kneeling, crouching, and carrying materials.
Frequent lifting up to 10 lbs and occasional lifting up to 50 lbs.
Ability to work within cleanroom environments as needed.

Preferred Skills & Background

Experience in pharmaceutical manufacturing.
Experience in biologics manufacturing.
Experience in biotech manufacturing.
Experience in cell therapy or gene therapy environments.
Experience in Contract Development and Manufacturing Organizations (CDMOs) such as Catalent, Thermo Fisher Scientific, AbbVie, Fujifilm Diosynth, Lonza, CSL Behring, Pfizer, Amgen, Lilly, or Genentech.
Experience supporting biologics operations involving manufacturing processes and validated systems.

Why You Should Join Catalent

Defined career path and annual performance review and feedback process.
Diverse, inclusive culture.
Potential for career growth on an expanding team within an organization dedicated to preserving and bettering lives.
Competitive paid time off plus 8 paid holidays.
Community engagement and green initiatives.
Medical, dental, and vision benefits effective day one of employment.
Tuition reimbursement.

Catalent offers rewarding opportunities to further your career! Join the global drug development and delivery leader and help us bring over 7,000 life-saving and life-enhancing products to patients around the world. Catalent is an exciting and growing international company where employees work directly with pharma, biopharma and consumer health companies of all sizes to advance new medicines from early development to clinical trials and to the market. Catalent produces more than 70 billion doses per year, and each one will be used by someone who is counting on us. Join us in making a difference.

personal initiative. dynamic pace. meaningful work. Visit Catalent Careers to explore career opportunities.

Catalent is an Equal Opportunity Employer, including disability and veterans.

If you require reasonable accommodation for any part of the application or hiring process due to a disability, you may submit your request by sending an email, and confirming your request for an accommodation and include the job number, title and location to DisabilityAccommodations@catalent.com. This option is reserved for individuals who require accommodation due to a disability. Information received will be processed by a U.S. Catalent employee and then routed to a local recruiter who will provide assistance to ensure appropriate consideration in the application or hiring process.

Notice to Agency and Search Firm Representatives: Catalent Pharma Solutions (Catalent) is not accepting unsolicited resumes from agencies and/or search firms for this job posting. Resumes submitted to any Catalent employee by a third party agency and/or search firm without a valid written & signed search agreement, will become the sole property of Catalent. No fee will be paid if a candidate is hired for this position as a result of an unsolicited agency or search firm referral. Thank you.

Important Security Notice to U.S. Job Seekers: Catalent NEVER asks candidates to provide any type of payment, bank details, photocopies of identification, social security number or other highly sensitive personal information during the offer process, and we NEVER do so via email or social media. If you receive any such request, DO NOT respond - it is a fraudulent request. Please forward such requests to spam@catalent.com for us to investigate with local authorities.

California Job Seekers can find our California Job Applicant Notice HERE.

Volunteer Work Disclosure: Applicants for employment in Massachusetts may include in their employment history any verified work performed on a volunteer basis.

Massachusetts Lie Detector Test Notice: It is unlawful in Massachusetts to require or administer a lie detector test as a condition of employment or continued employment. An employer who violates this law may be subject to criminal penalties and civil liability. Consistent with Massachusetts law, Catalent does not require or administer lie detector tests as a condition of employment or continued employment.

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Skills

Quality assurance
Regulatory compliance
Lead a team
Process improvement
Inspection
Provide technical training
Leadership
Report writing
Good manufacturing practices
Heavy lifting
Pharmaceutical processes
Manufacturing processes
Community engagement

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