Science & Research H-1B Sponsorship Jobs in Kentucky

Senior Manager, Production

About Site

Catalent’s Winchester, KY site is the company’s flagship U.S. manufacturing location for large‑scale oral solid dose forms, operating from a 180,000‑square‑foot facility with fully integrated development and analytical services. The site specializes in complex and controlled‑release oral dose technologies, supporting product development, technology transfer, and commercial manufacturing across pharmaceutical and consumer health programs. Winchester has a long commercial manufacturing track record, having launched 100+ products and producing billions of tablets and capsules annually, making it a critical site within Catalent’s oral dose network.

Position Summary

We have an opportunity for a Senior Manager, Production to join our team and lead operations to deliver high-quality products on time and within budget. This role ensures compliance with cGMP standards, safety regulations, and operational excellence. You will manage departmental success through strategic leadership, collaboration, and continuous improvement. This position plays a key role in driving performance, efficiency, and innovation within the manufacturing environment.

Shift: Monday - Friday 8 AM - 5 PM

Location: Winchester, KY

100% Onsite

The Role

• Oversee daily performance against established standards and schedules, resolving workflow and technical issues to support 24/7 operations.
• Liaise with support functions to ensure efficient schedules and quality products, managing material, staff, and information flow.
• Interface with Materials Management and warehouse staff on raw material inventory control issues.
• Collaborate across functions to achieve shared goals.
• Ensure compliance with cGMP and safety regulations within the Manufacturing department.
• Maintain the facility in a “tour ready” state, ensuring proper flow, cleaning, and zone concepts.
• Manage audits, corrective action plans, and interactions with governmental agencies and customers.
• Ensure operators are trained and follow standard operating procedures and regulations.
• Verify batch records are complete and accurate the first time.
• Work with process development and customers for process scale-up and optimization.
• Troubleshoot processing, equipment, or utility issues.
• Define and implement Corrective/Preventive Action measures for audits and deviations, meeting commitments on time.
• Promote Operational Excellence, Six Sigma, and Lean methodologies, including running Kaizen Events.
• Provide technical expertise during development of new manufacturing platforms and products.
• Manage screening, hiring, training, evaluation, and development of operations staff.
• Recruit and develop top talent, fostering engagement and a culture of continuous improvement.
• Oversee activities of Supervisors and material expeditors, providing guidance as needed.
• Identify and maintain staffing needs, working with HR and training teams to build a skilled workforce.
• Make personnel recommendations on staffing, wages, and performance reviews.
• Manage manufacturing staff deployment, including selection, evaluation, and grievance resolution.
• Assist in developing strategic operational plans.
• Participate in managing the P&L impact of operations, including cost center spending, headcount, and budgeting.
• Perform other duties as required to support high performance.

The Candidate

Minimum Requirements

• Bachelor’s degree and 3 years of prior supervisory or relevant management experience.
• Ability to create and work within an operating plan framework and budget.
• Thorough knowledge of equipment and processes used in the facility and within the pharmaceutical industry.
• Strong understanding of cGMP, FDA, and DEA guidelines and their application.
• Knowledge of Solid Dosage manufacturing.
• Excellent computer skills.
• Ability to manage priorities and projects effectively, with strong communication and people management skills.
• Skills in diplomacy, negotiation, team building, independent work, coaching, and delegation.
• Capability to work in a matrix organization and think systematically.
• Proficient in English verbal and written communication, with excellent presentation skills.
• Proficient in Microsoft Office applications (Word, Excel, PowerPoint).
• Ability to work effectively under pressure to meet deadlines.
• Individual may be required to sit, stand, or walk for extended periods.
• Specific vision requirements include reading written documents and frequent use of a computer monitor.
• Demonstrable leadership experience at Catalent (including but not limited to participation in Catalent-sponsored leadership programs such as NGGL, GOLD, LEAD Now, GM Excellence, and GROW) may be considered in place of external experience.

Preferred Skills & Background

• Experience in pharmaceutical or biotech manufacturing.
• Operational excellence certification preferred.

Why You Should Join Catalent

• Positive and fast-paced working environment focused on continuous improvement and innovation.
• Competitive Paid Time Off plus 8 paid holidays.
• Medical, dental, and vision benefits effective day one of employment.
• Tuition Reimbursement to help you finish your degree or earn a new one.
• Engaging site-based activities such as NCAA Basketball Brackets, Golf Scrambles, and Annual Onsite Pet Adoption Events.
• Employee Resource Groups promoting Diversity and Inclusion.
• Green initiatives and community engagement, including Adopt-a-Highway Clean-up.
• Defined career path with annual performance reviews and growth opportunities.
• WellHub program supporting physical and mental wellness.
• Exclusive discounts through Perkspot from over 900 merchants.

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.

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.