Kindeva Drug Delivery

Sr. Manager, Manufacturing Engineering

Kindeva Drug Delivery  •  Lexington, KY (Onsite)  •  8 days ago
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Job Description

Our Work Matters
At Kindeva, we make products that save lives, ensuring better health and well-being for patients around the world.
Why Kindeva?
• Purpose-driven work environment
• Significant growth potential
• Collaborative team culture
• Direct impact on patient care
• Industry-leading innovation
At Kindeva, we make products that save lives, ensuring better health and well-being for patients around the world.
The Impact You Will Make: The Engineering Manager will be responsible for building and administering a comprehensive capital spend program, managing high-impact capital projects, and leading the Engineering staff at the Kindeva Lexington manufacturing facility.
This role requires a strong background in CGMP manufacturing, automation, facility design, commissioning, and qualification to ISO cleanroom guidelines.
The Engineering Manager will ensure the successful execution of capital projects that support the company's strategic goals, driving efficiency, compliance, and innovation in facility operations.

ROLE RESPONSIBILITIES
Capital Spend Program Management:
• Develop, implement, and oversee a capital spend program, aligning with the company’s strategic objectives and budgetary constraints.
• Monitor capital expenditures and ensure efficient allocation of resources across multiple projects.
• Provide regular updates to senior management on capital spend, project status, and potential risks or opportunities.
• Project Management:
• Lead the planning, design, and execution of high-impact capital projects, ensuring adherence to timelines, budgets, and quality standards.
• Collaborate with cross-functional teams, including manufacturing, quality, and regulatory, to ensure projects meet CGMP and ISO requirements.
• Manage project teams, including internal staff, contractors, and vendors, to deliver projects on time and within scope.
• Oversee the commissioning, qualification, and validation of new equipment and facilities, ensuring compliance with regulatory standards.

Automation and Technology Integration:
• Drive the implementation of automation technologies to improve manufacturing efficiency, reduce downtime, and enhance product quality.
• Evaluate and select automation solutions that align with the company’s manufacturing needs and regulatory requirements.
• Ensure seamless integration of automation systems with existing processes and infrastructure.
• Regulatory Compliance and Quality Assurance:
• Develop and enforce standard operating procedures (SOPs) and best practices for engineering activities.
• Support internal and external audits, providing documentation and addressing any findings related to engineering projects.
• Team Leadership and Development:

Leadership:
• Manage and mentor a team of engineers and technical staff, fostering a culture of continuous improvement and professional growth.
• Identify training needs and provide opportunities for staff to enhance their skills and knowledge in relevant areas.
• Promote a safety-first culture by ensuring all engineering activities adhere to safety regulations and protocols.

BASIC QUALIFICATIONS
• BASIC QUALIFICATIONS
• Bachelor’s degree in engineering (Mechanical, Electrical, Chemical, or related field). Advanced degree preferred.
• 15+ years of experience in engineering roles, with a focus on capital projects in a pharmaceutical manufacturing environment.
• Proven experience in managing large-scale capital projects, including budgeting, scheduling, and resource allocation.
• Strong knowledge of CGMP regulations, FDA requirements, and ISO cleanroom guidelines.
• Background in automation technologies and their application in manufacturing processes.
• Excellent project management skills, including the ability to lead cross-functional teams and manage multiple projects simultaneously.
• Bachelor’s degree in engineering (Mechanical, Electrical, Chemical, or related field). Advanced degree preferred.
• Background in automation technologies and their application in manufacturing processes.
• Excellent project management skills, including the ability to lead cross-functional teams and manage multiple projects simultaneously.
• Strong problem-solving, decision-making, and leadership abilities.
• Effective communication and interpersonal skills.
• Preferred Skills:
• Certification in Project Management (PMP) or related disciplines.
• Experience with pharmaceutical facility design and construction.
• Familiarity with lean manufacturing principles and continuous improvement methodologies.
• Proficiency with project management software
• Problem-solving, decision-making, and leadership abilities.
• Effective communication and interpersonal skills.

PREFERRED SKILLS
• Certification in Project Management (PMP) or related disciplines.
• Experience with pharmaceutical facility design and construction.
• Familiarity with lean manufacturing principles and continuous improvement methodologies.
• Proficiency with project management software

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California residents should review our Notice for California Employees and Applicants before applying.

Kindeva does not accept unsolicited assistance from headhunters or recruitment firms for any of our job openings. Any resumes or candidate profiles submitted to Kindeva employees—regardless of format—without a valid, signed agreement and an approved job order from an authorized signatory in Talent Acquisition will be considered the sole property of Kindeva. No fees will be paid in the event that a candidate is hired as a result of an unsolicited resume or referral.

Equal Opportunity Employer:

Kindeva Drug Delivery is an Equal Opportunity/Affirmative Action Employer and does not discriminate on the basis of race, color, religion, gender, age, national origin, disability, Protected Veteran status, sexual orientation, or any other characteristic protected by federal, state or local law.

Do you see yourself as part of the Kindeva mission? Click Apply Now Today!
Kindeva Drug Delivery

About Kindeva Drug Delivery

Kindeva is a purpose-fueled, people-centric CDMO dedicated to advancing your project, your ambitions, and our industry. With a legacy of innovation and deep expertise in complex drug development, we serve as a trusted partner to pharmaceutical companies worldwide.

For us, fast-tracking healthier tomorrows starts with industry-leading finished-dose expertise. From early-stage formulation to full-scale commercial production, we optimize every step to help bring life-changing therapies to patients faster.

Built on a rich heritage of regulatory diligence and blockbuster devices, our expertise sharpens, optimizes, and maximizes your project—combining best-in-class facilities with specialist capabilities in injectable, inhalation, and dermal delivery, to ensure exceptional-by-design solutions throughout.

Strategically minded and dedicated to your lasting legacy, we provide value beyond manufacturing, turning your long-term possibilities into achievable milestones.

Because every patient deserves tomorrow.

For more information about how we can transform tomorrows together, please visit www.kindevadd.com.

Industry
Chemicals & Materials
Company Size
1,001-5,000 employees
Headquarters
Woodbury, Minnesota
Year Founded
2020
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