Manufacturing Technician - Third Shift at Kindeva Drug Delivery

Lexington, Kentucky, United States -

Full Time

Start Date

Immediate

Expiry Date

03 Mar, 26

Salary

0.0

Posted On

03 Dec, 25

Experience

0 year(s) or above

Remote Job

Yes

Telecommute

Yes

Sponsor Visa

Skills

Manufacturing, Aseptic Technique, Sterilization Processes, Documentation, Team Collaboration, cGMP Compliance, Safety Protocols, Equipment Operation, Process Improvement, Training, Interpersonal Skills, Material Handling, Validation Protocols, Cleaning, Sanitizing, Maintenance

Industry

Pharmaceutical Manufacturing

Description

Our Work Matters At Kindeva, we make products that save lives, ensuring better health and well-being for patients around the world. The Impact You Will Make: If you are ready to work for a purpose, join Kindeva Drug Delivery! Working on the KDD Manufacturing Team as a Manufacturing Technician, you will play a crucial role in supporting the manufacturing of life-changing and life-saving prescription nasal spray medications. The Lexington location is experiencing exponential growth. Join our team, learn our processes, and grow with our organization. Together, as One Team, we will manufacture more tomorrows! Responsibilities: Responsibilities include cleaning, sanitizing, operating, and maintaining process equipment used to manufacture sterile nasal spray drug products and completing the associated documentation. By collaborating with cross-functional teams, you'll directly contribute to the improvement in patient outcomes around the world. Key Manufacturing Duties: Operate and monitor production equipment following PBRs and SOPs Clean and maintain manufacturing areas, equipment, and facilities Complete and review production documentation, including batch records and logbooks Train team members and coordinate with other departments Assist with validation protocols and improvement projects. Lead improvement projects and identify cost-saving opportunities Ensure compliance with cGMPs, SOPs, and safety protocols Qualifications: High School diploma or GED. 0 - 5 years of applicable experience working in a pharmaceutical manufacturing environment. Experience with sterilization processes or aseptic technique preferred. Good written communication skills to write SOPs and other cGMP documents. Qualified to work with controlled substances. Strong interpersonal skills and the ability to work well in a team environment. Physical Requirements: Regular use of hands for documentation, equipment operation, and material handling Extended periods of standing and walking Ability to lift/move up to 60 pounds occasionally Full range of vision capabilities (close, distance, color, peripheral, depth) Must wear required PPE and follow cGMP/safety procedures Demonstrate proper lifting techniques and hazard awareness # LI-Onsite 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!

Responsibilities

The Manufacturing Technician will support the manufacturing of nasal spray medications by operating and monitoring production equipment, cleaning and maintaining manufacturing areas, and completing production documentation. Collaboration with cross-functional teams will be essential to improve patient outcomes globally.