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
The
Converting Technician is responsible for supporting the safe and efficient operation of TDD production lines while ensuring compliance with established quality, safety, and GMP requirements. This role performs routine manufacturing activities including equipment operation, material handling, line clearances, production documentation, inspections, and basic changeover support under the guidance of Setup Technicians, Leads, Supervisors, and other qualified personnel.
The Converting Technician is expected to develop a strong understanding of manufacturing processes, equipment operation, and regulatory requirements while contributing to production goals, product quality, and operational efficiency. The role requires attention to detail, adherence to standard operating procedures, and a commitment to safety, teamwork, and continuous learning.
Essential Duties & Role Responsibilities
- Operate TDD manufacturing equipment in accordance with approved work instructions, SOPs, batch records, and production schedules.
- Monitor equipment and processes to ensure products are manufactured safely, efficiently, and in compliance with quality standards.
- Perform routine operational tasks including material loading, product monitoring, packaging, and equipment housekeeping.
- Escalate equipment, process, quality, or safety concerns to appropriate personnel when identified.
- Assist with line setups, product changeovers, and startup activities.
- Prepare equipment, tooling, materials, and components required for production runs.
- Support line clearance activities before and after production campaigns.
- Verify equipment and materials are staged and ready to support scheduled production activities.
- Adhere to all Good Manufacturing Practices (GMP), Good Documentation Practices (GDP), SOPs, and company policies.
- Perform in-process inspections and quality checks as required by procedures and production documentation.
- Identify and report nonconformances, discrepancies, or product quality concerns.
- Support investigations and corrective actions by providing accurate and timely information.
- Accurately complete production records, logbooks, batch documentation, and electronic systems in compliance with GDP requirements.
- Document production activities, downtime events, material usage, and process observations as required.
- Ensure all documentation is complete, legible, accurate, and attributable.
- Maintain production records in accordance with regulatory and company requirements.
- Move, stage, and manage raw materials, packaging components, and finished goods in accordance with established procedures.
- Verify material identification, status, and usage prior to production activities.
- Perform inventory transactions and material reconciliation activities as required.
- Operate material handling equipment following training and qualification requirements.
- Follow all environmental, health, and safety policies and procedures.
- Utilize required personal protective equipment (PPE) and maintain safe work practices at all times.
- Report unsafe conditions, near misses, and incidents promptly.
- Participate in safety initiatives, inspections, and continuous improvement activities.
- Work collaboratively with Production Operators, Maintenance, Quality, and Production leadership to achieve departmental objectives.
- Participate in training programs and continuously develop manufacturing and technical skills.
- Contribute ideas and recommendations that improve safety, quality, productivity, and operational efficiency.
- Support departmental initiatives focused on Lean Manufacturing and continuous improvement.
- Successfully complete all required training and qualification programs.
- Maintain competency on assigned equipment and manufacturing processes.
- Demonstrate a willingness to learn new equipment, procedures, and responsibilities.
- Progressively develop the technical knowledge and skills necessary to support advancement opportunities within the TDD organization.
Required Skills And Experience
- High School Diploma or GED required.
- Previous manufacturing experience preferred; experience in a regulated environment such as pharmaceutical, medical device, food, or consumer products manufacturing is a plus.
- Ability to learn and operate TDD manufacturing equipment in accordance with established procedures, work instructions, and SOPs.
- Basic understanding of Good Manufacturing Practices (GMP), Good Documentation Practices (GDP), safety requirements, and quality standards, or the ability to learn and apply them effectively.
- Strong attention to detail and ability to accurately complete production documentation and records.
- Ability to follow verbal and written instructions while maintaining compliance with production, quality, and safety requirements.
- Basic computer skills and ability to utilize manufacturing systems, electronic documentation systems, and training platforms.
- Effective verbal and written communication skills and the ability to work collaboratively within a team environment.
- Demonstrated reliability, accountability, and a positive attitude toward learning and continuous improvement.
- Ability to support setup, changeover, line clearance, material handling, and production activities under the direction of qualified personnel.
- Forklift certification or experience preferred; ability to safely operate powered industrial trucks after successful training and qualification.
- Ability to work any shift, including 1st, 2nd, 3rd shift, weekends, holidays, and overtime as required to support business needs.
- Physically capable of lifting up to 50 pounds and performing repetitive manufacturing tasks.
- Ability to stand, walk, bend, reach, climb stairs, and perform job duties for extended periods in a manufacturing environment.
- Demonstrated commitment to safety, product quality, teamwork, and compliance.
California residents should review our
Notice for California Employees and Applicants before applying.
The expected compensation range for this position represents a good faith estimate. The specific compensation offered to a candidate may vary based on factors including, but not limited to, the candidate’s relevant knowledge, training, skills, work location, and/or experience. In addition, this position may be eligible for a range of benefits (e.g., Medical, Dental, & Vision, Health Savings Accounts, Flexible Spending Accounts, Disability Benefits, Life Insurance, Voluntary Benefits, Paid Absences, and 401k Benefits, etc.).
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.
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