Production Technician (Days)

U469 (FCRS = US469) AAA USA Inc.; Indianapolis (IN); Sur place; USD 35 000 - 64 000; Plein temps

Avantages offerts par ce poste

Health benefits

401(k) match

Paid time off

Résumé du poste

Novartis in Indianapolis seeks a Production Technician to support isotope product manufacturing. You will operate isolators, follow batch records, and uphold ALARA radiation safety while ensuring quality and regulatory compliance.

Role requires a scientific degree and GMP experience; on-site work with a focus on safety, training, and documentation. Competitive benefits apply in the US.

Qualifications

• High school diploma or equivalent required; Bachelor's degree preferred.
• Minimum 2 years in GMP or aseptic manufacturing environment.
• Knowledge of GMP regulations and regulated manufacturing environments.

Responsabilités

• Execute manufacturing activities for isotope products per batch records and procedures.
• Operate and maintain Grade C isolators for safe production operations.
• Follow radiation safety requirements including ALARA principles.
• Perform contamination control and monitoring per site procedures.
• Support equipment cleaning, sterilization, and readiness of manufacturing areas.
• Complete production documentation including batch records and training records.
• Participate in qualification and validation activities to ensure compliance.

Connaissances

Forklift Operations

GMP Compliance

Inventory Management

Machine Operations

Production Management

Quality Control

Regulatory Documents

Formation

Bachelor's degree in a scientific discipline

Outils

None

Description du poste

Band Level 2 Job Description Summary As a Production Technician, you will play an active role in the daily production of isotopes used in advanced radioligand therapies while supporting the setup, preparation, and operation of equipment and manufacturing systems. Working as a qualified radiation worker in a controlled manufacturing environment, you will execute production activities in accordance with batch records, standard operating procedures, and regulatory requirements. Partnering closely with Production Leads and Managers, you will help ensure manufacturing operations are performed safely, efficiently, and on schedule while contributing to therapies that help transform outcomes for patients. Job Description #LI-Onsite Shift: Monday - Friday Days (A Shift) Location: Indianapolis, IN, United States Relocation Support: This role is based in Indianapolis, IN, United States. Novartis is unable to offer relocation support: please only apply if accessible.

Key Responsibilities

• Execute manufacturing activities for isotope products in accordance with batch records and established procedures.
• Operate and maintain Grade C isolators while supporting safe, compliant production operations.
• Follow radiation safety requirements, including dosimetry, personal protective equipment, and ALARA principles.
• Perform contamination control, personnel monitoring, and material monitoring in accordance with site procedures.
• Support production readiness through equipment cleaning, sterilization, and preparation of manufacturing areas.
• Conduct routine and dynamic environmental monitoring to maintain manufacturing readiness and compliance.
• Prepare, verify, and maintain materials in accordance with defined batch monitoring procedures.
• Participate in qualification and validation activities to support operational readiness and process compliance.
• Complete production documentation, including batch records, shipping documents, and training records.
• Support a culture of safety, quality, current Good Manufacturing Practice compliance, and open communication within the manufacturing team.

Essential Requirements

• High school diploma or equivalent required;
• Bachelor's degree in a scientific discipline strongly preferred.
• Minimum 2 years of experience in a current Good Manufacturing Practice or aseptic manufacturing environment.
• Minimum 2 years of pharmaceutical manufacturing experience; low-bioburden manufacturing experience preferred.
• Knowledge of current Good Manufacturing Practice regulations and regulated manufacturing environments.
• Ability to work safely with radioactive materials in a controlled manufacturing environment.
• Experience following standard operating procedures, batch records, and manufacturing documentation.
• Ability to wear cleanroom garments, personal protective equipment, and required respiratory protection.
• Strong attention to detail, communication skills, and commitment to safety, quality, and compliance.

Desirable Requirements

• Training in radiochemistry or radiopharmacy strongly preferred.
• Hands‑on experience in radiochemistry, isotope production, or radiopharmaceutical manufacturing with radioactive materials in a Good Manufacturing Practice environment strongly preferred.

Salary

• The salary for this position is expected to range between $25.19 and $46.82 per hour.
• Salary Range $52,400.00 - $97,400.00

Benefits

• US‑based eligible employees will receive a comprehensive benefits package that includes health, life and disability benefits, a 401(k) with company contribution and match, and a variety of other benefits.
• In addition, employees are eligible for a generous time off package including vacation, personal days, holidays and other leaves.
• Your compensation will include a performance‑based cash incentive and, depending on the level of the role, eligibility to be considered for annual equity awards.

Skills Desired

• Forklift Operations
• GMP Compliance
• Health, Safety, and Environment (HSE) Policy
• Inventory Management
• Machine Operations
• Manufacturing
• Operations Management
• Process Improvements
• Production Management
• Quality Control (QC)
• Regulatory Documents

Improving the lives of people living with disease takes more than innovative science. It takes a focus on the needs of people and a community committed to meeting them. It takes a team of people like you. Working together. Learning together. Thriving together. Discover how you can join us in changing people's lives.

To learn more about the culture, rewards and benefits we offer our people.

EEO Statement

The Novartis Group of Companies are Equal Opportunity Employers. We do not discriminate in recruitment, hiring, training, promotion or other employment practices for reasons of race, color, religion, gender, national origin, age, sexual orientation, gender identity or expression, marital or veteran status, disability, or any other legally protected status. We strive to create an inclusive workplace that cultivates bold innovation through collaboration and empowers our people to unleash their full potential.

Accessibility and reasonable accommodations

The Novartis Group of Companies are committed to working with and providing reasonable accommodation to individuals with disabilities. If, because of a medical condition or disability, you need a reasonable accommodation for any part of the application process, or in order to perform the essential functions of a position, please send an e-mail to [e-mail] call [phone] and let us know the nature of your request and your contact information. Please include the job requisition number in your message.