GMP Production Associate

- Regular/Permanent

- USA / Texas

- In Office

Welcome to Orano

Helping to meet current and future challenges to preserve our world and build the world of tomorrow while taking care of everyone's health is stimulating for you. For us too. By joining the Orano Group, a leading international player in the nuclear industry, you are in the right place.

Every day we work to produce efficient low-carbon energy, to fight global warming, to find solutions that save natural resources, and to contribute to progress in health.

Our strengths? Across the entire fuel cycle, we have extensive expertise in cutting-edge technologies, safe, high value-added products and services, and a strong capacity for innovation. All of these factors reflect the strong skills of our 17,000 employees, whom we are constantly striving to develop. With their different backgrounds and experience, they are proof of our openness to all talents. They share the same ambition: to give nuclear energy its full value.

Job description

Orano Med Theranostics

Orano Med is seeking a detail-oriented GMP Production Associate

This position is primarily responsible for manufacturing GMP clinical materials and products. This position is also responsible for maintaining the GMP production suite and GMP equipment, as well as ensuring that all necessary documentation is maintained accurately in accordance with all applicable regulations. The GMP Production Associate performs clinical product manufacturing as well as preparation for clinical product manufacturing. This position conducts cleaning and routine maintenance of areas and equipment, edits documents, and maintains accurate records of operations within GMP suite.

Key Responsibilities

All Production Associate levels:

- Follow written procedures for clinical and non-clinical manufacturing as primary operator or verifier

- Participate in release testing of cold vials and solutions

- Complete batch records, forms, equipment logs, and other production records as directed per company procedures and GMP guidelines

- Work concurrently with Quality Assurance (QA),Quality Control (QC), and Logistics personnel to deliver a high-quality product

- Adhere to production schedules and timelines

- Execute room and equipment preparation for manufacturing operations

- Perform room sanitization activities to maintain controlled environment conditions

- Participate in isolator and room monitoring

- Maintain stock of manufacturing raw materials and obtain necessary documentation to submit for release

- Identify and communicate common equipment/process failures and report to supervisor

- Participate in deviation investigations

- Clean, sanitize and sterilize equipment and components to support production operations

- Initiate cleaning procedures for the labs, perform daily checks and routine maintenance on equipment, restock labs.

- Maintain up-to-date training on all manufacturing records

- Assist in review of manufacturing documents

- Maintain gowning and production qualifications

Orano strives to provide a total compensation package that brings value to our employees. We also offer highly competitive health and wellness programs, 401(k) contributions, and industry leading paid time off.

Our Full-Time Benefits

- Competitive compensation

- Health, Dental, and Vision insurance – with generous employer contributions

- 401(k) with employer matching and contribution amounts

- Life insurance and Short- and Long-Term Disability insurance provided by the company

- Generous Paid Time Off and holiday schedules

- Numerous Training and Development opportunities

- and more…

Ideal qualifications

Education & Experience

All candidates must meet the following minimum requirements in order to be considered for this opportunity. Candidates who exceed minimum qualifications may be considered for a higher-level position.

Minimum Qualifications:

- Bachelors degree in a related field or comparable work experience

- 1+ year's experience

Required Skills & Competencies:

- Demonstrated skills in GMP manufacturing and documentation requirements.

- Proficient in aseptic technique.

- Ability to work side by side with the quality assurance department.

- Ability to maintain inventory of raw materials.

- Ability to troubleshoot equipment and process failures

- Excellent documentation skills and attention to detail

- Excellent communication, problem-solving and organizational skills

- Ability to follow written and verbal instruction and work under supervision or independently

- Computer literacy and proficiency with Microsoft Office

- Ability to understand and exercise basic mathematical calculations and more complex calculations with various available tools and calculators

- Ability to work in a very fast-paced, high-growth team environment

- Ability to stand, crouch, sit, bend, or stretch for extended periods of time

- Demonstrate ability to perform duties using proper aseptic technique and following ALARA principles for working with radioactive materials

Preferred Skills & Competencies:

- Demonstrate ability to perform tasks with minimal guidance once trained

- Teamwork

Orano is an Equal Opportunity/Affirmative Action employer. All qualified applicants will receive consideration for employment without regard to race, color, religion, gender, national origin, age, disability, citizenship, veteran status, marital status, sexual orientation, gender identity, genetic predisposition or carrier status or any other characteristic protected by law.