Job Description

Formulation Technician

At Guerbet, we build lasting relationships so that to enable people to live better This is Our Purpose.

We are a global leader in medical imaging, offering an extensive portfolio of pharmaceuticals, medical devices, digital and AI solutions, for diagnostic and interventional imaging. As a pioneer in the field of contrast products since the last 95 years ,we continuously innovate. We dedicate 10% of our revenue to Research & Development such as to improve the diagnosis, prognosis and quality of life of patients.

Achieve, Cooperate, Care and Innovate are the values ​​that we share and practice on a daily basis.

Working at Guerbet is not only being part of a multicultural team of 2,600 people across more than 20 countries, but, it is above all about playing a unique role in the future of medical imaging.

For more information on Guerbet, go to www.guerbet.com and follow Guerbet on Linkedin, Twitter, Instagram and Youtube

WHAT WE ARE LOOKING FOR

The Formulation Technician operates in full compliance with applicable hygiene, safety, quality, and regulatory standards, and in alignment with the organization’s framework, company’s procedures, and the defined scope of responsibility the role is accountable for.

The Formulation Technician is responsible for the processing and preparation of pharmaceutical formulations within a cGMP regulated production environment. The role also provides operational support to filling team members, ensuring a smooth transition of materials and consistent execution of upstream and filling processes. The Formulation Technician will also be responsible for completing all necessary documentation related to the manufacturing process while adhering to cGMP and GDP guidelines.

YOUR ROLE

Essential Functions:

• Demonstrate understanding of Current Good Manufacturing Practices (cGMP) and applicable regulatory guidelines (FDA, EMA, etc.) in a clean room environment requiring aseptic behavior.
• Prepare media according to approved batch records, SOPs, and cGMP requirements. Verify material identity, lot numbers, expiration dates, and required quantities through inventory systems, such as SAP
• Perform controlled transfers of API into designated formulation vessels or staging containers while adhering to segregation, containment, and safety procedures.
• Prepare and review process documentation to ensure accuracy, completeness, and compliance with cGMP and GDP requirements.
• Ensure compliance with all applicable regulatory agencies and cGMP requirements. Sanitize hold tanks, formulation tanks, process equipment, utensils, and conduct general cleaning of formulation processing areas according to cGMP and sanitation procedures.
• Maintain strict adherence to aseptic techniques during all operations within a controlled environment.
• Ensure a high level of safety, quality, and productivity to maintain a reliable supply of products to patients.
• Promptly report and assist in investigation of any contamination events or deviations. 
• Performs other duties as assigned by management

Department Specific/ Non-Essential Functions:

• Collaborate with Engineering, Validation, and other departments in initiating and implementing programs such as Continuous Improvement (Lean and 5S) and Total Productive Maintenance.
• Prevent excess waste of product and/or components by operating the equipment in an efficient manner.
• Report all safety and/or environmental incidents to management immediately.
• Cross-training to perform tasks and roles outside of the primary responsibilities
• Performs other duties as assigned by management

YOUR BACKGROUND

Education, Experience, and/or Skill:

• High School diploma, GED or equivalent.
• 1-3 experience in pharmaceutical manufacturing (preferred).
• Compounding or formulation experience (preferred)
• Strong knowledge of aseptic processing, cleanroom standards, and sterile techniques.
• Knowledge of basic computer skills and Microsoft Office.

Physical Requirements:

• Ability to stand for extended periods of time.
• Must be able to continuously lift a minimum of 50 Ibs.
• Ability to operate an electric pallet jack.
• Must be physically able to wear full aseptic gowning, including gloves, mask, and other protective gear, for extended periods while working in a controlled cleanroom environment.

Reason to join US

Much more than a Competitive salary,

We offer continued personal development. When you join Guerbet, you :

• Are choosing a global leader with recognized expertise in diagnostic and interventional imaging,
• Are joining our 2820 collaborators who are committed every day to offering innovative solutions to improve quality of patient’s life all over the world,
• Are joining a company where we value diversity of talents coming from various horizon.

We # Innovate # Cooperate # Care #Achieve at Guerbet.

Guerbet is an Equal Opportunity Employer. As an organization, we believe that no individual should be discriminated against because of their differences, which includes the following: age, disability, ethnicity, gender, gender identity and expression, religion, or sexual orientation. All employment decisions shall be made without regard to age, race, creed, color, religion, sex, national origin, ancestry, disability status, veteran status, sexual orientation, gender identity or expression, genetic information, marital status, citizenship status, or any other basis as protected by federal, state, or local law. Guerbet is committed to diversity, equity, and inclusion.

Guerbet provides accommodations to applicants and employees with disabilities. If you need an accommodation to apply for a position please send an email to careers@guerbet.com or you can also call this number +19843443717