Formulation Technician - 3rd Shift

Guerbet; Raleigh (NC); On-site; USD 42,000 - 62,000; Full time

Job summary

Guerbet, a global leader in medical imaging, seeks a Formulation Technician to operate in a cGMP production environment, preparing pharmaceutical formulations and supporting filling teams. You will verify batch records, manage materials in SAP, perform aseptic transfers, document processes, and ensure sanitation and regulatory compliance.

This role requires a High School diploma or GED, 1–3 years of pharma manufacturing experience, and strong aseptic technique; teamwork, attention to detail, and

Qualifications

• High School diploma or GED completed.
• 1–3 years in pharmaceutical manufacturing preferred.
• Compounding or formulation experience preferred.
• Strong aseptic processing and cleanroom knowledge.
• Basic computer skills and familiarity with SAP.

Responsibilities

• Demonstrate understanding of cGMP and regulatory guidelines in a clean room.
• Prepare media according to batch records and SOPs; verify identities.
• Perform controlled transfers of API into formulation vessels.
• Prepare and review process documentation for accuracy and compliance.
• Ensure sanitation and aseptic technique; maintain safety and productivity.
• Assist in investigations of contamination or deviations.

Skills

Aseptic processing

Media preparation

Documentation

SAP inventory

GMP compliance

Education

High School diploma or GED

Tools

SAP

Microsoft Office

Job description

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 alsobe responsible forcompleting allnecessarydocumentationrelatedto the manufacturing processwhileadheringto cGMP andGDPguidelines.

YOUR ROLE

• 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.
• Ensurea highlevel of safety, quality, and productivity tomaintaina reliable supply of products to patients.
• Promptly report andassistin investigationof any contamination events or deviations.
• Performs other duties as assigned by management

Department Specific/Non-Essential Functions

• Collaborate with Engineering, Validation, and otherdepartmentsininitiating and implementingprograms such asContinuousImprovement (Leanand 5S) andTotal Productive Maintenance.
• Prevent excess wasteofproduct 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

Required Qualifications

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

Cognitive Requirements

• Strongverbal and interpersonal communication skills.
• Excellent reading comprehension and attention to detail for interpreting batch records and SOPs.
• Strong mathematical aptitude foraccuratemeasurements and calculations.
• Ability to read and understand military time isrequired
• Mental and visual acuity for production of quality product.
• Highly skilled in problem-solving anddiagnosticabilities.
• Ability to work effectively as part of a team to meet production goals
• Demonstrates initiative and sound decision making while working effectively both independently and as part of a team.

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.