QC Method Transfer and Validation Scientist (Sun-Wed)

Digitailor; Sanford (NC); On-site; USD 60,000 - 90,000; Full time

Job summary

Eurofins Scientific in Sanford, NC is seeking a laboratory professional to support analytical method transfer and validation of biologics.

You will work with GMP-compliant teams to perform method qualification, validation, and transfer documentation, plus data analysis and protocol/report generation using HPLC, CE, ELISA, and PCR.

Onsite role with occasional outside hours may apply; requires 2+ years in a lab and strong communication.

Qualifications

• BS in Chemistry or similar field with minimum 2 years of lab experience.
• Experience with proteins or carbohydrates.
• Experience in a GMP/cGMP environment.
• Strong communication skills, both oral and written.
• Proficient in analytical standards, reagents, and instruments.

Responsibilities

• Support analytical method transfer and validation for biologic products.
• Collaborate on method qualification, validation protocols, and transfer documentation.
• Data analysis, protocol/report generation, and troubleshooting using HPLC, CE, ELISA, PCR.
• Ensure compliance with GMP regulatory requirements.
• onsite in Sanford, NC; flexibility for outside standard hours.

Skills

Pipetting experience

Protein/Carbohydrate experience

GMP/cGMP experience

Oral and written communication

Problem-solving

Education

BS in Chemistry or similar field

Tools

HPLC

Empower 3

Job description

Company Description Eurofins Scientific is an international life sciences company, providing a unique range of analytical testing services to clients across multiple industries, to make life and our environment safer, healthier and more sustainable. From the food you eat, to the water you drink, to the medicines you rely on, Eurofins laboratories work with the biggest companies in the world to ensure the products they supply are safe, their ingredients are authentic and labelling is accurate. The Eurofins network of companies is the global leader in food, environment, pharmaceutical and cosmetic product testing and in agroscience Contract Research Organisation services. It is one of the market leaders in certain testing and laboratory services for genomics, discovery pharmacology, forensics, advanced material sciences and in the support of clinical studies, as well as having an emerging global presence in Contract Development and Manufacturing Organisations. It also has a rapidly developing presence in highly specialised and molecular clinical diagnostic testing and in-vitro diagnostic products. In over 30 years, Eurofins has grown from one laboratory in Nantes, France to 58,000 staff across a decentralised and entrepreneurial network of 900 laboratories in over 54 countries. Eurofins companies offer a portfolio of over 200,000 analytical methods to evaluate the safety, identity, composition, authenticity, origin, traceability and purity of biological substances and products. In 2021, Eurofins generated total revenues of EUR 6.72 billion, and has been among the best performing stocks in Europe over the past 20 years. Job Description This position is responsible for supporting analytical method transfer and validation activities to ensure robust and compliant testing of biologic products. Collaborate with internal and external partners to execute method qualification, validation protocols, and transfer documentation Data analysis, protocol/report generation, and troubleshooting analytical techniques such as HPLC, CE, and ELISA, PCR The role requires strong technical expertise and attention to regulatory requirements in a GMP-compliant environment This role is onsite in Sanford, NC. There are no public transportation options to the site. Ability to support outside standard hours may be needed.

Qualifications

• BS in Chemistry or similar field with a minimum of 2 years of experience working in a laboratory environment.
• Strong pipetting experience is required
• Experience working with proteins or carbohydrates.
• Experience working in a Good Manufacturing Practices {also cGMP} environment
• Experience working with analytical standards, reagents, and laboratory instruments
• Strong pipetting skills
• HPLC and Empower 3 experience
• Familiarity with USP, EU guidelines
• Effective oral and written communication
• Strong problem-solving skills
• Excellent oral and written communication skills as well as strong computer skills
• Must be organized, self-motivated, and capable of working independently or in a collaborative environment.
• Authorization to work in the United States indefinitely without restrictions or sponsorship

Additional Information This position is Full-Time, Sunday to Wednesday 7 am - 7 pm . Candidates currently living within a commutable distance of Sanford, NC are encouraged to apply. Excellent full-time benefits including compre