QC Method Transfer and Validation Scientist

Eurofins; Sanford (NC); On-site; USD 85,000 - 120,000; Full time

Benefits offered by this job

Medical coverage

Dental coverage

Vision coverage

Life insurance

Disability insurance

401(k) with company match

Paid vacation and holidays

Job summary

Eurofins Scientific in Sanford, NC, seeks a QC Method Transfer and Validation Scientist to lead method qualification, transfer, and validation activities for biologic testing in a GMP-compliant environment. The role requires strong technical expertise and collaboration with internal and external partners.

You will perform data analysis, generate protocols and reports, and troubleshoot analytical techniques such as HPLC, CE, and ELISA. On-site with some flexibility for outside hours and weekends.

Qualifications

• BS in Chemistry or similar field with a minimum of 4 years of laboratory experience.
• Experience with proteins or carbohydrates.
• Experience in a GMP/cGMP environment.
• Experience with analytical standards, reagents, and laboratory instruments.
• HPLC experience and Empower 3.
• Familiarity with USP and EU guidelines.
• Strong communication and problem-solving skills.
• Flexibility to support outside standard hours and potential weekend work.

Responsibilities

• Collaborate with internal and external partners to execute method qualification, validation protocols, and transfer documentation.
• Perform data analysis, protocol/report generation, and troubleshoot analytical techniques (HPLC, CE, ELISA).

Skills

HPLC

Empower 3

Problem solving

Communication skills

Independent work

Education

BS in Chemistry or similar field

Tools

Empower 3

Job description

QC Method Transfer and Validation Scientist

Full-time

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.

This position is responsible for supporting analytical method transfer and validation activities to ensure robust and compliant testing of biologic products. The role requires strong technical expertise and attention to regulatory requirements in a GMP-compliant environment.

• Collaborate with internal and external partners to execute method qualification, validation protocols, and transfer documentation.
• Perform data analysis, protocol/report generation, and troubleshooting analytical techniques such as HPLC, CE, and ELISA.

This role is on-site in Sanford, NC. Flexibilityto support outside standard hours and weekends is needed. The site is not accessible by public transportation options.

Required Qualifications:

• BS in Chemistry or similar field with a minimum of 4 years of experience working in a laboratory environment
• 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
• HPLC and Empower 3 Experience
• Familiarity with USP, EU guidelines
• Effective oral and written communication
• Strong problem-solving skills
• Flexible to support outside standard hours and potential for weekend support
• 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

Preferred Experience:

• Background with regulatory landscape

Position is full-time, Mon-Fri 8am-5pm. Flexibilityto support outside standard hours and weekends is needed.Candidates currently living within a commutable distance of Sanford, NC are encouraged to apply.

• Excellent full time benefits including comprehensive medical coverage, dental, and vision options
• Life and disability insurance
• 401(k) with company match
• Paid vacation and holidays

Eurofins USA PSS Insourcing Solutions is a Disabled and Veteran Equal Employment Opportunity employer.