QC Analytical Scientist (Sun-Wed)

Eurofins PSS Insourcing Solutions; Sanford (NC); On-site; USD 42,000 - 66,000; Full time

Benefits offered by this job

Medical insurance

Dental insurance

Vision insurance

Life insurance

Disability insurance

401(k) with company match

Paid vacation and holidays

Job summary

Eurofins USA PSS Insourcing Solutions seeks a full-time Analyst to perform routine and non-routine analytical testing of pharmaceutical products and raw materials in a GMP-regulated laboratory in Sanford, NC. You will operate instruments such as HPLC, UPLC, UV-VIS, pH meters, TOC and other equipment, ensuring accuracy and proper documentation.

The role requires a BS in Chemistry or Biochemistry and hands-on lab experience; preferred familiarity with Empower 3 or LIMS and ability to work across

Qualifications

• Experience in a GMP/CGMP environment is preferred.
• Experience with analytical standards, reagents and laboratory instruments.
• Strong analytical and data analysis skills; accurate pipetting; multi-tasking capability.

Responsibilities

• Perform routine and non-routine analytical testing of pharmaceutical products and materials.
• Operate and maintain analytical instrumentation and document results per GMP.
• Collaborate with Quality Operations and other teams to support investigations and investigations actions.
• Maintain laboratory compliance and ensure reliable, high-quality results for site operations.

Education

BS in Chemistry or Biochemistry

Tools

LIMS

Empower 3

Job 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 role performs routine and non-routine analytical testing of pharmaceutical products, raw materials, validation, stability, and process samples within a GMP-regulated laboratory.

• Independently manage testing priorities, operate and maintain analytical instrumentation, evaluate data for accuracy and compliance, and ensure complete and accurate documentation
• Collaborate closely with Quality Operations and may interact with manufacturing, engineering, environmental health and safety, technical services, research teams, and external laboratories as needed
• Responsibilities also include supporting investigations, corrective actions, inventory management, material ordering, and maintaining laboratory compliance while delivering reliable, high-quality analytical results that support site operations
• Utilize laboratory instruments and equipment in accordance with established procedures to include but not limited to appearance hoods, pH meters, conductivity meters, Solo VPE, Osmometers, UV-VIS, HPLC, UPLC, TOC and conductivity, and various other instruments
• Responsible for appropriate creation, review and approval of GMP documentation (test records, and as assigned validation protocols/reports, test methods, equipment records, etc.)

The site is not accessible by public transportation options.

Qualifications

Minimum Qualifications:

• BS in Chemistry or Biochemistry with a minimum of 2 years of experience working in a laboratory environment, QC laboratory preferred.
• Experience working with analytical standards, reagents, and laboratory instruments
• Successful hands-on analytical testing experience in a Good Manufacturing Practices {also cGMP} environment
• Understanding and performing analytical testing and the use of analytical equipment: i.e. UV-VIS, HPLC, UPLC, pH, appearance, osmolality, TOC and conductivity
• Capability to perform complex mathematical problems and perform complex data analysis
• Accurate pipetting skills
• Strong organizational skills and ability to multi-task across projects and activities
• Must be self-motivated and work with minimal direction
• Must be authorized to work in the United States indefinitely without restrictions or sponsorship

Preferred Experience

• Empower 3, LIMS
• Demonstrate proficiency in computerized systems, such as Laboratory Information Management System

Additional Information

This position is Full-Time, Sunday to Wednesday 7 am - 5 pm. 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.