Work Schedule

First Shift (Days)

Environmental Conditions

Adherence to all Good Manufacturing Practices (GMP) Safety Standards, Laboratory Setting, Some degree of PPE (Personal Protective Equipment) required (safety glasses, gowning, gloves, lab coat, ear plugs etc.)

Job Description

Location/Division Specific Information

This role is in the Quality Control Laboratory and will be performed at our Greenville, North Carolina location.

This is a 8-Hour Day schedule. Hours will be 8:00 AM to 5:00 PM Monday-Friday. Some night and weekend work may be required as needed to meet timelines.

Discover Impactful Work:

The Quality Control Scientist II will perform moderately complex analyses in a chemistry environment within defined procedures, practices, and analytical methods on in-process, finished drug product release, stability, and incoming bulk drug product samples. This position supports internal manufacturing operations, makes detailed observations, reviews documents, and communicates test results. In addition, recommend solutions to problems that arise, ensure quality of product, work with downstream departments, and maintain a safe work environment.

A day in the Life:Good knowledge of quality and regulatory requirements in the pharmaceutical industry, including pharmaceutical GMPs.Ability to read, analyze and interpret technical procedures.Good interpersonal and communication skills (both oral and written).Ability to write standard operating procedures, testing protocols and reports.Ability to respond to common inquiries or complaints from customers.Good knowledge and understanding of chemistry and analytical instrumental technologies.Good problem-solving skills and logical approach to solving scientific problems.Keys to Success:EducationBachelor Degree in Chemistry, Biochemistry, Molecular Biology, or related physical/biological science field minimally requireExperienceBachelor Degree in Chemistry, Biochemistry, Molecular Biology, or related physical/biological science field minimally required.3+ years related experience performing tests or analyses for pharmaceutical in-process samples or finished product samples. Knowledge of Trackwise supporting product investigations and deviations.1+ years of chromatographic data acquisition systems and HPLC experience preferred.Knowledge, Skills, AbilitiesGood knowledge and understanding of chemistry and analytical instrumental technologies.Good knowledge of quality and regulatory requirements in the pharmaceutical industry, including pharmaceutical GMPs.Ability to perform moderately complex analyses.Good problem-solving skills and logical approach to solving scientific problems.Good interpersonal and communication skills (both oral and written).Ability to read, analyze and interpret technical procedures.Ability to write standard operating procedures, testing protocols and reports.Ability to respond to common inquiries or complaints from customersBenefits

We offer competitive remuneration, annual incentive plan bonus, healthcare, and a range of employee benefits including:

Benefits & Total Rewards | Thermo Fisher ScientificMedical, Dental, & Vision benefits-effective Day 1!Paid Time Off & Designated Paid HolidaysRetirement Savings Plan (401K)Stock OptionsTuition ReimbursementEmployee Referral BonusCareer Advancement OpportunitiesAnnual Incentive Plan Bonus

Thermo Fisher Scientific offers employment with an innovative, forward-thinking organization, and outstanding career and development prospects. We offer an exciting company culture that stands for integrity, intensity, involvement, and innovation!