QC Scientist II stabilityrelease (1st shift)
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Job Location:
Greenville - USA
Monthly Salary:
Not Disclosed
Posted on:
30+ days ago
Vacancies:
1 Vacancy
Job Summary
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 an 8-Hour Day schedule. Hours will typically 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 addition recommend solutions to problems that arise ensure quality of product work with downstream departments and maintain a safe work environment.
Keys to Success:
Education
Bachelor Degree in Chemistry Biochemistry Molecular Biology or related physical/biological science field highly preferred. An associates degree is minimally required.
Experience
At least 3 years of related experience performing tests or analyses for pharmaceutical in-process samples or finished product samples with the possession of a Bachelors degree. More years of experience will be required with the possession of an associates degree.
1 years of chromatographic data acquisition systems and HPLC experience preferred.
Knowledge Skills Abilities
Knowledge of Trackwise supporting product investigations and deviations.
Good 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 customers
Benefits
We offer competitive remuneration annual incentive plan bonus healthcare and a range of employee benefits including:
Benefits & Total Rewards Thermo Fisher Scientific
Medical Dental & Vision benefits-effective Day 1!
Paid Time Off & Designated Paid Holidays
Retirement Savings Plan (401K)
Stock Options
Tuition Reimbursement
Employee Referral Bonus
Career Advancement Opportunities
Annual 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!
Key Skills
- Laboratory Experience
- Immunoassays
- Machine Learning
- Biochemistry
- Assays
- Research Experience
- Spectroscopy
- Research & Development
- cGMP
- Cell Culture
- Molecular Biology
- Data Analysis Skills
About Company
Electron microscopes reveal hidden wonders that are smaller than the human eye can see. They fire electrons and create images, magnifying micrometer and nanometer structures by up to ten million times, providing a spectacular level of detail, even allowing researchers to view single a ... View more
