Role at a glance
- Job function
-
Manufacturing & Skilled Trades Quality Assurance & Quality Control
- Salary
- Not Disclosed
- Location
- Cincinnati, Ohio, United States
- Work arrangement
- On-site
- Employment
- Full-time
- Education
- Bachelor's degree or equivalent in Chemistry, Biology, Biochemistry, or a related scientific field.
- Visa support
- Must be Legally authorized to work in the United States without sponsorship.
Spotted an issue?
We’ll check it against the original posting.
Role Summary
This QC Scientist I role at the Cincinnati Oral Solid Dose site supports pharmaceutical manufacturing by testing raw materials, in-process samples, finished products, and stability samples. The role uses established analytical methods and laboratory instruments while following applicable quality, documentation, and safety requirements.
What You'll Do
- Perform chemical, physical, and, as assigned, microbiological testing using established procedures.
- Use analytical techniques such as HPLC, GC, spectroscopy, dissolution testing, and wet chemistry methods, as applicable.
- Support microbiological testing, environmental monitoring, and aseptic practices, as assigned.
- Prepare test solutions and maintain laboratory instruments and work areas.
- Document work and results accurately in laboratory records and applicable systems.
- Identify and communicate unexpected results or testing issues in accordance with procedures.
Generated from the employer's posting. Verify important details before applying.
View full postingQualifications
Bachelor's degree or equivalent in chemistry, biology, or a related scientific field, with analytical testing familiarity, GMP knowledge, and cleanroom work requirements.
Required
- Bachelor's degree or equivalent in Chemistry, Biology, Biochemistry, or a related scientific field
- Equivalent combinations of education, training, and relevant work experience may be considered
- Legally authorized to work in the United States without sponsorship
- Must be able to pass a comprehensive background check to include drug screening
- Familiarity with analytical methods such as HPLC, GC, spectroscopy, dissolution testing, and wet chemistry
- Knowledge of GMP, laboratory documentation, and pharmaceutical quality practices
- Strong attention to detail, problem-solving, and written and verbal communication skills
- Proficiency with Microsoft Office and laboratory information systems
Preferred
- One year of relevant experience
- Experience in a pharmaceutical or other regulated environment
- Experience with microbiological testing, environmental monitoring, or aseptic techniques
Original job description
Content provided by the employer
Original job description
Content provided by the employer
Work Schedule
Standard (Mon-Fri)Environmental Conditions
Able to lift 40 lbs. without assistance, Adherence to all Good Manufacturing Practices (GMP) Safety Standards, Cleanroom: no hair products, jewelry, makeup, nail polish, perfume, exposed piercings, facial hair etc... allowed, Laboratory Setting, Some degree of PPE (Personal Protective Equipment) required (safety glasses, gowning, gloves, lab coat, ear plugs etc.), Strong Odors (chemical, lubricants, biological products etc.), Will work with hazardous/toxic materialsJob Description
Site Overview
With the support of more than 800 employees, Thermo Fisher Scientific’s Oral Solid Dose (OSD) site in Cincinnati provides drug development and commercial manufacturing services. The site specializes in advanced dosage forms, including controlled- and sustained-release products, osmotic release dosage forms using laser drilling, liquid-filled hard capsules, controlled substances, and abuse-deterrent technologies.
About Thermo Fisher Scientific
At Thermo Fisher Scientific, you’ll contribute to work that helps customers make the world healthier, cleaner, and safer. The company supports colleagues’ career growth and uses science to address important challenges around the world.
Role Summary
As a QC Scientist I, you will support pharmaceutical manufacturing by testing raw materials, in-process samples, finished products, and stability samples. You will use established analytical methods and laboratory instruments to help ensure product quality while following applicable quality, documentation, and safety requirements.
What You’ll Do
- Perform chemical, physical, and, as assigned, microbiological testing using established procedures.
- Test raw materials, in-process samples, finished products, and stability samples.
- Use analytical techniques such as HPLC, GC, spectroscopy, dissolution testing, and wet chemistry methods, as applicable.
- Support microbiological testing, environmental monitoring, and aseptic practices, as assigned.
- Prepare test solutions and maintain laboratory instruments and work areas.
- Document work and results accurately in laboratory records and applicable systems.
- Identify and communicate unexpected results or testing issues in accordance with procedures.
- Follow applicable GMP, SOP, data integrity, and safety requirements.
How will you get here?
*Must be Legally authorized to work in the United States without sponsorship.
*Must be able to pass a comprehensive background check to include drug screening.
*Relocation assistance is not provided.
Education
- Bachelor’s degree or equivalent in Chemistry, Biology, Biochemistry, or a related scientific field.
- Equivalent combinations of education, training, and relevant work experience may be considered.
Experience
- One year of relevant experience is preferred but not required.
- Experience in a pharmaceutical or other regulated environment is preferred.
Knowledge, Skills, Abilities
- Familiarity with analytical methods such as HPLC, GC, spectroscopy, dissolution testing, and wet chemistry.
- Experience with microbiological testing, environmental monitoring, or aseptic techniques is an advantage.
- Knowledge of GMP, laboratory documentation, and pharmaceutical quality practices.
- Strong attention to detail, problem-solving, and written and verbal communication skills.
- Proficiency with Microsoft Office and laboratory information systems.
- Ability to work independently and collaboratively.
Work Environment and Physical Requirements
- Ability to stand and walk for extended periods, perform laboratory tasks requiring manual dexterity, and lift up to 50 pounds.
- Ability to work in cleanroom environments while wearing required personal protective equipment (PPE).
- Flexibility to work shifts, including nights, weekends, or holidays, as needed.
The above statements are intended to describe the general nature and level of the work being performed by people assigned to this job. They are not a comprehensive list of all the duties and responsibilities associated with it.
Competitive wages & Excellent benefits package
- Review our company’s Total Rewards
- Medical, Dental, & Vision benefits-effective Day 1
- Paid Time Off & Holidays
- 401K Company Match up to 6%(after 1 year)
- Tuition Reimbursement – eligible after 90 days
- Employee Referral Bonus
- Employee Discount Program
- Recognition Program
- Charitable Gift Matching
- Company Paid Parental Leave
- We will provide the vital equipment for your role including: computer, monitor, keyboard, mouse, etc.
- We also provide any Personal Protective Equipment you may need including: lab coats, safety glasses, safety shoes, etc.
For more information on our benefits, please visit: https://jobs.thermofisher.com/global/en/total-rewards
About the company
Thermo Fisher Scientific
Large Enterprise
Thermo Fisher Scientific is a global leader in serving science, providing a wide range of analytical instruments, reagents, and software solutions for healthcare, pharmaceuticals, and life sciences research. With a commitment to innovation and quality, the company enables customers to make significant advancements in scientific discovery and healthcare diagnostics. Thermo Fisher operates in more than 50 countries and employs over 80,000 people, fostering a collaborative environment aimed at enhancing global health and safety. Through its broad portfolio of brands and technologies, the company plays a vital role in accelerating life-changing research and improving patient outcomes worldwide.