Thermofisher
Direct Workday career site

Scientist II - Analytical R&D

Location
Florence, SC
Listed
5 days ago

About the role

  • 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.)

About the role

How will you make an impact?

The Scientist II conducts laboratory work as necessary to assure that products are tested per operating procedures. Ensure that work is carried out in an efficient and safe manner. Uses judgment in making adaptation and modifications on all assignments. Provides routine and non-routine analyses in an analytical chemistry laboratory following standard practices.

Performs analytical methods as assigned for testing on raw materials, samples, stability, production intermediates, and active pharmaceutical ingredients, including method development and qualification activities. Supports internal development and/or manufacturing operations. Makes detailed observations and reviews, documents, and communicates test results internally and externally to clients.

Location: Florence, SC

Hours: Mon-Fri 8am-5pm (must be flexible)

Key Responsibilities

  • Consistently aligns with housekeeping standards.
  • Maintains a clean and safe work environment including work area, instrumentation, and testing materials.
  • Understands and works in compliance with all cGMP, OSHA, and safety regulations, BOPs and SOPs.
  • Performs cGMP procedures, lab procedures, BOPs and SOPs.
  • Performs daily instrument calibrations / verifications as required.
  • Responsible for weekly/monthly inspection of safety equipment.
  • Assembles and operates laboratory (bench scale) equipment and carries out experiments independently.
  • Conducts routine and non-routine chemical testing and method development/qualification for pharmaceutical raw materials, in-process samples, and active pharmaceutical ingredient samples by internally developed and compendial test methods.
  • Performs developmental and validated test methods using HPLC, GC, spectroscopy, GC/MS, LC/MS, and/or traditional wet chemical testing, and trains other employees on these techniques.
  • Provides thoughtful technical review of data collected by other employees.
  • Recognizes and reports/investigates out-of-specification or unexpected results and non-routine analytical and product problems.
  • Clearly and accurately communicates the results of work by documenting the testing/analysis and obtained results. Records and reports results of analysis in accordance with prescribed lab procedures and systems.
  • Assists in preparing regulatory documents and other communications with outside agencies, clients, and/or colleagues from other corporate sites.
  • Writes and reviews Analytical Methods, validation protocols, validation reports, and SOPs if needed.
  • Solves problems related to the processing of chemical procedures.
  • Ability to drive functional, technical and operational excellence. Ability to inspire and drive team effectiveness. Good knowledge of medical terminology, clinical data, and Good Manufacturing Practices (GMP). Strong proficiency in Microsoft Office Suite (Word, Excel, and PowerPoint. Effective written, interpersonal, and presentation skills. Ability to work on multiple projects simultaneously.
  • Position requires ordinary ambulatory skills and physical coordination sufficient to move about office locations; ability to stand, walk, stoop, kneel, crouch periodically for prolonged periods of time; manipulation (lift, carry, move) of light to medium weights of 10-35 pound pounds; arm, hand and finger dexterity, including ability to grasp and type for prolonged periods of time; visual acuity to use a keyboard, computer monitor, operate equipment, and read materials for prolonged periods of time; ability to sit, reach with hands and arms, talk, and hear for prolonged periods of time.

How will you get here?

*Must be able to pass a comprehensive background check to include drug screening.

Education

  • Bachelor's degree in chemistry or related field required.

Experience

  • 2+ years of experience working in a laboratory preferred, (GLP or GMP/cGMP environment preferred)
  • 2+ years of experience working with analytical instrumentation, such as HPLC, GC, CE, ICP and dissolution apparatus preferred

*Equivalent combinations of education, training, and relevant work experience may be considered.

Knowledge, Skills, Abilities

  • Extensive knowledge and understanding of chemistry and analytical instrumental technologies.
  • Extensive knowledge of qualitative and quantitative chemical analysis.
  • Extensive knowledge of quality and regulatory requirements in the pharmaceutical industry, including pharmaceutical GMPs and descriptive organic chemistry.
  • Good problem-solving skills and logical approach to solving scientific problems.
  • Proficiency with HPLC, GC, LC/MS and Dissolution techniques.
  • Good interpersonal and communication skills (both oral and written).
  • Good presentation skills to present information to customers, clients, and other employees.
  • Ability to read, analyze, and interpret technical procedures and governmental regulations.
  • Ability to write standard operating procedures, simple protocols, and reports.

Ability to respond to common inquiries or complaints from customers or regulatory agencies. Ability to apply mathematical operations, to such tasks as determination of test reliability, analysis of variance and correlation techniques.

Physical Requirements

Position requires ordinary ambulatory skills and physical coordination sufficient to move about office locations; ability to stand, walk, stoop, kneel, crouch periodically for prolonged periods of time; manipulation (lift, carry, move) of light to medium weights of 10-35 pound pounds; arm, hand and finger dexterity, including ability to grasp and type for prolonged periods of time; visual acuity to use a keyboard, computer monitor, operate equipment, and read materials for prolonged periods of time; ability to sit, reach with hands and arms, talk, and hear for prolonged periods of time.

  • Safety glasses, safety shoes, lab coat, latex or similar gloves, safety apron, organic respirator occasionally.
  • 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.
Read the original posting

From Thermofisher's careers page, first listed on Rolev.ai on November 5, 2026. Rolev.ai is not the employer.

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Common questions

Where is the Scientist II - Analytical R&D job at Thermofisher located?

This Scientist II - Analytical R&D position at Thermofisher is located in Florence, SC. Always check Thermofisher's application page for specific state eligibility or relocation policies.

How do I apply for the Scientist II - Analytical R&D position at Thermofisher?

This listing links directly to Thermofisher's Workday application page. You can apply directly on Thermofisher's site, or use Rolev.ai to check your resume fit, generate a zero-hallucination tailored resume and cover letter for this posting, and autofill the Workday application form in 1 click with the Rolev.ai Chrome extension. You always review the form and press Submit yourself.