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Chemist

Job in Lexington, Fayette County, Kentucky, 40598, USA
Listing for: Piramal Pharma Limited
Full Time position
Listed on 2026-03-01
Job specializations:
  • Quality Assurance - QA/QC
    Data Analyst
  • Healthcare
Salary/Wage Range or Industry Benchmark: 60000 - 80000 USD Yearly USD 60000.00 80000.00 YEAR
Job Description & How to Apply Below
Chemist I page is loaded## Chemist Iremote type:
Onsite locations:
Lexington time type:
Full time posted on:
Posted 2 Days Agojob requisition :
10117
*** Be the First to Apply
*** Job Description Chemist IBusiness:
Pharma Solutions Department:
Analytical Quality Control (AQC)

Location:

Lexington

Job Description Business:
Pharma Solutions Department:
Analytical Quality Control (AQC)

Location:

Lexington REPORTING STRUCTURE:
This position reports to the AQC Group Lead. JOB OVERVIEW:
Reporting to the AQC Group Lead, the Chemist I performs testing of raw materials, in-process and finished products, and maintains and calibrates analytical instruments in compliance with cGMP standards.

KEY RESPONSIBILITIES:

• Perform routine/non-routine testing, both wet chemistry and instrumental analysis, according to SOPs, testing methods, protocols, compendia (USP EP/JP) etc. with minimum supervision
• Testing of raw materials, APIs, finished products, stability samples, and cleaning verification samples, etc.
• Document laboratory work according to, GDP, cGMPs, and SOPs
• Troubleshoot, calibrate and maintain instruments as required
• Prepare and label laboratory reagents, reference standards, or solutions according to SOPs.
• Write SOP's, laboratory protocols and reports, memos and/or other interdepartmental correspondence
• Participate in laboratory investigations
• Perform peer review of analytical documentation
• Follow safety procedures when working in laboratory.
• Understand and comply with cGMPs and other regulations
• Maintain the laboratory in an organized and neat manner
• Act as backup for Material sampling activities.
• Purchasing of laboratory reagents and consumables

QUALIFICATIONS:

• Bachelor of Science in Chemistry, Pharmaceutical Science, or other closely related scientific field
• Minimum 1-year hands-on experience performing quality control work within a laboratory, proficiency with HPLC/GC analysis strongly preferred
• Experience working with potent, cytotoxic materials and parenteral drug products preferred
• High level of proficiency operating all Microsoft Office applications
• Excellent communication skills, both verbally and in writing
• Detail oriented and organized
• Demonstrated ability to work within a team environment, supporting a continuous operation manufacturing facility
• Excellent problem solving, communication, and interpersonal skills
• Ability to follow written instructions

Full time remote type:
Onsite locations:
Lexington time type:
Full time posted on:
Posted 2 Days Ago### Get In Touch Introduce yourself to our recruiters and we'll get in touch if there's a role that seems like a good match.

PPL provides equal employment opportunities to all employees and applicants for employment. It prohibits discrimination and harassment based on race, color, age, sex, religion, national origin or ethnicity, disability status, genetics, protected veteran status, sexual orientation, gender identity, or expression, or any other characteristic protected by applicable law.

Our employment decisions are based on merit considering qualifications, skills, performance, and achievements. Equal employment opportunity applies to all terms and conditions of employment, including recruitment, selection, training, social programs, placement, promotion, demotion, compensation and benefits, transfers, terminations, and working conditions.
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