Instagram
youtube
Facebook

Chemist Ii

3+ years
Not Disclosed
10 Jan. 8, 2025
Job Description
Job Type: Full Time Education: B.Sc./M.Sc./B.Pharm/M.Pharm/Life science Skills: Causality Assessment, Clinical SAS Programming, Communication Skills, CPC Certified, GCP guidelines, ICD-10 CM Codes, CPT-Codes, HCPCS Codes, ICD-10 CM, CPT, HCPCS Coding, ICH guidelines, ICSR Case Processing, Interpersonal Skill, Labelling Assessment, MedDRA Coding, Medical Billing, Medical Coding, Medical Terminology, Narrative Writing, Research & Development, Technical Skill, Triage of ICSRs, WHO DD Coding

Job Title: Chemist II

Location: Lexington, KY, United States
Department: Analytical Quality Control (AQC)
Business: Pharma Solution


Job Overview

The Chemist II is responsible for performing complex testing of raw materials, in-process materials, and finished products, maintaining and calibrating analytical instruments in compliance with current Good Manufacturing Practices (cGMP). This position requires hands-on experience with laboratory techniques, specifically HPLC/GC analysis, and ensuring high standards for quality control within the lab.


Key Responsibilities

Analytical Testing & Instrumentation

  • Perform routine and non-routine testing, including wet chemistry and instrumental analysis, according to SOPs, testing methods, protocols, and compendia (USP EP/JP).
  • Test raw materials, APIs, finished products, stability samples, and cleaning verification samples.
  • Proficient in HPLC/GC analysis.
  • Troubleshoot, calibrate, and maintain laboratory instruments as required.

Documentation & Compliance

  • Document laboratory work in accordance with GDP, cGMP, and SOPs.
  • Prepare and label laboratory reagents, reference standards, or solutions according to SOPs.
  • Write and update SOPs, laboratory protocols, reports, memos, and other interdepartmental correspondence.
  • Initiate and resolve laboratory investigations.
  • Perform peer reviews of analytical documentation.
  • Follow safety procedures and ensure laboratory cleanliness and organization.
  • Purchase laboratory reagents and consumables.

Training & Leadership

  • Provide training and guidance to entry-level QC personnel.
  • Serve as a subject matter expert in laboratory practices.
  • Support team members and ensure adherence to laboratory best practices.

Qualifications

  • Education: Bachelor of Science in Chemistry, Pharmaceutical Science, or a closely related scientific field.
  • Experience:
    • Minimum of 3 years of hands-on experience in a quality control laboratory, with proficiency in HPLC/GC analysis.
    • Previous experience working within cGMP guidelines.
    • Experience with potent, cytotoxic materials and parenteral drug products is preferred.

Competencies

  • High proficiency with Microsoft Office applications.
  • Excellent communication skills, both verbal and written.
  • Detail-oriented and highly organized.
  • Demonstrated ability to work effectively in a team environment.
  • Strong problem-solving, communication, and interpersonal skills.
  • Ability to follow written instructions precisely and thoroughly.

About Us

Piramal Pharma Solutions (PPS) is an industry leader in contract development and manufacturing, offering end-to-end solutions across the drug lifecycle. We serve our customers through a globally integrated network, specializing in APIs, finished drug products, and biologics. Our commitment to quality and regulatory compliance ensures that we meet the highest industry standards.


Equal Employment Opportunity

Piramal Group is an Equal Employment Opportunity employer. We do not discriminate based on race, gender, religion, age, disability, or any other legally protected characteristic. We base employment decisions on qualifications, experience, and performance.


Join Our Team

If you're a skilled chemist with a passion for quality control and compliance, apply for the Chemist II position today!