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Analytical Lab Consultant


Job Location:

Myerstown, PA - USA

Monthly Salary: Not provided by the employer
Posted: 5 June 2026 (30+ days ago)
Application Deadline: 2 September 2026
Vacancies: 1 Vacancy

Job Summary

Hi

My name is Karthik Mutyala and I am a Recruitment Manager with Stark Pharma Solutions specializing in opportunities across the Pharmaceutical Biotechnology Medical Device and Life Sciences industries.

I am actively connecting with professionals for current and upcoming opportunities. If you are open to exploring new roles or would like to stay informed about relevant positions please send me your updated resume along with the best number and time to reach you.

Role: Analytical Lab Consultant

Location: Myerstown PA

Duration: 12-Month Contract (Potential Extension)

Position Overview

We are seeking an experienced Analytical Lab Consultant to support analytical testing method development and product development activities within a GMP-regulated pharmaceutical environment. This role will play a key part in executing laboratory studies supporting R&D initiatives and ensuring high-quality analytical data for solid oral dosage and controlled substance products.

The ideal candidate will have strong hands-on experience with analytical instrumentation laboratory investigations and technical documentation in a regulated setting.

Key Responsibilities

  • Perform analytical testing to support product development formulation and stability programs.
  • Conduct testing of solid oral dosage forms and controlled substance drug products.
  • Operate and troubleshoot analytical instrumentation including:
  • HPLC
  • Dissolution Systems
  • UV-Visible Spectroscopy
  • Prepare samples standards and reagents in accordance with approved procedures.
  • Execute analytical methods and support method development optimization and transfer activities.
  • Analyze interpret and document test results accurately and in compliance with GMP requirements.
  • Generate technical reports laboratory records and supporting documentation.
  • Ensure data integrity compliance and adherence to laboratory procedures and regulatory requirements.
  • Collaborate with R&D Quality and cross-functional teams to meet project timelines and deliverables.

Required Qualifications

  • Bachelors degree in Chemistry Pharmaceutical Sciences Biology or a related scientific discipline.
  • Hands-on experience with HPLC Dissolution and UV analytical techniques.
  • Experience using Empower Chromatography Data System (CDS).
  • Strong understanding of analytical laboratory operations within a GMP-regulated environment.
  • Excellent technical writing documentation and report generation skills.
  • Ability to execute laboratory protocols and validated analytical methods independently.
  • Strong attention to detail problem-solving and organizational skills.