Analytical Science Manager

System One Holdings, LLC

$100K — $135K *
Pharmaceuticals & Biotech
5 - 7 years of experience
Job Overview by Ladders

Qualifications

  • In-depth knowledge of HPLC, GC, LC-MS, and physical characterization techniques (XRPD, DSC).
  • Proven troubleshooting skills for complex analytical failures.
  • Comprehensive understanding of ICH guidelines, cGMP regulations, and industry standards.
  • Strong communication and collaboration abilities across global teams.
  • Organizational skills to manage multiple projects efficiently.
  • Masters degree in Chemistry, Pharmaceutical Sciences, or a related field with 5-10 years of industry experience.
  • Expertise in analytical method validation and global method transfers.

Responsibilities

  • Lead method transfers and validation for drug substances and products.
  • Author and review various GMP documents including SOPs and protocols.
  • Collaborate with Quality Assurance and Regulatory Affairs on technology transfers.
  • Support technical investigations and implement corrective actions for OOS results.
  • Act as Quality liaison and manage documents using Veeva eQMS.

Benefits

  • Health and welfare coverage options including medical, dental, and vision.
  • Access to spending accounts and life insurance options.
  • Participation in a 401(k) plan with employer contributions.
Full Job Description
Job Title: Analytical Science Manager
Location: Parsippany, NJ
Type: Direct Hire
Compensation: $100,000.00 - $135,000.00
Work Model: Hybrid - onsite and remote

Responsibilities

  • Lead analytical method transfers and validation activities for drug substance and drug products.
  • Author and review GMP documents such as SOPs, protocols, summary reports, and QMS records.
  • Partner with Quality Assurance, Regulatory Affairs, and external test sites to support technology transfers, and analytical method validations.
  • Support technical investigations for out-of-specification (OOS) results and collaborate with QA to implement corrective actions.
  • Serve as department Quality liaison and utilize Veeva eQMS to manage documents, deviations, change controls and quality events.


Requirements
  • In-depth knowledge of analytical instrumentation (HPLC, GC, LC-MS), and physical characterization techniques (XRPD, DSC).
  • Strong troubleshooting capabilities to resolve complex analytical failures and instrument issues.
  • Thorough understanding of global regulatory mandates, including ICH guidelines, cGMP regulations, and industry best practices.
  • Strong collaboration and communication skills across cross-functional and global teams.
  • Good organizational and multi-tasking skills to successfully manage completing projects.
  • Masters in Chemistry, Pharmaceutical Sciences, or related field with 5-10 years of pharmaceutical industry experience.
  • Strong expertise in analytical method validation, and global method transfers.
  • Excellent technical writing skills and ability to author regulatory documentation as required.
  • Hands-on experience with Veeva eQMS is highly preferred


System One, and its subsidiaries including Joulé and Mountain Ltd., are leaders in delivering outsourced services and workforce solutions across North America. We help clients get work done more efficiently and economically, without compromising quality. System One not only serves as a valued partner for our clients, but we offer eligible employees health and welfare benefits coverage options including medical, dental, vision, spending accounts, life insurance, voluntary plans, as well as participation in a 401(k) plan.


Ref: #568-Clinical

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