Analytical Science Manager

Joulé

Parsippany, NJ

JOB DETAILS
SALARY
$100,000–$135,000 Per Year
SKILLS
Analysis Skills, Analytical Method Validation, Best Practices, Biotech and Pharmaceutical, Change Control, Chemistry, Communication Skills, Corrective Action, Cross-Functional, Current Good Manufacturing Practice (cGMP), Document Management, Documentation, Drug Products, GMP (Good Manufacturing Practices), High Performance Liquid Chromatography (HPLC), ICH Regulations, Identify Issues, Instrumentation, Insurance Regulations, Liquid Chromatography-Mass Spectrometry (LC-MS), Multitasking, Organizational Skills, Outsourcing, Project/Program Management, QA Partner Testing Software, Quality Assurance, Regulations, Service Delivery, Standard Operating Procedures (SOP), Team Player, Technical Support, Technical Writing, Testing, Writing Skills
LOCATION
Parsippany, NJ
POSTED
Today

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.
System One is an Equal Opportunity Employer. All qualified applicants will receive consideration for employment without regard to race, color, religion, sex (including pregnancy, childbirth, or related medical conditions), sexual orientation, gender identity, age, national origin, disability, family care or medical leave status, genetic information, veteran status, marital status, or any other characteristic protected by applicable federal, state, or local law.
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Ref: #568-Clinical


About the Company

J

Joulé

With extensive scientific, clinical, and healthcare industry experience, Joulé recruiters excel at placing talent across core specialty areas:

  • Scientific staffing for hard-to-find skills

Working across every scientific discipline, Joulé places biologists, chemists, scientists, technicians and other specialists.

  • Clinical lifecycle recruiting

From research to regulations, safety to statistics, Joulé helps clients manage every stage of the clinical development lifecycle.

  • Equipment calibration, maintenance and validation

Laboratory and facility support comes with a total quality commitment backed by ISO 9001:2008 certification.

  • National healthcare recruitment

Trust Joulé’s extensive experience in physician, advanced practice provider and executive direct placement search.

COMPANY SIZE
500 to 999 employees
INDUSTRY
Biotechnology/Pharmaceuticals
WEBSITE
https://www.jouleinc.com/