Job Description

External Manufacturing Quality Analytical Manager
Job Number: 22-00217
Be part of a company that delivers life-changing healthcare solutions. Eclaro is looking for an External Manufacturing Quality Analytical Manager for our client in New Brunswick, NJ. 
Eclaro’s client is a leader in the Biopharmaceutical Industry, providing quality, innovative, and affordable medicines that make a difference in the lives of patients all over the world. If you’re up to the challenge, then take a chance at this rewarding opportunity!
Position Overview:
  • Client has one of the most reliable supply networks and our clinical operations program is among the best and busiest anywhere.
  • We are a company that is forward thinking, a company in which diversity and inclusion are at the forefront of how we view our talent and how we work.
  • Our science is second to none and the transformation work underway will enable us to continue to lead our peer group.
  • Client External Manufacturing is looking to recruit a temporary External Manufacturing Quality Analytical Manager.
  • Management of analytical tech transfer activities across API & Drug Product in an external manufacturing environment
  • Provision of analytical expertise and troubleshooting support in the areas of APIs and intermediates, drug products, raw materials, and Pharmacopoeia requirements in an external manufacturing environment
  • Proactively manage all API & Drug Product Contract Laboratory Service (CLS) providers to Global External Manufacturing from a quality and compliance oversight perspective.
  • Engage with internal and external stakeholders to plan and manage the program for analytical method transfers from Client to CMOs or CMO to CMO.
  • Represent Global External Manufacturing as the QC laboratory subject matter expert in support of due diligence audits and for cause audits where laboratory related issues are a focus for such audits
  • Review and approve all major laboratory investigations/OOS events at CMOs & CLS providers.
  • Provide technical support to the QP and Quality Operations Managers in relation to same.
  • Review and approve analytical change control documents associated with CMOs & CLS providers
  • Facilitate and manage the communication flow to and from CMO analytical functions and global functions across Client such as Global Testing Standards, HQ
  • Reference Standards Management Team, Global Analytical Services, Global Regulatory Sciences etc.
  • Review and approve analytical method validation documentation & activities at CMOs and CLS providers to determine compliance with ICH requirements and manage remediation of gap analysis at Client or CLS
  • Provide analytical expert support for regulatory submissions
  • Prepare, approve and maintain the Quality Agreement with each CLS provider.
  • Establish and monitor an effective metrics program to measure the performance of the CLS providers.
  • Provide training to wider External Manufacturing team
Required Skills:
  • Ability to work independently and within team matrix environments
  • Thorough knowledge of worldwide regulatory GMP requirements and a working knowledge of FDA & EU GMP requirements
  • In depth knowledge of Quality Management Systems relating to laboratory operations
  • Ability to objectively critique investigation reports from third parties
  • Good knowledge of API and Drug Product processes and ability to differentiate between requirements
  • In depth knowledge and operational experience at management level in a Pharmaceutical QC laboratory
  • API and Drug Product experience
  • Strong knowledge of analytical technical transfer processes, compliance requirements and proven troubleshooting skills
  • Project Management skills are required
  • Strong technical knowledge of modern chromatographic methodologies.
  • Management of Third Party relationships (desirable)
  • A minimum of 5 years experience in a QC/QA environment is required for this role.
  • A minimum of a BSc in Chemistry or related discipline is also required together with a sound understanding of GMP & ICH guidelines.
  • The qualified candidate demonstrates characteristics of our Client BioPharma Behaviors. For more details refer to InSite Client Website/ People and Performance/Client BioPharma Behaviors.
If hired, you will enjoy the following Eclaro Benefits:
  • 401k Retirement Savings Plan administered by Merrill Lynch
  • Commuter Check Pretax Commuter Benefits
  • Eligibility to purchase Medical, Dental & Vision Insurance through Eclaro
If interested, you may contact:
June Binuya
June Binuya | LinkedIn
Equal Opportunity Employer: Eclaro values diversity and does not discriminate based on Race, Color, Religion, Sex, Sexual Orientation, Gender Identity, National Origin, Age, Genetic Information, Disability, Protected Veteran Status, or any other legally protected group status.

Application Instructions

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