Stability Scientist at Eclaro

New Brunswick, NJ

About the Job

Stability Scientist
Job Number: 24-01238

Be part of a company that delivers life - changing healthcare solutions. Eclaro is looking for a Stability Scientist for our client in New Brunswick, NJ.

Eclaro’s client is among the world’s largest pharmaceutical companies, trusted by billions to provide superior, cutting-edge, and inexpensive medicine that improves health and well-being. If you’re up to the challenge, then take a chance at this rewarding opportunity!

Position Overview:

Responsible for stability product strategy and oversight of product stability programs for commercial small molecules Drug Substances and Drug Products Oral and Sterile.
Activities include those associated with product stability strategy, stability program requirements, authoring / approving stability protocols, and preparation, review and approval of stability reports and regulatory filings.

Responsibilities:

Accountable for the stability program on assigned brand (s) and acts as Stability Product Lead.
Participates on transfer team for new products to internal and external sites (as required), reviews registrational stability studies and conducts gap analysis against Global Manufacturing & Supply requirements. Develops stability data where gaps exist.
Develops and maintains expertise on the overall stability performance of products manufactured in the global supply chain, including maintaining a working knowledge of the attributes that impact the products’ performance/stability profile
Serves as stability representative on project teams covering post-approval changes, designs and executes required premarket stability program in support of the change
Perform change control impact assessments and document the stability assessment in change controls.
Review and endorse change controls as an expanded reviewer. Initiate change controls related to stability operations
Provide the technical requirements in a Master Stability Protocol, review and approve study specific protocols and /or batch enrollment forms
Responsible for the handling of annual commercial stability program for assigned products in coordination with sample management groups.
Authors stability sections of CTD dossiers for post-approval filings, annual reports, product renewals, Annual
Product Stability Reviews, and stability related responses to health authority inquiries.
Serves as stability representative for OOT/OOS investigations, Market Action Fact Finding, and other investigations related to potential quality issues and/or deviations from standards.
Leads work activities involving Change Controls and CAPA’s .
Identify information regarding stability program that may impact lab capacity, product studies or regulatory commitments directly, escalate promptly to management and act as required.
Responsible for stability procedures and ensures consistency with site department and Client groups procedures.
Participate and/or lead OpEx initiatives to streamline and standardize management of stability programs
Support health authorities inspection internal and external.
Represents department in cross functional projects
Ensure training requirements are met.
Acts as an advisor and mentor to stability staff

Required Qualifications:

B.S. Chemistry, Biology, Microbiology or relevant discipline
8 years of relevant work experience required, preferable in a Pharmaceutical environment.
Experience with authorship and able to critically review investigations, interpret results, and generate technical conclusions consistent with Quality management principles
Experience to oversee external service providers involved in stability studies.

Required Skills:

Expert knowledge and understanding of stability ICH Guidelines (Q1A, Q5C) and associated policies, directives and guidance documents.
A thorough knowledge of cGMP regulations as referenced in The Code of Federal Regulations (21CFR) and their specific application to stability programs in a pharmaceutical manufacturing facility.
Expert Knowledge of US/EU/ROW Requirements, Corporate Directives and industry best practices.
Knowledge of Drug Substance and Drug Product manufacturing and good understanding of analytical and/or Microbiology methods.
Very good skills to drive development of technical or scientific initiatives for solving complex problems/issues; recommending and drive science-based decisions/ implementation of solutions.
Good Knowledge of evaluation and interpretation of stability data using statistics software. Review data and demonstrated ability to recognize anomalous trends or results
Significant experience on health authorities inspections on stability programs.
Excellent written and verbal communication skills
Exhibit strong leadership and decision making skills.
Advanced ability to work independently and collaboratively in a team matrix environment, contribute to a team based environment, promoting a high commitment to business goals and objectives.
Advanced ability to prioritize objectives from multiple projects and ability to adapt to quick changes in schedules in order to accommodate priority requests.
Advanced knowledge of Microsoft Office applications, LIMS, Quality
Management system (e.g. TrackWise or Veeva), Statistics software (e.g. SlimSTAT, JMP).

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:
Paul Quibuyen
Christian.Quibuyen@eclaro.com
6466952942
Paul Quibuyen | 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.