Jobs in the United States

25+ jobs

Save this search

Added 6 mins ago
AML Sanctions Analyst Senior
PNC Bank NA
United States
Assists in analyzing the implementation of enterprise wide and business unit Anti-Money Laundering (AML) and Sanctions Programs to prevent illegal, unethical, or improper business…
Added 8 mins ago
Senior Analyst, Procurement
RTX Corporation
austin, TX
Join our team as a Procurement Senior Analyst and play a critical role in managing the procurement lifecycle to support organizational goals and program objectives. In this remote role, you…
Added 17 mins ago
Security Operations Analyst
MAINE COMMUNITY COLLEGE SYSTEM
Augusta, ME
The Security Operations Analyst position is classified within the MSEA Support Services Unit range 21. Dependent on experience and qualifications, the position expects to pay in the…
Added 22 mins ago
DO
Analyst I
Department of Health Care Access and Information
CA
- $3,861 to $6,464 USD / month
Under supervision of the Supervisor, Health Facilities Construction, the Analyst I provides analytical and technical support to the Seismic Compliance Unit (SCU). Key responsibilities…
Added 25 mins ago
Analyst/Associate, Financial Solutions Group
CIBC World Markets Corp
Chicago, IL
This Analyst/Associate position is primarily focused on Fixed Income, Currency, and Commodity coverage. Under the guidance of the business leader, the individual will be responsible for…
Added 37 mins ago
Operational Security Analyst
STR
Las Vegas, NV
…align emerging technologies with operational needs. Provide unit-level operator training and technical support on behalf of customer development teams and performers, as…
Added 52 mins ago
Senior Financial Analyst, Financial Reporting
University of Iowa
IA
Join the University of Iowa as a Senior Financial Analyst, where you will perform a broad range of accounting and financial analysis responsibilities to assure effective and compliant…
Added 55 mins ago
CC
Analyst I / Analyst II - Psychiatric Inpatient Program (PIP) Mental Health Admin Staff - San Quentin
California Correctional Health Care Services
CA
- $6,031 to $7,547 USD / month
Effective July 1, 2025, in accordance with the applicable Memorandum of Understanding, the Personal Leave Program 2025 (PLP 2025) was implemented in response to the status of the State…
Added 1 hour ago
IT
Business Analyst III (6371)
itD Tech
Sunnyvale, CA
- $30 to $33 USD / hour
itD is seeking a Business Analyst III – Supply Planning Enablement to support workforce planning operations and execute an AI-driven automation roadmap for a global outsourced operation.…
Added 1 hour ago
CS
Senior Health Unit Analyst
CA State Lottery
CA
- $6,623 to $8,290 USD / month
Under the general direction of the Supervisor I, Health (Medical Leave Management) Unit Supervisor, the Analyst III serves as the lead analyst and technical expert for the Health (Medical…
Added 1 hour ago
Claims Reimbursement Analyst II (Health Plan Claims & Facets Experience)
CareSource Management Services LLC
Remote, United States
The Claims Reimbursement Analyst II is responsible for performing reimbursement analysis to support accurate claims payment, contract compliance, and operational efficiency. This role…
Added 1 hour ago
SO
Youth Services Specialist I - Zebulon Pike Youth Services Center- Colorado Springs
State of Colorado
Colorado Springs, CO
- $27.92 USD / hour
…leisure activities of youth, in accordance with the living unit master schedule, shift supervisor and/or other administrative direction. Provide corrective cognitive, emotional or…
Added 1 hour ago
Senior Technical Business Analyst - Information Technology
United Airlines
Chicago, IL
Possess expertise in the customer area he/she supports and has technical understanding of the business unit’s systems, capabilities, and respective technologies
Added 1 hour ago
Management and Program Analyst
U.S. Coast Guard
Washington, DC
Added 1 hour ago
MDL IT Programmer Analyst Supervisor
State of Maryland
MD
The purpose of the IT Programmer Analyst Lead is to provide
Added 1 hour ago
Property Manager
Ai Signal Research Inc
Huntsville, AL
…Logistics, Operations, Finance, Personnel/Human Resource Management, Program Management, Process Improvement, Safety, Security, and Environmental specialties; or an Associate's Degree and…
Added 1 hour ago
KC
Principal Legislative Analyst (Land Use) -King County Council
King County
Seattle, WA
- $146,722.99 to $186,814.58 USD / year
The Metropolitan King County Council is seeking a Principal Legislative Analyst with primary policy areas of growth management, land use, comprehensive planning, and regional planning. This…
Added 1 hour ago
KC
Legislative Analyst - King County Council
King County
Seattle, WA
- $115,085.36 to $146,712.18 USD / year
…to join its central policy staff in the role of Legislative Analyst. The Council's policy team conducts quantitative and qualitative analyses of legislation and policy issues, including…
Added 1 hour ago
DO
Senior Legal Analyst
Department of Education
CA
- $6,330 to $7,929 USD / month
…enthusiastic, self-motivated individual to join our team, and support the work of the Legal Support Services Office in the Legal, Audits and Charters…
Added 1 hour ago
CI
Financial Analyst
Christensen, Inc.
Salt Lake City, UT
- $65,000 to $80,000 USD / year
…they interact with management, project team leaders, business unit and department managers. This position reports to the Divisional Controller in the Finance…
Added 1 hour ago
Assistant/Associate Director of Athletics | I02592
Slippery Rock University
PA
…administrative leadership, operational coordination, and strategic support for the University’s intercollegiate athletics program. The Assistant/Associate Director reports to the Director…
Added 2 hours ago
PW
Senior Health Care Fiscal Analyst
People With Developmental Disabilities, Office for
Albany, NY
- $69,964 to $88,970 USD / year
…firm. CARS also maintains OPWDD's Cost Allocation Plan (CAP) to support reimbursement of costs associated with administering OPWDD's service delivery system of both state-operated and over…
Added 2 hours ago
AML Sanctions Analyst Senior
PNC
Remote, United States
Assists in analyzing the implementation of enterprise wide and business unit Anti-Money Laundering (AML) and Sanctions Programs to prevent illegal, unethical, or improper business…
Added 2 hours ago
Logistics Analyst II
Caladwich Consulting LLC
Quantico, VA
The Logistics (Log.) Analyst personnel will perform logistics support services in support of the Customer Supply Center (CSC)’s 4th Party Logistics (4PL) Program. The 4PL program offers…
Added 2 hours ago
Senior Financial Analyst (Job ID:4667)
Valkyrie
Virginia Beach, VA
Assist with the monthly and quarterly forecast process, consolidating inputs from program managers and business unit leaders into a company-wide outlook.

PPL Healthcare LLC

Stability Program Supervisor

United States

Apply About employer

Applications open in a new tab.

Job details

Experience: Minimum 5 years of pharmaceutical, biotechnology, or CDMO Quality Control experience, including direct stability-program experience in a cGMP laboratory.
Posting language: English
Posted: Nov 2, 2026

Original job description

Be the First to Apply

Division Piramal Pharma SolutionsPiramal Pharma Solutions is a contract development and manufacturing organization (CDMO), offering end-to-end development and manufacturing solutions across the drug life cycle. We serve our clients through a globally integrated network of facilities in North America, Europe and Asia. This enables us to offer a comprehensive range of services including Drug Discovery Solutions, Process & Pharmaceutical Development services, Clinical Trial Supplies, Commercial supply of APIs and Finished dosage forms. We also offer specialized services like development and manufacture of Highly Potent APIs and Antibody Drug Conjugation. Our capability as an integrated service provider & experience with various technologies enables us to serve Innovator and Generic companies worldwide. For more details, please visit : www.piramalpharmasolutions.com Job Title Stability Program SupervisorJob Description The Stability Program Supervisor leads the compliant and timely execution of the site Stability Program, including study initiation, sample management, chamber storage, scheduled pulls, testing coordination, data review, trending, investigations, reporting, and study closure. Reporting to the Associate Director, QC Laboratory, this role supervises Stability personnel, coordinates cross-functional execution, maintains inspection readiness, and ensures regulatory and customer commitments are achieved.Core Responsibilities Stability Program Execution

Own day-to-day execution of the site Stability Program in accordance with approved procedures, protocols, specifications, quality agreements, and applicable regulatory requirements.
Maintain the Master Stability Schedule for study initiation, sample placement, pull dates, testing, review, reporting, and closure.
Oversee sample receipt, reconciliation, labeling, storage, inventory, retrieval, transfer, and disposition with complete traceability.
Ensure stability pulls and testing are initiated and completed within required timelines and aligned with approved conditions, packaging configurations, test requirements, frequencies, and durations.
Own day-to-day execution of the site Stability Program in accordance with approved procedures, protocols, specifications, quality agreements, and applicable regulatory requirements.
Maintain the Master Stability Schedule for study initiation, sample placement, pull dates, testing, review, reporting, and closure.
Oversee sample receipt, reconciliation, labeling, storage, inventory, retrieval, transfer, and disposition with complete traceability.
Ensure stability pulls and testing are initiated and completed within required timelines and aligned with approved conditions, packaging configurations, test requirements, frequencies, and durations.
Coordinate commercial, registration, validation, commitment, annual, investigational, and customer-specific studies, as applicable.

Planning, Coordination & Delivery

Translate stability requirements into weekly and monthly plans aligned with QC Chemistry and Microbiology capacity.
Confirm analyst, instrument, method, reference standard, column, reagent, and sample readiness before scheduled testing.
Prioritize work based on regulatory commitments, product risk, customer requirements, and procedural due dates.
Monitor active studies, upcoming pulls, testing status, overdue work, report deadlines, and chamber capacity; initiate recovery plans when commitments are at risk.
Translate stability requirements into weekly and monthly plans aligned with QC Chemistry and Microbiology capacity.
Confirm analyst, instrument, method, reference standard, column, reagent, and sample readiness before scheduled testing.
Prioritize work based on regulatory commitments, product risk, customer requirements, and procedural due dates.
Monitor active studies, upcoming pulls, testing status, overdue work, report deadlines, and chamber capacity; initiate recovery plans when commitments are at risk.
Escalate resource, method, instrument, chamber, sample, or schedule constraints to the Associate Director, QC Laboratory.

Data Review, Trending & Reporting

Ensure stability results are reviewed for completeness, accuracy, specification compliance, and potential adverse trends.
Oversee preparation, technical review, approval, and issuance of interim and final stability reports.
Identify and escalate OOT results, shifts, atypical results, and emerging degradation patterns.
Provide stability data and assessments for Product Quality Reviews, regulatory submissions, shelf-life evaluations, investigations, and customer requests.
Ensure stability results are reviewed for completeness, accuracy, specification compliance, and potential adverse trends.
Oversee preparation, technical review, approval, and issuance of interim and final stability reports.
Identify and escalate OOT results, shifts, atypical results, and emerging degradation patterns.
Provide stability data and assessments for Product Quality Reviews, regulatory submissions, shelf-life evaluations, investigations, and customer requests.
Maintain and communicate program metrics, including schedule adherence, testing and report timeliness, backlog, chamber utilization, investigation aging, and right-first-time performance.

Chambers, Compliance & Quality Systems

Oversee compliant use, monitoring, capacity planning, qualification, calibration, maintenance, alarm response, and contingency planning for stability chambers and controlled storage units.
Ensure chamber excursions, alarms, sample discrepancies, OOS/OOT results, deviations, and laboratory events are promptly assessed, documented, investigated, and communicated.
Lead or support scientifically sound root cause investigations and effective CAPAs, and monitor quality records through timely closure.
Ensure compliance with cGMP, data integrity expectations, applicable FDA regulations, USP requirements, ICH guidance, approved procedures, and customer quality agreements.
Oversee compliant use, monitoring, capacity planning, qualification, calibration, maintenance, alarm response, and contingency planning for stability chambers and controlled storage units.
Ensure chamber excursions, alarms, sample discrepancies, OOS/OOT results, deviations, and laboratory events are promptly assessed, documented, investigated, and communicated.
Lead or support scientifically sound root cause investigations and effective CAPAs, and monitor quality records through timely closure.
Ensure compliance with cGMP, data integrity expectations, applicable FDA regulations, USP requirements, ICH guidance, approved procedures, and customer quality agreements.
Maintain inspection readiness and support regulatory, customer, and internal audits, including responses and remediation plans.

People Leadership & Continuous Improvement

Supervise, coach, develop, and assign priorities to Stability personnel while providing clear expectations and performance feedback.
Ensure personnel are trained and qualified, with effective cross-training and backup coverage.
Promote ownership, accountability, scientific rigor, teamwork, timely escalation, and a strong quality mindset.
Use metrics and trend analysis to reduce backlog, prevent overdue work, improve predictability, and strengthen sample lifecycle, scheduling, review, and reporting processes.
Supervise, coach, develop, and assign priorities to Stability personnel while providing clear expectations and performance feedback.
Ensure personnel are trained and qualified, with effective cross-training and backup coverage.
Promote ownership, accountability, scientific rigor, teamwork, timely escalation, and a strong quality mindset.
Use metrics and trend analysis to reduce backlog, prevent overdue work, improve predictability, and strengthen sample lifecycle, scheduling, review, and reporting processes.
Support effective use and continuous improvement of LIMS, stability management systems, eQMS, and digital reporting tools.

Cross-Functional Collaboration Partner with QC Chemistry, QC Microbiology, Quality Assurance, Regulatory Affairs, Manufacturing, Planning, Technical Services, Analytical Development, Project Management, customer teams, Engineering, Metrology, and Facilities to align testing capacity, resolve risks, support investigations, maintain chambers, and deliver regulatory and customer commitments. Decision-Making & Authority

Set daily, weekly, and monthly execution priorities in alignment with QC leadership.
Assign Stability team work and coordinate testing and data-review priorities with laboratory leaders.
Initiate recovery and improvement plans, drive cross-functional follow-up, and escalate material compliance or delivery risks.
Set daily, weekly, and monthly execution priorities in alignment with QC leadership.
Assign Stability team work and coordinate testing and data-review priorities with laboratory leaders.
Initiate recovery and improvement plans, drive cross-functional follow-up, and escalate material compliance or delivery risks.
Final Quality disposition, regulatory strategy approval, and decisions requiring Quality Unit authority remain with designated functional leadership and Quality Unit approvers.

Qualifications

Bachelor's degree in Chemistry, Biology, Microbiology, Pharmaceutical Sciences, Biochemistry, or a related scientific discipline; advanced degree or relevant certification preferred.
Minimum 5 years of pharmaceutical, biotechnology, or CDMO Quality Control experience, including direct stability-program experience in a cGMP laboratory.
Experience coordinating stability studies, sample pulls, testing, data review, trending, reports, investigations, and study closure.
Prior supervisory, team-lead, or program-lead experience strongly preferred.
Working knowledge of cGMP, applicable FDA regulations, USP requirements, ICH stability guidance, data integrity, and laboratory quality systems.
Strong planning, technical writing, investigation, problem-solving, leadership, communication, and cross-functional collaboration skills.
Bachelor's degree in Chemistry, Biology, Microbiology, Pharmaceutical Sciences, Biochemistry, or a related scientific discipline; advanced degree or relevant certification preferred.
Minimum 5 years of pharmaceutical, biotechnology, or CDMO Quality Control experience, including direct stability-program experience in a cGMP laboratory.
Experience coordinating stability studies, sample pulls, testing, data review, trending, reports, investigations, and study closure.
Prior supervisory, team-lead, or program-lead experience strongly preferred.
Working knowledge of cGMP, applicable FDA regulations, USP requirements, ICH stability guidance, data integrity, and laboratory quality systems.
Strong planning, technical writing, investigation, problem-solving, leadership, communication, and cross-functional collaboration skills.
Proficiency with LIMS, stability management systems, eQMS, Microsoft Office, and applicable laboratory systems.

Measures of Success

On-time completion of stability pulls, testing, data review, reports, and regulatory or customer commitments.
Sustained control of overdue activities and backlog, with improved schedule predictability.
Timely, scientifically sound closure of investigations, deviations, CAPAs, and chamber excursions.
Accurate sample inventory, traceable documentation, effective chamber capacity management, and inspection readiness.
On-time completion of stability pulls, testing, data review, reports, and regulatory or customer commitments.
Sustained control of overdue activities and backlog, with improved schedule predictability.
Timely, scientifically sound closure of investigations, deviations, CAPAs, and chamber excursions.
Accurate sample inventory, traceable documentation, effective chamber capacity management, and inspection readiness.
Qualified personnel, resilient backup coverage, and right-first-time stability documentation and reporting.

Apply About employer

More about this job

Skills

Reporting
Inspection
Packaging
Regulatory compliance
Quality control systems
Manage quality
Internal auditing
Leadership
Process improvement
Teamwork
Scheduling
LIMS
Collaboration
Quality assurance
Regulatory affairs
Project management
Decision making
Biotechnology
Quality control
Technical writing
Problem solving
Communication skills
Microsoft Office
Documentation

Report this job