Quality Control Sr Analyst

Piramal Pharma Ltd•Sellersville, PA

18h•Onsite

About The Position

The Senior Quality Specialist, Laboratory Investigations & Data Integrity is an experienced Quality Control individual contributor responsible for leading and completing laboratory investigations, OOS/OOT assessments, CAPA development, and comprehensive review of analytical data in a cGMP pharmaceutical laboratory. Reporting to the Associate Director, Quality Control, the role applies scientific and regulatory judgment to determine root cause, assess product and data impact, document defensible conclusions, and drive timely actions to closure. The position builds on the Senior QC Analyst technical foundation and retains the ability to understand and evaluate analytical testing of raw materials, finished products, stability samples, and special-request samples. The specialist independently reviews paper and electronic laboratory records, chromatographic data, calculations, metadata, audit trails, instrument outputs, and LIMS entries to verify completeness, accuracy, traceability, procedural compliance, and data integrity. • Regulatory and corporate requirements: Adhere to applicable FDA requirements and guidance, 21 CFR Parts 210, 211, and 11 as applicable, USP/EP compendial requirements, ICH guidance, approved site procedures, and corporate Quality, safety, health, and environmental policies. • Values: Consistently demonstrate integrity, scientific rigor, transparency, ownership, respectful challenge, and Piramal Pharma Solutions standards of ethical conduct.

Requirements

Bachelor’s degree in Chemistry, Analytical Chemistry, Pharmaceutical Sciences, Biology, Microbiology, or a related scientific discipline is required.
Minimum five (5) years of pharmaceutical Quality Control laboratory experience in a GMP-regulated environment, including independent analytical testing and data review.
Demonstrated experience authoring or leading laboratory investigations, including OOS/OOT assessments, hypothesis testing, root-cause analysis, product-impact evaluation, CAPA development, and effectiveness verification.
Hands-on experience with HPLC and applicable techniques such as GC, dissolution, UV-Vis, FTIR, Karl Fischer, pH, particle-size analysis, XRD, wet chemistry, titration, viscosity, conductivity, or other compendial testing.
Demonstrated ability to review electronic raw data, metadata, chromatographic processing, audit trails, LIMS records, and hybrid records in accordance with ALCOA+ and cGMP data-integrity expectations.
Strong working knowledge of FDA OOS and data-integrity guidance, 21 CFR Parts 210 and 211, 21 CFR Part 11 as applicable, USP/EP requirements, Good Documentation Practices, and scientifically sound investigation principles.
Advanced scientific investigation, critical-thinking, root-cause analysis, and technical-writing capability.
High attention to detail and ability to critically review complex paper and electronic analytical records.
Sound, independent Quality judgment with willingness to question unsupported conclusions and escalate risk.
Ability to separate facts, observations, hypotheses, and conclusions and communicate each clearly.
Strong knowledge of chromatography, laboratory controls, OOS/OOT principles, CAPA systems, and data-integrity expectations.
Ability to influence and coordinate analysts, laboratory leadership, QA, IT, validation, and cross-functional SMEs without direct authority.
Strong organization, prioritization, and follow-through across multiple time-sensitive investigations and reviews.
Clear written, verbal, presentation, and inspection-interaction skills.
Commitment to transparent reporting, patient and product protection, and an open Quality culture.

Nice To Haves

An advanced scientific degree is preferred.
Experience with laboratory systems such as LIMS, chromatography data systems, electronic QMS, SAP, instrument software, or comparable platforms is preferred.
Experience supporting multiple products, customers, methods, and concurrent priorities in a CDMO/CMO environment is preferred.

Responsibilities

Lead, author, coordinate, and complete laboratory investigations involving OOS, OOT, atypical, invalid, questionable, or unexpected results and laboratory-related deviations.
Conduct and document prompt laboratory assessments that evaluate analyst execution, calculations, sample and standard preparation, reagents and solutions, method requirements, instrument condition, system suitability, chromatograms, integration, processing parameters, environmental conditions, maintenance, calibration, and other relevant laboratory controls.
Coordinate with QA, Manufacturing, Technical Services, Regulatory Affairs, and other functions to support an expanded investigation of manufacturing, sampling, materials, methods, and prior history.
Maintain active oversight of assigned OOS/OOT records from initiation through closure.
Apply structured root-cause tools and scientific critical thinking to distinguish assignable cause, contributing factors, systemic causes, method variability, instrument or system issues, sampling issues, and potential manufacturing causes.
Develop risk-based corrective and preventive actions that address confirmed root and contributing causes.
Perform independent, comprehensive review of raw data and reported results for routine, release, stability, validation, transfer, and investigation testing.
Review complete electronic records, relevant metadata, sequence information, processing histories, audit trails, deleted or aborted injections, reinjections, reprocessing, reintegration, manual entries, date and time information, user actions, and unexplained or unreported data.
Apply ALCOA+ principles to paper, electronic, and hybrid laboratory records.
Execute and document risk-based audit-trail reviews for applicable laboratory systems.
Partner with QC management, QA, IT, validation, metrology, and system owners to evaluate laboratory computerized systems, user access, segregation of duties, time synchronization, method and processing controls, data paths, interfaces, backup and archival arrangements, and system limitations.
Use advanced knowledge of HPLC and other laboratory technologies to assess method execution and performance.
Trend OOS/OOT events, invalidations, repeat testing, reintegration, analyst and instrument factors, recurring root causes, CAPA effectiveness, aging, and investigation cycle time.
Author or revise procedures, investigation templates, checklists, decision trees, data-review tools, and training materials.
Train and mentor analysts, reviewers, and investigators on OOS/OOT requirements, investigation documentation, hypothesis testing, root-cause analysis, CAPA quality, Good Documentation Practices, electronic data review, audit trails, and data-integrity expectations.
Maintain investigation and data-review records in an inspection-ready state.
Provide clear, factual, and timely updates to the Associate Director QC, QA, project teams, and other stakeholders.
As business needs require and within current qualification, perform or support analytical testing, standards and sample preparation, LIMS documentation, peer review, protocol and report preparation, and laboratory troubleshooting in accordance with approved methods and procedures.
Independently prioritize multiple investigations, reviews, CAPAs, and improvement activities.