Quality - Manager, Quality Assurance Scientist

Weil Group•Manati, PR

16h•Onsite

About The Position

This is a position for a Senior Quality Assurance Scientist, this position will not be supervising. The role entails frequent risk-based judgements, decision making, forming partnerships with operations, while remaining independent. Personnel in this role also conducts QA Batch Record Review prior to submitting to the Product Disposition group. For personnel assigned to Inspection/ Packaging, this role conducts direct work related to sampling and evaluation of samples as per finished product specifications.

Requirements

Bachelor’s degree in Science (e.g., Chemistry, Biology, Microbiology, Pharmacy), or Engineering with six (6) years of experience in a role exercising GMP responsibilities in a pharmaceutical industry.
Three-five years of practical experience in Quality Systems (e.g., Investigations, CAPA, Change Control) in a GMP manufacturing environment.
Knowledge of manufacturing operations of Parenteral Products Manufacturing.
In depth knowledge of cGMPs, FDA, EU regulations and the ability to interpret and apply them for intended use.
Problem Solving Skills
Critical Thinking Skills
Learning Capability Skills
Analytical Thinking Skills
Attention to Details in review of GMP documents (e.g., in Deviation Reports (manual/ electronic), SOPs, CAPAs, Logbooks, Reports, Batch Records).
Ability to identify what matters require to be dealt with sense of urgency; being able to work under fast-paced conditions and able to quickly identify when Subject Matter Experts and/or Senior Management must be involved.
Self-starter, with interpersonal skills and ability to interact with people at all levels.
Fully bilingual (Spanish/English) with excellent communication skills, both written and verbal.
Proficient knowledge of computer systems (Microsoft Office, etc.) and applications like Trackwise/Infinity and SAP.
Approve the sight screening test established within the Quality Assurance or Packaging Standard Operating Procedure (SOP) (only applies to current personnel, and candidates applying, to a position assigned in the Inspection and Packaging areas).

Responsibilities

Supports the site inspection readiness state by conducting routine walkthroughs through operational areas, observing practices vs procedures, interacting with operational personnel, examining selected batch and non-batch GMP documentation, partnering with Operations to ensure that GMP procedures are consistently followed.
Takes QA decisions by applying risk assessment/risk management principles to planned and unplanned events/ issues during operations, using quality/ compliance knowledge and experience, using data, ensuring compliance to GMPs, Client policies and guidelines.
Supports deviation resolution by providing timely inputs and coaching to deviation (functional area) owners. Reviews and approves Deviation Reports from QA standpoint, considering the nature (i.e., severity) of the deviation, frequency and how it was detected, as well as compliance elements (e.g., if the deviation constitutes a departure from a validated state or regulatory filing).
For personnel assigned to Inspection/ Packaging: conduct sampling, inspection, and/or evaluation of samples as per finished product specifications & procedures.
Reviews and approves procedures or other types of GMP documents (e.g., reports, specifications, Annual Product Quality Review, special protocols). The review must ensure that the documents are aligned to corporate standards, that families of procedures (of a related topic) are well connected (e.g., for Change Control, Product Inspection).
Ensures there is appropriate monitoring of storage conditions for quarantine materials and products.
While reviewing GMP documents, ensures the adequacy and quality of outputs from processes, ensures they are feasible and aligned to cGMP/compliance expectations while being practical, driving for <Right First-Time work> from his/herself and others.
Reviews and approves Manufacturing Batch Records (from all steps), supporting QA Product Disposition process.
Conducts basic data analysis, as needed to support deviation/investigations/change management/ technical evaluations, and/or other needs.
Reviews and approves Corrective and Preventive actions (CAPA’s) deliverables, ensuring they are appropriately to the deviation root cause(s) and deviation (i.e., the problem statement).
Provides key inputs and challenges proposed changes (for improvement, related to CAPAs, etc.) in partnership with the proponents, balancing the need to ensure quality/ compliance while adopting lean/ simplification principles. This may be in support of site projects, or other actions that are managed through the Change Control process and/or procedural change process.
Provides assistance to operational areas when a new significant (GMP practice) change is being implemented, helping coach personnel on the GMP principles behind the change.
For Quality-owned deviations, leads the Deviation Assessment and conducts and/or support investigations, as needed. This includes generating Investigation Reports, following industry-standard methodologies, Technical Writing, ensuring the investigation is standalone, having an appropriate breadth & depth.
Actively participates in the deviation investigation process, providing inputs, ensuring there is a systematic approach, using facts, data, technical inputs, quality/compliance considerations. Supports development of Impact Assessments and rationale for further processing.
Prepares presentations/ materials to reinforce training of GMP topics and/or learnings from events.
Delivers periodic Quality Talks, in partnership with Operations management, to communicate to Shop Floor what has been the outcome of key initiatives, deviations, investigations, changes, or emerging industry trends.
Supports site initiatives/projects, in addition to the product transfer initiatives and other assignments based on business needs.
During peaks of qualifications/ validations, supports the review and approval of related documentation.
Support Media Fills activities, ensuring that typical and atypical interventions are performed as established.
Supports the Annual Product Review process, for example, with inputs and/or analysis of quality events.
Supports departmental budget preparation activities, in addition to budget adherence through time.
Identifies opportunities for continuous improvements and leads/ support through completion, as needed.
Manages audit observations, investigations, change control and CAPAs records in applicable QMS system.
Assists management during internal and regulatory agencies inspections.