Sr. Operations Quality Engineer

At Par Health, we believe great healthcare is built on getting the essentials right. We’re looking for passionate, talented individuals who share our commitment to improving lives. With 4,000+ team members worldwide, we lead with pride and purpose—prioritizing quality and safety while fostering a culture of continuous improvement, accountability, and teamwork. Elevating the Essentials isn’t just our tagline, it’s the higher standard we live by every day.
** Job Description Summary
** The Sr. Quality Engineer has responsibility for interpreting and applying the applicable regulations and Quality Systems, and developing and implementing standard operating procedures (SOPs) and policies. In a cGMP manufacturing setting, provide Process / Quality Engineering support to all areas of the facility to ensure delivery of the highest quality product to the customer. The Sr. Quality Engineer will provide statistical and process support to assist with continuous improvement activities.
** Job Description
**** ESSENTIAL FUNCTIONS****:
** The role provides input into regulatory filings as well as guidance for the various elements of the Quality System, including but not limited to the following:  Validation, Deviations (Exceptions), Supplier Quality,  Product complaints, Internal Audits, OOS, CAPA, Annual Product Review, Process control, Change Control,  and identification/ recommendations for continuous improvement opportunities (internal/external).  The Sr. Quality Engineer applies the appropriate statistical tools to analyze data, identify root cause and develop corrective actions for effective problem resolution of moderate to difficult scope and complexity.

Additional functional requirements:
* Acts as SME for validation activities.  Provides validation guidance and support for computer systems, production processes, and both production and laboratory equipment.
* Acts as lead for Quality Systems ownership for day to day activities and monthly metrics and trending.
* Provides guidance and training to Quality Department personnel in all applicable Quality Systems.
* Leads compliance efforts for the site.
* Provides direction and leadership for quality system improvements and for benchmarking of other sites to establish and implement best practices.
* Participates in continuous improvement activities as required.  May lead continuous improvement activities (e.g. kaizen).
* Works within production teams, develop data trending models using appropriate statistical methods and deploy use of them.
* Analyzes trends related to various activities and identify root causes and areas for improvement.  Utilizes output of trend analysis to initiate investigations and or corrective/preventive action projects.
* Assesses manufacturing and support processes to identify and implement quality minded efficiencies and improvements.
* Leads or participates in risk analysis activities (FMEA) for changes to production or design processes. Uses process mapping tools to define critical control points and recommend alternatives to reduce risk of defects.
* Oversees cross functional teams for complaint investigation and resolution.  Generates final complaint investigation reports.
* Leads investigation efforts and accurately document investigation plans, supporting data, and conclusions.
* Leads corrective and preventive action projects.
* Participates on extended core teams as a QA representative.
* Statistical analysis (Excel, Mini-tab, other statistical software).
* Develops sampling plans, as needed.
* Provides change management guidance and support.
* Provides internal / external audit support.  May assume the Lead Auditor role.
* Serves as a subject matter expert for Regulatory and Customer audits.
* Conduct New Employee orientation.
* Provides supplier quality oversight, including technical support for supplier selection and supplier quality evaluations as well as the development and management of supplier corrective action plans. Work closely with suppliers to ensure quality expectations and strengthen supplier relationships.
** DEPARTMENT SPECIFIC/NON
- ESSENTIAL FUNCTIONS:

*** Other duties as assigned with or without accommodation.
* Participates in a certified 5S Workplace System to ensure good housekeeping and organization.
* Prioritizes and plans workload and team assignments to meet all internal and external customer needs for maximum efficiency and accuracy.
* Effectively trains others in a positive manner.
** MINIMUM REQUIREMENTS****:
**
* Education:

* B.S. degree in Engineering or Science or a related field

* Experience:

* Minimum of 5 years’ experience in QA/pharmaceutical manufacturing environment
* Preferred Skills/

Qualifications:

** Other Skills/

Competencies:

* Knowledge of regulations associated with ICH Guidelines (Q7, Q8, Q9, and Q10), FDA, EMA, USP, EP, and JP.Direct interactions with regulatory inspections.

Strong technical, oral, and written communication skills.

Able to speak, read, and write the English language.

Knowledge of Six Sigma Tools or…