In-Process Quality Engineer II

In-Process Quality Engineer II

10 Oct 2024
Missouri, St louis, 63011 St louis USA

In-Process Quality Engineer II

Job Title In-Process Quality Engineer IIRequisition JR000014574 In-Process Quality Engineer II (Open)Location St. Louis, MOAdditional Locations Job Description Summary The In-Process Quality Engineer performs a variety of quality-related functions with the intent of providing Quality guidance and oversight of the manufacturing operations at the St. Louis Plant. The scope of the position includes responsibility in OOS investigations, CAPAs, Exceptions, Change Controls, with a focus on Customer Complaints. Serves as a technical leader in the Quality function in partnering with Manufacturing, Supply Chain, and other Quality groups.Job Description ESSENTIAL FUNCTIONS :

Manage and maintain Customer Complaints for the site

Write, review, and approve Exceptions, OOSs, CAPAs, Customer Complaints and Change Controls in a computerized system

Provide direct support for regulatory and customer inquiries/issues

Ensure appropriate responses to internal, corporate, customer and regulatory audits/inspections

Provide direct support for regulatory and customer inquiries/issues

Generate written correspondence and reports based on internal or customer requests in a timely manner

Lead and participate in Root Cause Analysis and Process Improvement Teams

Regularly use communication skills to exchange information, including technical, with other departments

Develop systems for ensuring cGMP compliance of manufacturing documentation systems, quality of documentation, and remediation of issues

Report and present trends to management groups during scheduled review periods

Follow all internal and basic cGMP guidelines for pharmaceutical operations

Perform GMP walkthroughs with production on a routine basis

Adhere to all safety rules and maintain 100% completion of all safety required training

MINIMUM REQUIREMENTS :

Education:

Bachelor of Science degree in Chemistry, Chemical Engineering, or related science is required.Experience: Minimum of 3 - 5 years of experience in Quality Assurance/Quality Control in a pharmaceutical manufacturing environment

2+ years of experience managing investigations, OOS, CAPAs and Change Controls

Demonstrated expertise in root cause analysis tools

Preferred Skills/Qualifications:

Excellent oral/written communication and leadership skills

Understanding of basic statistical principles and regulatory expectations

Proficient in Metric Stream, BPCS and TrackWise applications

Knowledge of GMPs for APIs including ICH Q7, CFR 210 and 211

Knowledge of Quality Systems

Bias toward change, management of change, and achievement of results

Ability to quickly identify, communicate and/or resolve issues

Ability to build relationships with partners

Advanced Microsoft Office and computer skills

COMPETENCIES:

Decision Quality, Managing Diversity, Learning on the Fly, Managerial Courage, Organizing, Priority Setting, Problem Solving, Drive for ResultsRELATIONSHIP WITH OTHERS: Daily interaction with Manufacturing personnel, Quality Engineers, Quality Control Labs, and Quality Management members to provide guidance to resolve issues.WORKING CONDITIONS:

10% Laboratory exposure to plant products, solvents, reagents, some of which are hazardous or potent compounds.

10% Manufacturing environment exposure including temperature, noise, chemical or potent compound exposure.

80% Office environment which requires sitting for long periods of time and computer use.

At Mallinckrodt, we know that we contribute to something that matters because we make quality products that impact patient lives. Our dynamic work environment provides unique experiences for employees to grow and develop.Invest in your own career with Mallinckrodt and let’s do something dynamic together.Mallinckrodt provides equal employment opportunities to applicants and employees without regard to race; color; gender; gender identity; sexual orientation; religions practices and observances; national origin; pregnancy, childbirth, or related medical conditions; protected veteran status; disability; or any other category protected by law.Additional information on Mallinckrodt’s hiring practices may be found by clicking (https://secure.compliance360.com/ext/ESLKi3LFkqY=)

Related jobs

Job Details

  • ID
    JC52678087
  • State
  • City
  • Full-time
  • Salary
    N/A
  • Hiring Company
    Mallinckrodt Pharmaceuticals
  • Date
    2024-10-11
  • Deadline
    2024-12-09
  • Category

Jocancy Online Job Portal by jobSearchi.