Sr In-Process Quality Eng

Posted 14 Days Ago
Be an Early Applicant
Fenton, MO
5-7 Years Experience
Healthtech • Pharmaceutical • Manufacturing
The Role
The Senior Quality Engineer performs quality-related functions to provide support to manufacturing operations, including batch record review, investigations, CAPA's, change controls, supplier quality, and validation. They ensure compliance with internal and regulatory guidelines in a pharmaceutical manufacturing environment.
Summary Generated by Built In

Job Title

Sr In-Process Quality Eng

Requisition

JR000014450 Sr In-Process Quality Eng (Open)

Location

Fenton, MO

Additional Locations

St. Louis, MO

Job Description Summary

Job Description

SUMMARY OF POSITION:

The Senior Quality Engineer performs a variety of quality-related functions with the intent of providing Quality support to manufacturing operations at the Fenton Manufacturing Plant. This will include new manufacturing processes that are transferred to the site. The scope of the position includes manufacturing batch record review, manufacturing and quality investigations, CAPA’s, change controls, supplier quality and validation.
 

ESSENTIAL FUNCTIONS:

Execute batch record review and document deficiencies
Identify exceptions and report exceptions
Resolve documentation discrepancies and issues with manufacturing operations personnel in a timely manner to allow for material release
Execute line clearances
Perform batch record accountability
Create and/or revise Quality related SOPs
Review and approve exceptions, change controls and CAPAs in the Trackwise module.
Review of data for release APIs, Excipients, and Finished Bulk Product
Perform supplier qualification activities including desk audits and supplier approvals
Author and/or review validation documentation including equipment qualification and process validation
Participate in, or Lead Root Cause Analysis teams
Follow all internal and basic cGMP guidelines for pharmaceutical operations
Adhere to all safety rules and maintain 100% completion of all safety required training
Maintain Compliance Wire training
 

MINIMUM REQUIREMENTS:

Education:

BS in Chemistry, Biology, related science or equivalent combination of education, experience, and competencies

Experience:

Minimum of 5-7 years' experience in Quality Assurance in a pharmaceutical manufacturing environment

Preferred Skills/Qualifications:

Excellent communication and leadership skills
Knowledge of GMP's for Dosage Products
Knowledge of Supplier Quality or Validation Principles
Understanding of basic statistical principles, and regulatory expectations
Knowledge of Quality Systems
Ability to quickly identify, communicate and/or resolve issues
Ability to build relationships with partners
Good verbal and written communication skills

COMPETENCIES:

Dealing with ambiguity, approachability, decision quality, functional/technical skills, integrity and trust. Customer Focus, managing diversity, fairness, managing and measuring work, motivating others.

RELATIONSHIPS WITH OTHERS:

Reports directly to the Plant Quality Manager. Daily interaction with Manufacturing personnel, Focus Factory Managers, and Quality Management members to provide guidance to resolve issues.
 

WORKING CONDITIONS:

20% Laboratory exposure to plant products, solvents and reagents, some of which are hazardous or potent compounds
80% office environment which includes sitting for long periods of time and computer use.

DISCLAIMER:

The above statements are intended to describe the general nature and level of work being performed by employees assigned to this classification.  They are not intended to be construed as an exhaustive list of all responsibilities, duties, and skills required of employees assigned to this position.

The Company
Bridgewater, NJ
3,383 Employees
On-site Workplace
Year Founded: 1867

What We Do

At Mallinckrodt, we use strategic vision and employee-driven momentum to pursue a powerful mission: Listening for needs and delivering solutions.

As a leader in specialty pharmaceuticals, we develop, manufacture, market and distribute innovative treatments for underserved patient populations within neurology, rheumatology, hepatology, nephrology, pulmonology, ophthalmology, and oncology; immunotherapy and neonatal respiratory critical care therapies; analgesics; cultured skin substitutes and gastrointestinal products. . Our expertise also extends into acute and critical care hospital products, as well as our broad portfolio of generic prescription medicines and active pharmaceutical ingredients.

Together, we’re helping shape the future of the specialty pharmaceuticals industry by leveraging the values our founders instilled over 155 years ago – quality, integrity and service.

To learn more about Mallinckrodt, visit www.mallinckrodt.com.

Equal Opportunity Employer
Mallinckrodt Pharmaceuticals provides equal employment opportunities (EEO) to all employees and applicants for employment without regard to race, color, religion, gender, sexual orientation, gender identity, national origin, age, disability, veteran status or genetics. In addition to federal law requirements, Mallinckrodt Pharmaceuticals complies with applicable state and local laws governing nondiscrimination in employment in every location in which the company has facilities. This policy applies to all terms and conditions of employment, including recruiting, hiring, placement, promotion, termination, layoff, recall, transfer, leaves of absence, compensation and training.

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