Search TSR Jobs

About TSR:

TSR is a relationship-based, customer-focused IT and technical services staffing company.

For over 40 years TSR, Inc. and its wholly owned subsidiary, TSR Consulting Services, have prospered in the Information Technology staffing business, earning the respect of companies both large and small with well refined candidate screening, timely placement, and a real understanding of the right skill sets required by our clients.

Mission & Vision

We do not believe in building a vision around the company but building a company around our vision, which is simply;

Every employee’s voice matters, their effort is appreciated, and their talent is rewarded.

We challenge each employee daily, to raise the bar on how we treat our consultants and candidates. For far too long in this industry, candidates have been ghosted, lied to, or placed at a client and then forgotten about. Each day our staff works tirelessly at qualifying and placing, top talent with our clients, in a compassionate and caring manner.

Not every candidate is a match for the job, but every candidate and consultant will be treated with respect and professionalism.

QA Shop Floor Specialist

Job Description

  • Location: Summit, NJ
  • Type: Contract
  • Job #74053

Our client, a leading pharmaceutical company, is hiring a QA Shop Floor Specialist on a contract basis.

Work Location

Summit, NJ

 

Summary

 

• Build and maintain relationships with Manufacturing Operations, Quality Control, Manufacturing Science & Technology, and other departments to effectively accomplish responsibilities, make improvements and resolve issues

• Perform QA shop floor activities, focused on Manufacturing Operations

• Ensure compliance with applicable procedures and production requirements

• Perform real-time review of manufacturing records. Must have strong authorship and ability to critically review investigations, interpret results and generate technical conclusions consistent with Quality risk management principles

• Directs quality initiatives that accomplish continuous improvement and enhance site quality system efficiencies

• Routinely recognizes and resolves Quality issues; Informs management of proposed solutions.

• Seeks management guidance on complex issues.

• Develops and revise procedures.

 

Knowledge & Skills:

• Must be action-oriented and skilled in decision-making, building relationships, problem-solving, conflict management, planning and organizing, resource allocation, coaching others, and analytical thinking

• Understands continuous improvement and improves efficiency and productivity within the group or project

• Builds relationships internally within and with cross-functional teams. Contributes to goals within the workgroup

• Ability to direct quality initiatives that accomplish continuous improvement and enhance site quality system efficiencies

• Possess sound knowledge of FDA-regulated cGMP Quality Manufacturing operations and processes and global cGMP requirements

• Must be skilled in planning and organizing, decision-making, and building relationships

• Knowledge of quality processes, including material disposition, material storage, and handling requirements, change control, product complaints, deviations, investigations, and CAPA management

• Able to recognize conflict and notify management with proposed recommendations for resolution.

• Possess an independent mindset. Work is self-directed

• Requires moderate direction to complete more complex tasks; completes routine tasks with little or no supervision

• Confident in making decisions for non-routine issue

• Intermediate to advanced ability to interpret results and situations and articulate recommendations for resolution

• Able to prepare written communications and communicate problems to management with clarity and accuracy

• Excellent verbal and written communication skills

 

Basic Requirements:

• High School Diploma/GED

• At least six months of experience working in a GMP Aseptic manufacturing environment

• Experience in FDA-regulated cGMP Quality Manufacturing operations and processes.

• Available for weekend and off-shift hours

 

Preferred Requirements:

• Bachelors Degree preferred

• 5 years of cGMP Quality Manufacturing operations and processes work experience.

• Quality Assurance Shop Floor Manufacturing roles/experience highly desired (Ex. Quality Operations, In-process QA, IPQA, Quality Inspectors).

 

 

Include a message to the recruiters.
Attach a resume file. Accepted file types are DOC, DOCX, PDF, HTML, and TXT.

We are uploading your application. It may take a few moments to read your resume. Please wait!