QA Specialist
Hays

Morris Plains, New Jersey

Posted in Recruitment Consultancy


This job has expired.

Job Info


The end client is unable to sponsor or transfer visas for this position; all parties authorized to work in the US without sponsorship are encouraged to apply.

Our Client is seeking a QA Specialist in Morris Plains, NJ.

Role Description

The Quality Assurance delivers on the client's commitment to bring life-changing therapies to patients through the robust QA processes and systems. Our approach is agile, innovative and collaborative and our teams are genuinely committed to the rapid delivery of safe life changing therapies. As part of the broader Pharmaceutical Development & Manufacturing (PDM) team you will be part of a team that is changing the world and helping millions of people live healthier, more fulfilling lives.

The Quality Assurance on the floor is responsible for coordinating, managing on the floor Quality Oversight within commercial Drug Product operations to ensure sustained compliance with GMPs and regulatory readiness.

• Provides Quality oversight to operations on the shop floor. Supports manufacturing operations (upstream and downstream) at real time.
• Assists and advises on pertinent quality issues as they arise during plant operations.
• Troubleshoot and elevate noncompliance issues and events observed.
• Demonstrates knowledge of investigation, CAPA, and corrective action processes.
• Demonstrates ability to effectively prioritize and manage multiple project workloads
• Ensures compliance to policies and procedures
• Maintains and supports material inventory, status and transfers.
• Performs and supports changeovers in production area as required.
• Participates in audits and other projects as appropriate.
• Supports manufacturing operations (upstream and downstream) and staff as needed to identify and address product quality and compliance issues as they arise.
• Reviews documentation associated with production operations. Ensures adequate levels of documentation are acceptable and compliant to existing procedures.
• Participates in process improvement initiatives targeting for Right First Time (RFT) on documentation.
• Participates in activities associated with event resolution and CAPAs, with a focus on organizing and attending cross-functional meetings.
• Implements and ensures adherence of appropriate regulations and quality standards.
• Supports operations to encourage a Quality Culture and ensure a safe working environment.
• Completes job-related training as required.

Skills & Requirements

• 2+ years of relevant experience in a GMP environment related field and a BS OR 3+ years of relevant experience and an AA degree.
• Prior experience in pharmaceutical industry is preferred.

Why Hays?

You will be working with a professional recruiter who has intimate knowledge of the Information Technology industry and market trends . Your Hays recruiter will lead you through a thorough screening process in order to understand your skills, experience, needs, and drivers. You will also get support on resume writing, interview tips, and career planning, so when there's a position you really want, you're fully prepared to get it.

Additionally, this position is a contract role where Hays offers you the opportunity to enroll in full medical, dental or vision benefits.

• Medical
• Dental
• Vision
• 401K
• Life Insurance ($20,000 benefit)

Nervous about an upcoming interview? Unsure how to write a new resume?

Visit the Hays Career Advice section to learn top tips to help you stand out from the crowd when job hunting.

Hays is an Equal Opportunity Employer.

Drug testing may be required; please contact a recruiter for more information. #1126855


This job has expired.

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