Quality Associate -- Vendor Quality Management
Job
Interact Engineering LLC
Hanover, NJ (In Person)
$104,000 Salary, Full-Time
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Job Description
COMPANY OVERVIEW
Halo Pharmaceutical is a technology-focused contract manufacturing business with differentiated applications and capabilities in solid, semi-solid and liquid dosage forms, with a particular focus on controlled substances. Halo has long-standing commercial relationships with a number of major pharmaceutical companies and maintains facilities in both the United States and Canada. Our family of companies offers complete CDMO services including custom synthesis of intermediates, reference standards, drug substances and drug product manufacturing. Halo Pharma is part of Noramco. We are stronger together!OVERVIEW
The QA Associate will support Vendor Quality Management activities for aseptic fill operations within a CDMO environment. This role ensures that suppliers, contract laboratories, and service providers meet applicable regulatory requirements, internal quality standards, and client expectations. This position will partner with cross-functional teams (Quality, Manufacturing, Supply Chain, and Technical Operations) to ensure that vendor-related quality systems are effectively managed and compliant with US FDA (21 CFR Parts 210, 211, 820), EU GMP Annex 1, and ISO standards. This role is 100% on site in Whippany, NJ.ESSENTIAL FUNCTIONS KEY RESPONSIBILITIES S
- Support vendor qualification, re-qualification, and performance monitoring processes.
- Review and maintain Approved Vendor Lists (AVL) and associated vendor files.
- Assist in planning, coordination, and follow-up of vendor audits, including documentation of audit reports and tracking of CAPAs.
- Review vendor-supplied documentation such as Certificates of Analysis (CoA), quality agreements, material specifications, and technical data for compliance.
- Support drafting, negotiation, and maintenance of Quality Technical Agreements (QTA) with suppliers and service providers.
- Collaborate with internal stakeholders to ensure vendor-related issues (e.g., deviations, complaints, change controls) are addressed and resolved in a timely manner.
- Support investigations related to vendor-supplied materials, components, or services impacting aseptic operations.
- Monitor and trend vendor performance metrics and prepare periodic reports for Quality Management Review.
- Ensure adherence to aseptic quality standards in materials and services sourced for sterile operations.
- Maintain compliance with global GMP, cGMP, and client-specific requirements in all vendor quality activities.
POSITION QUALIFICATIONS EDUCATION/EXPERIENCE
- Bachelor's degree in Pharmacy, Life Sciences, Biotechnology, or related field.
- 2-4 years of experience in Quality Assurance within pharmaceutical/biologics manufacturing; experience in aseptic operations and/or CDMO environment strongly preferred.
- Familiarity with vendor management, supplier qualification, and audit processes.
- Knowledge of cGMP, EU Annex 1, FDA regulations, and
ISO 13485.
- Strong organizational, communication, and technical writing skills.
- Ability to work cross-functionally in a dynamic, fast-paced CDMO environment.
Skills & Competencies:
- Attention to detail and strong compliance mindset.
- Ability to analyze data and identify trends.
- Skilled in maintaining collaborative relationships with vendors and internal teams.
- Proactive in problem-solving and continuous improvement.
Physical Requirements:
- Primarily site-based with routine presence in classified cleanroom environments.
- May require gowning certification for Grade A/B aseptic areas.
- Occasional travel for supplier audits, training, or regulatory inspections.
Job Type:
Temporary Pay:
$50.00 per hourWork Location:
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