Procurement Operations Specialist

On-Board Companies; Franklin Township (NJ); In loco; USD 41.000 - 48.000; Tempo pieno

Vantaggi offerti da questo lavoro

401K

Dental insurance

Life Insurance

Medical Insurance

Vision Insurance

Descrizione del lavoro

On-Board Services, Incorporated is seeking a Procurement Operations Specialist for an on-site contract role in Somerset, NJ. You will coordinate supplier management, act as a quality liaison between R&D and suppliers, and ensure GMP compliance.

The ideal candidate holds a Bachelor’s degree and 3–5+ years in QA, vendor management, or procurement compliance in regulated settings. Knowledge of ISO 9001, AS9100, cGMP or FDA regs is preferred; ASQ CQA or Lean Six Sigma is a plus.

Competenze

• Bachelor's degree in a related field (Supply Chain, Quality Management, Life Sciences, Engineering).
• 3–5+ years in QA, vendor management, or procurement compliance in regulated industries.
• Familiarity with ISO 9001, AS9100, cGMP or FDA regulations.
• ASQ CQA or Lean Six Sigma credentials preferred.

Mansioni

• Serve as the primary operational and quality liaison between pharmaceutical manufacturing/R&D teams and external suppliers.
• Manage supplier performance metrics, conduct regular business reviews, and mitigate supply chain quality risks.
• Oversee qualification and onboarding of new raw material, API, and clinical trial suppliers.
• Lead supplier quality audits and CAPA processes.
• Maintain supplier data and audit readiness in Veeva QMS.

Conoscenze

Quality Assurance

Vendor Management

Procurement Compliance

Regulatory Knowledge

Formazione

Bachelor's degree (Supply Chain/Quality Management/Life Sciences/Engineering)

Strumenti

Veeva QMS

Descrizione del lavoro

On-Board Services is hiring a Procurement Operations Specialist

On-Board Services, Incorporated is an on-site contract service provider for a local manufacturing entity providing full time positions to our employees. We offer benefits as well as 401k.

About Us

On-Board Services, Incorporated is an on-site contract service provider for a local manufacturing entity providing full time positions to our employees. We offer benefits as well as 401k.

Position Details

• Position Type: Contract
• Job Location: Somerset, NJ
• Benefits: 401K, Dental insurance, Life Insurance, Medical Insurance, Vision Insurance
• Compensation: $30-35/ hour

Core Responsibilities

Supplier Management & Procurement

• Serve as the primary operational and quality liaison between pharmaceutical manufacturing/R&D teams and external suppliers.
• Manage supplier performance metrics, conduct regular business reviews, and mitigate supply chain quality risks.
• Oversee the qualification and onboarding process for new raw material, API, and clinical trial suppliers.
• Participate in Impact Assessments, Supplier assessment, Supplier and Material Changes Require Formal Evaluation and Supply chain tracebility form and site quality overview.

QMS & Veeva Process Ownership

• Direct and manage the full lifecycle of supplier workflows within the Veeva QMS platform along with internal and external stakeholder management.
• Ensure all supplier-related data, documentation, and history are accurately maintained and audit-ready in Veeva.

Audits & Compliance

• Partner with the QA, QC, MSAT, SCM, Production, Regulatory and other teams to coordinate, execute, and follow up on supplier quality audits.
• Ensure suppliers adhere to cGMP, FDA, EMA, and other relevant global regulatory frameworks.

Change Notifications, SCARs, and CAPAs

• Evaluate and process Supplier Change Notifications (SCNs) to assess their impact on R&D or manufacturing processes.
• Issue and track SCARs when supplier materials or services fail to meet established specifications.
• Lead root-cause analysis investigations with suppliers to develop, implement, and close out effective CAPAs.

Qualifications and Skills

• Education: Bachelor's degree in Supply Chain, Quality Management, Life Sciences, Engineering, or a related discipline.
• Experience: 3 to 5+ years of experience in quality assurance, vendor management, or procurement compliance within a regulated industry.
• Regulatory Knowledge: Familiarity with standards such as ISO 9001, AS9100, cGMP, or FDA regulations depending on the sector.
• Certifications: Preferred credentials include ASQ Certified Quality Auditor (CQA) or Lean Six Sigma.

On-Board was founded in 1976 by Robert L. Wilson to provide Engineering and Design services to the chemical manufacturing industry. Today, On-Board is a thriving privately held family of companies with services including: Consulting, Professional Engineering, Industrial Maintenance and Facility Management, Contracted Manufacturing and Production Services, as well as Temporary Staffing and Recruiting throughout North America.

The On-Board Family of Companies conducts operations through its Corporate Headquarters located in East Windsor, NJ along with Regional Offices in New Castle, DE and Wake Forest, NC. On-Board’s Mission is to provide “Flexible Service by applying the talents of our people, work processes and technology to meet our clients’ expectations in a Safe, Responsible and Dependable manner.”

On-Board Companies provides equal employment opportunities (EEO) to all employees and applicants for employment without regard to race, religion, sex, national origin, age, disability or genetics.

JD#26-01424 INDOJ