Pharma Procurement & Quality Ops 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

For immediate consideration please send your resume to [e-mail]
Subject Line: Position Title and State you are Located .

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

The Procurement Operations Specialist oversees the end-to-end lifecycle of R&D and manufacturing suppliers. This role balances strategic procurement (supplier management, onboarding, performance) with strict quality compliance. The candidate will act as the primary owner of the Veeva Quality Management System (QMS) workflow for external vendors, driving audits, change controls, deviations, Supplier Corrective Action Requests (SCARs), and Corrective and Preventive Actions (CAPAs). A Procurement Operations Specialist ensures that an organization's purchasing activities, vendor materials, and supplier networks meet internal quality standards and external regulatory requirements.

Core Responsibilities
1. 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.
2. 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.
3. 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.
4. 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.

Apply Today!
www.onboardusa.com

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.


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