Quality Analyst

Hybrid in Titusville, NJ, US • Posted 1 day ago • Updated 1 day ago
Contract W2
5 Months
No Travel Required
Hybrid
$34 - $39/hr
Fitment

Dice Job Match Score™

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Job Details

Skills

  • Change Control
  • Data Analysis
  • Document Management
  • QMS
  • COMET
  • VIVA
  • VIVA VAULT
  • DEA
  • Compliance
  • Quality Assurance
  • QA

Summary

Title: Quality Analyst

Duration: 09/21/2026 to 01/29/2027 (Possibility of Extension)

Location: Titusville, NJ 08560 OR Horsham, PA 19044 (Hybrid)

 

Pay Rate: $39.12/hr

 

NOTES FROM MANAGER:

- Role will be HYBRID, 3 days onsite, can be onsite in Titusville, NJ or Horsham, PA

- Bachelor’s degree is required

- Must have at least 2-5 years of relevant exp.

- Must have Regulations knowledge

- DEA Regulations knowledge as well

- Experience with COMET system, or some type of Quality Mgmt. System (QMS)

- Must have prior Compliance exp.

 

Top 3 Skills:

- Data analytics exp.

- Computer skills

- Background in Quality or Compliance

 

Job Description:

The overall purpose of this position is to support quality activities for Commerical Quality including controlled substance requirements, quality complaints, change control, documentation, internal audit/ supplier audits. Adheres to environmental policy, procedures, and supports department environmental objectives.

 

Essential duties and responsibilities:

• Process Know Your Customer applications to purchase a specific product (50%)

• Conduct routine data analysis for Suspicious Order Monitoring. (10%)

• Process day-to-day product quality complaint (PQC) in quality system including evaluating PQC, assigning investigation, conducting investigation, writing investigation summary. Proactively manage PQCs workflow with stakeholders to ensure all investigations are completed in a timely manner. (10%)

• Process day-to-day quality events and change control records in COMET system (10%)

• Coordinate documents and procedures in truVault system and any other document management system.(10%)

• Coordinate internal and/or supplier audits including setting up logistic / preparation for the audits, drafting audit plan, supporting audit execution, coordinating audit response and CAPA with stakeholders, creating and documenting audit records in system. Ensure all audit commitments are delivered on time (10%)

 

Required: BA/BS – Technical / Life Science

Desirable: MA/MS/MBA – Business / Technical /Life Science

Support Quality and Compliance Initiatives from Enterprise Quality and/or Global Business Quality

 

Essential knowledge and skills

Knowledge

• 2-5 years’ experience in the Pharmaceutical or related industry;

• Up-to-date knowledge of relevant pharmaceutical legislation and GMP / GDP;

• Up-to-date knowledge of DEA regulations

• Experience working in the quality organization.

 

Skills

• Highly experienced in COMET system, generating query and report, and data analysis with excel spreadsheet

• Results-driven leader who commits to stretch goals and delivers results.

• Ability to build and nurture strong, positive relationships with business partners in IT, Manufacturing, Regulatory Affairs, Commercial and Quality functional groups.

• Demonstrated understanding of regulatory requirements that impact Market Quality specifically, and client's more broadly. Experience in dealing with regulatory inspections and inspectional requirements

 

Core competencies required for this role:

Credo Values

Innovation

Masters Complexity

Customer/ Marketplace Focus

Independent Partnering

 

Best Regards,

Komal Ahire

Sr. Talent Acquisition Specialist.

Ampcus Inc.

Employers have access to artificial intelligence language tools (“AI”) that help generate and enhance job descriptions and AI may have been used to create this description. The position description has been reviewed for accuracy and Dice believes it to correctly reflect the job opportunity.
  • Dice Id: 10115448
  • Position Id: 26-14639
  • Posted 1 day ago
Contact the job poster
SB

Sunil Baviskar

Recruiter @ Ampcus Inc
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