Compliance Specialist

Randstad USA; Ridgefield (NJ); On-site; USD 28,000 - 34,000; Full time

Benefits offered by this job

Medical insurance

Prescription coverage

Dental insurance

Vision insurance

AD&D

Life insurance

Short-term disability

401K plan

Job summary

Randstad USA in Ridgefield, NJ seeks a Compliance Specialist contract role to drive non-conformance investigations and safeguard quality standards in high-impact manufacturing operations. The position focuses on authorsing NCRs/deviations, CAPA processes, and ensuring regulatory compliance under GMP/ISO 9001 and FDA guidelines.

The candidate should have 2+ years in QA or manufacturing with a Bachelor's degree (or equivalent experience) and be local to the area for overtime/weekend needs.

Qualifications

• 2+ years of hands-on experience authoring, investigating, and managing NCRs and deviations in a cGMP manufacturing environment.
• Working knowledge of CAPA management, effectiveness checks, and document control systems.
• Strong familiarity with regulatory standards including cGMP, ISO 9001, and FDA guidelines.
• Local to Ridgefield, NJ (within a 45-minute commute) to support potential overtime and weekend needs.

Responsibilities

• 2+ years of direct, hands-on experience authoring and investigating NCRs/deviations
• 2+ years in manufacturing or Quality Assurance within regulated environments (GMP, ISO 9001, FDA guidelines).
• High School Diploma/GED with 8-10 years' experience, or Bachelor's Degree with 3-5 years' experience.
• Proficiency with Microsoft Office Suite (Word, Excel).

Skills

GMP

CAPA

Root cause analysis

Education

Bachelor's

Job description

job summary: Are you an expert Quality Specialist driven by precision and root-cause problem-solving? A top-tier global pharmaceutical leader in Ridgefield, NJ, is seeking a dedicated Compliance Specialist to drive non-conformance investigations and safeguard quality standards in high-impact manufacturing operations.

location: Ridgefield, New Jersey

job type: Contract

salary: $20 - 25 per hour

work hours: 9 to 5

education: Bachelors

Responsibilities:

• 2+ years of direct, hands-on experience authoring and investigating NCRs/deviations
• 2+ years in manufacturing or Quality Assurance within regulated environments (GMP, ISO 9001, FDA guidelines).
• High School Diploma/GED with 8-10 years' experience, or Bachelor's Degree with 3-5 years' experience.
• Proficiency with Microsoft Office Suite (Word, Excel).

#LI-MH1

Qualifications:

• 2+ years of hands-on experience authoring, investigating, and managing NCRs and deviations in a cGMP manufacturing environment.
• Working knowledge of CAPA management, effectiveness checks, and document control systems.
• Strong familiarity with regulatory standards including cGMP, ISO 9001, and FDA guidelines.
• Proven tenure and stability in previous quality assurance or manufacturing roles.
• Local to Ridgefield, NJ (within a 45-minute commute) to support potential overtime and weekend needs.

#LI-MH1

skills: Good Manufacturing Practices (GMP), Corrective and Preventive Actions (CAPA)

Equal Opportunity Employer: Race, Color, Religion, Sex, Sexual Orientation, Gender Identity, National Origin, Age, Genetic Information, Disability, Protected Veteran Status, or any other legally protected group status.

At Randstad, we welcome people of all abilities and want to ensure that our hiring and interview process meets the needs of all applicants. If you require a reasonable accommodation to make your application or interview experience a great one, please contact [e-mail].

Pay offered to a successful candidate will be based on several factors including the candidate's education, work experience, work location, specific job duties, certifications, etc. In addition, Randstad offers a comprehensive benefits package, including: medical, prescription, dental, vision, AD&D, and life insurance offerings, short-term disability, and a 401K plan (all benefits are based on eligibility).

This posting is open for thirty (30) days.

• 2+ years of hands-on experience authoring, investigating, and managing NCRs and deviations in a cGMP manufacturing environment.

• Working knowledge of CAPA management, effectiveness checks, and document control systems.

• Strong familiarity with regulatory standards including cGMP, ISO 9001, and FDA guidelines.

• Proven tenure and stability in previous quality assurance or manufacturing roles.

• Local to Ridgefield, NJ (within a 45-minute commute) to support potential overtime and weekend needs.

#LI-MH1