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Compliance Specialist II 1st Shift

Job in Northborough, Worcester County, Massachusetts, 01532, USA
Listing for: Adecco US, Inc.
Full Time position
Listed on 2026-06-04
Job specializations:
  • Quality Assurance - QA/QC
    Quality Control / Manager, Quality Technician/ Inspector, QA Specialist / Manager, Data Analyst
Salary/Wage Range or Industry Benchmark: 34 - 46 USD Hourly USD 34.00 46.00 HOUR
Job Description & How to Apply Below
** Adecco Healthcare & Life Sciences*
* ** Research Associate II - Quality & GMP Compliance*
* ** Fully Onsite | Full-Time*
* Pay: 35- 46/hr DOE

** Position Summary*
* The Research Associate II is responsible for supporting quality assurance and compliance activities within a GMP-regulated manufacturing and laboratory environment. This role focuses on finished product inspection, retention sample management, quality systems support, and cross-functional collaboration with production and quality teams to ensure adherence to regulatory and internal standards.

The position plays a key role in maintaining product quality throughout the lifecycle, supporting audits and inspections, and driving continuous improvement and compliance excellence.

** Key Responsibilities*
* ** GMP Compliance & Quality Operations*
* + Ensure all activities are conducted in compliance with GMP and applicable regulatory requirements

+ Perform finished product inspections according to established standards, specifications, and timelines

+ Conduct AQL (Acceptable Quality Limit) inspections and ensure timely completion of quality checks

+ Trend and analyze AQL failures in accordance with defined procedures and reporting requirements

+ Support batch release activities ensuring compliance with GMP guidelines

** Sample & Retention Material Management*
* + Manage sampling, storage, monitoring, and maintenance of finished product retention samples

+ Perform annual inspections of retention samples according to defined procedures

+ Ensure proper documentation and traceability of all retention sample activities

** Quality Systems & Documentation*
* + Support creation, revision, and periodic review of product and material specifications

+ Perform document control activities including creation, revision, and archival of quality documentation

+ Support Quality Management System processes including Change Control, Deviations, and CAPA investigations

** Investigation & Continuous Improvement*
* + Support root cause analysis investigations for quality incidents and assist in implementing corrective and preventive actions (CAPA)

+ Identify discrepancies and escalate quality-related issues in a timely manner

+ Support risk management initiatives to prevent recurrence of quality issues

+ Contribute to continuous improvement initiatives and quality performance enhancements

** Audit & Cross-Functional Support*
* + Participate in internal and external audits and regulatory inspections

+ Provide documentation and subject matter support during inspections

+ Collaborate closely with production teams to ensure adherence to quality standards on the shop floor

+ Communicate quality findings, corrective actions, and performance metrics to relevant stakeholders

+ Support quality walkthroughs and compliance reviews

** Required Qualifications*
* + Bachelor's degree required

+ Minimum of 3 years of experience in quality assurance, GMP manufacturing, laboratory operations, or regulated industry environment

+ Strong understanding of GMP principles and regulatory compliance requirements

+

Experience with quality systems such as Change Control, CAPA, and Deviations

+ Ability to perform structured inspections, documentation, and trend analysis

+ Strong attention to detail and ability to identify and escalate compliance issues

+ Excellent communication skills for cross-functional collaboration

+ Ability to work independently in a fast-paced, regulated manufacturing environment

** Core Competencies*
* + Strong commitment to quality and regulatory compliance

+ Analytical thinking and problem-solving ability

+ High attention to detail and documentation accuracy

+ Proactive escalation and risk identification mindset

+ Ability to work in cross-functional production and quality environments

+ Continuous improvement mindset and accountability for outcomes

+ Strong communication and stakeholder coordination skills

** Work Environment*
* + Fully onsite role within GMP-regulated manufacturing/quality environment

+ Frequent interaction with production floor and quality systems

+ Active participation in inspections, audits, and compliance reviews

** Pay Details:**  $34.00 to $46.00 per hour

Benefit offerings available for our associates include medical, dental, vision, life insurance, short-term disability, additional voluntary benefits, EAP program, commuter benefits and a 401K plan. Our benefit offerings provide employees the flexibility to choose the type of coverage that meets their individual needs.  In addition, our associates may be eligible for paid leave including Paid Sick Leave or any other paid leave required by Federal, State, or local law, as well as Holiday pay where applicable.

Equal Opportunity Employer/Veterans/Disabled

Military connected talent encouraged to apply

To read our Candidate Privacy Information Statement, which explains how we will use your information, please navigate to

The Company will consider qualified applicants with arrest and conviction records in accordance with federal, state, and local laws and/or…
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