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Compliance Specialist II 1st Shift

Job

Adecco USA, Inc.

Northborough, MA (In Person)

$83,200 Salary, Full-Time

Posted 1 week ago (Updated 1 week ago) • Actively hiring

Expires 7/6/2026

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Job Description

Home Compliance Specialist II 1st Shift Healthcare & Life Sciences $ 34•$ 46 / Hour location_on Northborough, Massachusetts acute Contract/Temporary favorite_border
JOB ON CANDIDATE PORTAL
COPY LINK link 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 andpliance 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 adnce 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 andpliance excellence. Key Responsibilities GMP Compliance & Quality Operations Ensure all activities are conducted inpliance 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 timelypletion of quality checks Trend and analyze AQL failures in accordance with defined procedures and reporting requirements Support batch release activities ensuringpliance 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 adnce to quality standards on the shop floor Communicate quality findings, corrective actions, and performance metrics to relevant stakeholders Support quality walkthroughs andpliance 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 regulatorypliance 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 escalatepliance issues Excellentmunication skills for cross-functional collaboration Ability to work independently in a fast-paced, regulated manufacturing environment Core Competencies Strongmitment to quality and regulatorypliance 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 oues Strongmunication 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, andpliance 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,muter 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 w applicable. Equal Opportunity Employer/Veterans/Disabled Military connected talent encouraged to To read our Candidate Privacy Information Statement, which explains how we will use your information, please navigate to adecco/en-us/candidate-privacy The Company will consider qualified applicants with arrest and conviction records in accordance with federal, state, and local laws and/or security clearance requirements, including, as applicable: The California Fair Chance Act Los Angeles City Fair Chance Ordinance Los Angeles County Fair Chance Ordinance for Employers San Francisco Fair Chance Ordinance
Massachusetts Candidates Only:
It is unlawful in Massachusetts to require or administer a lie detector test as a condition of employment or continued employment. An employer who violates this law shall be subject to criminal penalties and civil liability.
Ref:
US_EN_99_101084_2552009