Quality Assurance Specialist job in Cambridge, USA

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Last Name*

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Job type: Contract

Discipline: Good Manufacturing Practice (GMP), Good Clinical Practice (GCP), Good Laboratory Practice (GLP)

Location: United States

This vacancy has now expired. Please see similar roles below...

Quality Assurance Specialist - Contract - Onsite

Proclinical Staffing is seeking a Quality Assurance Specialist to join a global biopharmaceutical company. This is a contract role located in Cambridge, MA.

Primary Responsibilities

In this role, you will be responsible for overseeing the quality assurance process, ensuring that our products meet both Local and Global quality standards.

Skills & Requirements:

HS Diploma or equivalent and 8+ years of experience in a cGMP environment, OR associate degree and 6+ years of experience in a cGMP environment, OR bachelor's degree and 4+ years of experience in a cGMP environment.
Previous experience working with quality systems having oversight of cGMP production operations including some or all of the following: batch release, SAP, batch record review
Bachelor of Science or Bachelor of Arts degree in a scientific discipline.
Demonstrated experience in regulatory inspection activities.
Ability to work on multiple projects on a tight timeline.
Ability to prioritize and the flexibility to adapt to changing priorities.
Working knowledge of cGMPs and associated regulatory requirements for the manufacture, testing, and release of pharmaceutical/biopharmaceutical products for international markets.
SAP knowledge
Experience working successfully both independently and in a team environment.
Strong verbal and written communication skills.
Able to interact with peers, subordinate and senior personnel in multidisciplinary environment including engineering, facility operations, validation, production, and QC.
Able to prioritize and decide appropriate course of actions.
Root cause analysis experience preferred.
Vaccines experience a plus.

The Quality Assurance Specialist will:

Execute all activities following quality and regulatory standards and procedures.
Promote a quality mindset and quality excellence approach to all activities.
Continue support of continuous improvement culture and industrial excellence methodologies.
Support employees and respective departments in a manner which is clear in approach, communication, and action.
Provide proactive communication to customers to ensure timely escalation and resolution of issues. Follow up on issues to ensure completion in a timely manner. Support cross functional communication in all manners.
Support batch release of drug substance including compilation of documentation
Perform review of the manufacturing batch records for completeness and compliance with cGMPs as per regulatory requirements and internal procedures.
Provide on the floor support to Manufacturing
Support SAP integration and master data migration for batch release activities
Working knowledge and/or ownership of the following quality systems: Change Control, CAPAs, Deviations, and Self inspection auditing, QA reporting and approval of GMP documentation.
Support GMP compliance and inspection readiness within organization. Assist in coordination of work for the QA Operations team to facilitate timely release of product lots.

If you are having difficulty in applying or if you have any questions, please contact Jackie Cerchio at (+1) 267-846-2026 or j.cerchio@proclinical.com.

Proclinical is a specialist employment agency and recruitment business, providing job opportunities within major pharmaceutical, biopharmaceutical, biotechnology and medical device companies.

Proclinical Staffing is an equal opportunity employer.

INDCQA