Massachusetts Jobs

Great opportunity to get your foot in the door with one of the top Biotech companies in the Worcester, MA area!

If interested, please reach out directly to Lindsee Allienello at lallienello @ actalentservices.com

Description:

The Quality Associate supports the Quality Function that they are responsible for within Operations. This could include: Incoming Quality Assurance of drugs and packaging materials Manufacturing Quality Assurance Validation Quality Engineering Training and Regulatory Compliance. Expectations that the Quality Associate will maintain high quality levels on all aspects of their job while achieving high levels of efficiency.

Responsibilities :

• Responsible for various aspects of quality assurance and quality control related to their functional area.

• Ensures that product within the plant is consistently manufactured in conformance with company Quality System requirements and all applicable regulatory requirements.

• Support troubleshooting and resolution of quality compliance issues.

• Communicates with Management for Quality Management Review Quality Initiatives etc.

• Incumbent is responsible for quality decisions related to their functional area to ensure compliance with company Quality Systems and cGMPs.

  Qualifications :

• Must be familiar with use of electronic document management and laboratory information management.

• Must also be familiar with Quality Systems as well as cGMP and other regulatory requirements.

• Strong communication skills both oral and written

Years of experience/education and/or certifications required:

• Bachelors Degree/ 2 years of combined experience in Manufacturing QA QC RD in pharmaceutical or biologics industry

Top 3-5 skills requirements should this person have?

• Whether it is through manufacturing or quality control a certain level of quality experience is necessary.

• some form of review experience: data or record review

• 1 years within a manufacturing facility

• Bonus: some work with investigations

• Bonus: experience with document revisions

• Bonus: review of GMP commercial batch records

Experience Level:

Entry Level

About Actalent

Actalent is a global leader in engineering and sciences services and talent solutions. We help visionary companies advance their engineering and science initiatives through access to specialized experts who drive scale, innovation and speed to market. With a network of almost 30,000 consultants and more than 4,500 clients across the U.S., Canada, Asia and Europe, Actalent serves many of the Fortune 500.

Diversity, Equity & Inclusion

At Actalent, diversity and inclusion are a bridge towards the equity and success of our people. DE&I are embedded into our culture through:

• Hiring diverse talent

• Maintaining an inclusive environment through persistent self-reflection

• Building a culture of care, engagement, and recognition with clear outcomes

• Ensuring growth opportunities for our people

The company is an equal opportunity employer and will consider all applications without regard to race, sex, age, color, religion, national origin, veteran status, disability, sexual orientation, gender identity, genetic information or any characteristic protected by law.

If you would like to request a reasonable accommodation, such as the modification or adjustment of the job application process or interviewing process due to a disability, please email actalentaccommodation@actalentservices.com (%20actalentaccommodation@actalentservices.com) for other accommodation options.