Quality Assurance Specialist jobs in Worcester, MA

Quality Assurance Specialist

$27 - $30 per hour with option for medical benefits.

6 month initial contract

Worcester, MA

Standard first shift

Orion Group and a market leading pharmaceutical company are seeking Quality Assurance Specialists in Worcester ASAP!!! Our client is in need of Quality Specialists to work within their Bioresearch Center!

We are seeking candidates with 2 years of combined experience in Manufacturing, QA, QC, R&D in pharmaceutical or biologics industry. Apply today and take the first step towards this amazing contract opportunity!!

Job Description:

The Quality Assurance Specialist 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 Assurance Specialist will maintain high quality levels on all aspects of their job while achieving high levels of efficiency.

Quality Assurance Specialist Daily 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 cGMP.

Qualifications for the Quality Assurance Specialist:

• 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
• Bachelor’s Degree/ 2 years of combined experience in Manufacturing, QA, QC, R&D in pharmaceutical or biologics industry

What are the 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

Job Types: Contract, Temporary

Benefits:

• 401(k)
• Dental insurance
• Health insurance
• Life insurance
• Vision insurance

Experience level:

• 2 years

Schedule:

• 8 hour shift
• Monday to Friday

Work setting:

• In-person
• Manufacturing facility
• Office

Education:

• Bachelor's (Required)

Experience:

• prior Quality Assurance: 2 years (Required)
• electronic document management and LIMS: 1 year (Required)
• CGMP requirements: 2 years (Required)
• Manufacturing, QA, QC, R&D in pharma/biologics industry: 2 years (Required)
• Veeva Vault: 1 year (Preferred)

Ability to Relocate:

• Worcester, MA 01605: Relocate before starting work (Required)

Work Location: In person