Description

The Quality Control Analyst II will be responsible for conducting routine and complex testing of in-process samples and final products in alignment with Standard Operating Procedures (SOPs) and relevant procedures. This includes method development, qualification, validation, method transfer, product release, stability, and process validation and investigations.

Company Culture and Environment
The workplace emphasizes compliance with CGMPs (Current Good Manufacturing Practices) and fosters a culture of safety, teamwork, and continuous improvement. Employees are encouraged to engage in problem-solving and suggest process enhancements which highlights an environment that values input from all team members.

Career Growth and Development Opportunities
This position offers exposure to various testing methodologies and collaborative problem-solving, providing opportunities for professional development and potential advancement within the quality control field.

Detailed Benefits and Perks
While specific benefits are not explicitly mentioned, working in the pharmaceutical sector typically includes competitive pay rates and a focus on career advancement.

Compensation and Benefits

• Competitive pay rate of $35.00/hr on W2
  
• Opportunity for contract duration of 12 months with potential for extension
  
• Onsite work environment
  
• Experience in a reputable pharmaceutical client

Why you should apply for this position today
This role presents a unique opportunity to make a significant impact within a leading pharmaceutical company, gaining valuable experience in quality control that is crucial for career advancement.

Skills

• Basic knowledge in required method platforms (e.g., Bioburden, TOC, Endotoxin, Water Chemistry, ELISA)
• Attention to detail with excellent record-keeping and proofreading skills
• Effective communication skills
• Ability to work both independently and as part of a team
• Proficiency in Microsoft Office tools such as Word, Excel, and PowerPoint

Responsibilities

• Perform laboratory assays supporting method development, qualification, validation, and investigations
  
• Conduct maintenance on complex laboratory equipment
  
• Review data to ensure compliance with procedures and specifications
  
• Calculate and evaluate results
• Document detailed observations for Alert, Action, and OOS result investigations
  
• Assist in writing and revising SOPs
  
• Participate in the qualification of new controls, standards, and reagents
  
• Adhere to safety procedures and guidelines
• Actively engage in problem-solving meetings and suggest process improvements
  
• Work independently under supervision and direction

Qualifications

• Bachelor’s degree or equivalent with 2+ years of laboratory experience
  
• Master’s degree or equivalent with 0-1 year of experience
  
• Basic knowledge (1-2 years of experience) in required method platforms

Education Requirements

• Bachelor’s degree in a relevant scientific field or equivalent experience
  
• Master’s degree preferred but not required

Education Requirements Credential Category

• Bachelor’s or Master’s degree in a related scientific discipline
  

Experience Requirements

• 2+ years of laboratory experience for Bachelor’s degree holders
  
• 0-1 year of experience for Master’s degree holders
  
• Experience with relevant method platforms (e.g., Bioburden, TOC, Endotoxin)
  

Why work in Framingham, MA
Framingham, MA is a thriving town with a rich history and a strong sense of community. Known for its access to educational institutions and a variety of recreational activities, Framingham offers a vibrant lifestyle for professionals. The town’s proximity to Boston provides ample opportunities for networking and career advancement within the pharmaceutical sector.