Quality Control Analyst II Microbiology MA-TC

Astellas Pharma; Westborough (MA); On-site; USD 70,000 - 100,000; Full time

Benefits offered by this job

Medical, Dental and Vision Insurance

401(k) match and company contribution

Company paid life insurance

Annual Corporate Bonus and Quarterly 5

Long Term Incentive Plan

Company fleet vehicle for eligible

Referral bonus program

Job summary

Astellas Pharma is seeking a QC Analyst II in Microbiology to support the AIRM GMP Environmental Monitoring program. You will perform and review laboratory testing, develop technical documents, and contribute to training.

This on-site, day-shift role focuses on EM testing, bioburden analyses, and data trend reporting in a GMP environment. You will gown into cleanrooms, follow strict GMP practices, and coordinate with contract labs.

Qualifications

• B.S. in Biology or Microbiology with 3+ years or MS with 0-2 years of industry experience in QC.
• Aseptic techniques and common microbiological testing experience.
• Must gown into cleanrooms to perform EM testing.
• Strong documentation, data organization, and attention to detail.
• Adherence to lab safety standards and procedures.
• Ability to perform routine work independently with minimal instructions.
• Excels in a fast-paced team environment and collaborative work style.
• Day shift, Monday–Friday, with potential GMP operations support.

Responsibilities

• Attire gowning for Grade B/A manufacturing areas and collect EM samples.
• Perform QC testing of samples for bioburden, microbial ID, growth promotion, and Endotoxin analysis.
• Receive manufacturing samples for QC analysis and coordinate testing with contract labs.
• Review EM plates, lab data, logbooks, and documents for product release and trend reports.
• Follow aseptic practices and GMP/GLP guidelines in all tasks.
• Assist with assay/instrument qualification, troubleshooting, and procedure/report writing.
• Update laboratory procedures and contribute to EM data trend reports.
• Support cleanroom/gowning qualification and personnel monitoring.

Skills

Aseptic techniques

Microbiological testing

Gowning into cleanrooms

Documentation and data organization

Lab safety compliance

Independent work

Team collaboration

Day shift availability

Education

B.S. in Biology/Microbiology

MS in Microbiology

Job description

Quality Control Analyst II Microbiology MA-TC

About Astellas

Astellas is a global life sciences company committed to turning innovative science into VALUE for patients. We provide transformative therapies in disease areas that include oncology, ophthalmology, urology, immunology and women's health. Through our research and development programs, we are pioneering new healthcare solutions for diseases with high unmet medical need. Learn more at Astellas.com.

Are you driven to make a real difference in the lives of patients?
We're seeking passionate individuals who thrive in dynamic environments, embrace new ideas, and aren’t afraid to take intelligent risks. People who act with unwavering integrity and are deeply committed to making a tangible impact.

Purpose & Scope
QC Analyst II, Microbiology will provide support to the AIRM GMP Environmental Monitoring (EM) program and microbial testing. This role is responsible for performing and reviewing laboratory testing, developing and managing technical documents, and conducting training. This role is scheduled for Monday to Friday Day shift supporting GMP operations.

Role And Responsibilities

• Attire gowning for Grade B/A manufacturing areas and collect EM samples for viable air, non-viable particulates, and surface viable samples.
• Perform QC testing of samples for bioburden, microbial identification, growth promotion, and Endotoxin analysis.
• Receive manufacturing samples for QC analysis, ship samples to the contract labs testing, review data for lot disposition.
• Read and Review routine EM plates, lab testing data, logbooks, and documents for product release and trend reports.
• Understand and follow aseptic behavior, good laboratory and manufacturing practices, and documentation.
• Help with assay/instrument qualification, troubleshooting, and procedure/report writing.
• Author/update laboratory procedures, protocols, and help in EM data trend reports.
• Support cleanroom qualification, gowning qualification, aseptic process qualification, and personnel monitoring for manufacturing activities.
• Initiate Incident reports for OOS results and work with the team to find a root cause and corrective actions.
• Perform QC lab support activities like lab set up, housekeeping, instrumentation maintenance, and coordinate instrument calibration.

Required Qualifications

• B.S. degree in Biology/Microbiology with 3+ years or MS with 0-2 years of relevant industry experience in a QC lab.
• Demonstrated experience of aseptic techniques and common microbiological testing.
• Must be able to gown into cleanrooms to perform EM testing.
• Good documentation, data organization, detail oriented, and willingness to learn.
• Must be capable of observing and adhering to lab safety standards and procedures.
• Successfully performs routine work independently with minimal instructions.
• Excels in a fast-paced team environment and completes assigned work in timely fashion.
• Strong interpersonal skills, highly collaborative within a multi-disciplinary team and contributes to a supportive and positive work environment.
• This role is scheduled to work during Day shift on Monday to Friday and flexibility may be required to support GMP Operations.

Preferred Qualifications

• Prior experience in QC environment, knowledge of cGMPs and regulatory requirements pertaining to biotechnology and pharmaceutical industry.
• Model our core values- Be Bold, Care Deeply, getting stuff done- while promoting the team culture and Compliance.

Location and Working Environment

• This role frequently requires long hours of sitting, standing and use of hands and regular motion to include bending, stooping, and lifting to 35lbs.
• Requires gowning inside the cleanroom for extended periods of time.
• Use of gloves and mask is required to prevent exposure to biohazards and viruses.
• This is an on-site role working in a cGMP regulated manufacturing facility.

What awaits you at Astellas?

• Global collaboration: Become part of a connected global business of like-minded life science leaders, all dedicated to improving patients' lives worldwide.
• Real-world patient impact: Contribute to transformative therapies that reach patients around the world, knowing your work makes a difference every day.
• Relentless Innovation: Join a company at the forefront of scientific breakthroughs, where you'll have the opportunity to shape the future of healthcare.
• A Culture of Growth: Chart your own course within a supportive environment that values your contributions, champions your development, and empowers you to pursue your passions.

Our Organizational Values and Behaviors
Values: Innovation, Integrity and Impact sit at the heart of what we do. Behaviors: We come together as ‘One Astellas’, working with courage and a sense of urgency. We are outcome focused and consistently take accountability for our personal contribution.

Salary Range
$69,790-99,700 (Final compensation will be determined based on a variety of factors, including but not limited to skills, experience and organizational equity considerations)

Benefits

• Medical, Dental and Vision Insurance
• Generous Paid Time Off options, including Vacation and Sick time, plus national holidays including year-end shut down
• 401(k) match and annual company contribution
• Company paid life insurance
• Annual Corporate Bonus and Quarterly Sales Incentive for eligible positions
• Long Term Incentive Plan for eligible positions
• Company fleet vehicle for eligible positions
• Referral bonus program

Category Massachusetts TC
Astellas is committed to equality of opportunity in all aspects of employment. EOE including Disability/Protected Veterans