Quality Control Analyst

Posted Yesterday
Be an Early Applicant
Westborough, MA, USA
In-Office
70K-100K Annually
Mid level
Pharmaceutical
The Role
Perform microbiology QC testing and environmental monitoring in a cGMP cleanroom: collect EM samples, run bioburden, ID, growth promotion and endotoxin assays, review data, support instrument qualifications, author procedures, investigate deviations, and support manufacturing release and cleanroom qualifications.
Summary Generated by Built In
Job Summary & Responsibilities

Quality Control Analyst 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, 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 investigations 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.
Preferred Qualifications

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 weekend 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

 #LI-TR1

 

Skills Required

  • B.S. in Biology/Microbiology with 3+ years industry QC lab experience, or M.S. with 0-2 years
  • Demonstrated aseptic technique and common microbiological testing experience
  • Ability to gown into and work inside cleanrooms for environmental monitoring
  • Experience performing bioburden testing, microbial identification, growth promotion, and endotoxin analysis
  • Strong documentation, data organization, attention to detail, and willingness to learn
  • Adherence to lab safety standards and procedures
  • Ability to perform routine work independently with minimal instruction
  • Ability to work in a fast-paced team environment and complete assigned work timely
  • Strong interpersonal and collaboration skills within multidisciplinary teams
  • Prior QC experience and knowledge of cGMPs and regulatory requirements pertaining to biotechnology and pharmaceutical industry
  • Modeling company core values and promoting team culture and compliance

Astellas Pharma Compensation & Benefits Highlights

The following summarizes recurring compensation and benefits themes identified from responses generated by popular LLMs to common candidate questions about Astellas Pharma and has not been reviewed or approved by Astellas Pharma.

  • Retirement Support Retirement benefits include both a company match and an additional employer contribution, positioning the savings plan as notably generous. Complementary financial supports such as a dedicated wellness allowance reinforce long-term financial security.
  • Parental & Family Support Paid parental and family care leave, inclusive fertility and adoption assistance, and backup care resources signal a comprehensive, caregiver-friendly approach. Programs are framed to support diverse family-forming paths and ongoing caregiving needs.
  • Leave & Time Off Breadth A wide array of holidays, sick time, volunteer days, and extended disability income protection expands flexibility for time away. Immediate eligibility and broad coverage help employees access these supports without delay.

Astellas Pharma Insights

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The Company
HQ: Tokyo
5,446 Employees

What We Do

At Astellas, we strive to be a cutting-edge, value-driven life science innovator. This means working at the forefront of healthcare change to turn innovative science into the best outcomes for patients. Operating in approximately 70 countries with more than 14,000 employees, we are relentless in our pursuit of scientific progress and in tackling unmet medical needs. Visit our Global Astellas LinkedIn Community Guidelines to learn more about interacting with this page: https://www.astellas.com/en/global-linkedin-community-guidelines

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