QC Scientist II, Microbiology

Do you want to be part of an inclusive team that works to develop innovative therapies for patients? Every day, we are driven to develop and deliver innovative and effective new medicines to patients and physicians.  If you want to be part of this exciting work, you belong at Astellas!

Astellas Pharma Inc. is a pharmaceutical company conducting business in more than 70 countries around the world. We are committed to turning innovative science into medical solutions that bring value and hope to patients and their families. Keeping our focus on addressing unmet medical needs and conducting our business with ethics and integrity enables us to improve the health of people throughout the world. For more information on Astellas, please visit our website at www.astellas.com.

The Role

The Scientist II QC Microbiology serves as senior technical subject matter expert responsible for overseeing microbiological testing programs supporting GMP operations. This role provides technical leadership across QC Microbiology and Manufacturing by ensuring effective microbiological testing, mentoring laboratory staff, supporting quality systems and delivering aseptic technique training to maintain compliance with GMP and contamination control requirements.

Responsibilities:

• Serve as subject matter expert for microbiological testing programs including environmental monitoring, sterility, endotoxin, mycoplasma, microbial identification, and contamination control.
• Support QC Microbiology Senior Manager in oversight of laboratory operations, technical initiatives, and microbiological program execution.
• Develop and deliver aseptic technique and contamination control training for manufacturing and QC personnel to maintain compliance with GMP and cleanroom practices.
• Track and support quality system activities including deviations, investigations, CAPAs, Change Control and trending associated with QC microbiology operations.
• Review and approve microbiological data, protocols, quarterly reports , SOPs and other technical documentation.
• Lead data trending and interpretation of environmental monitoring and microbiological data to identify risks and support contamination control strategy.
• Provide technical leadership and mentorship to microbiologists and junior scientist within QC microbiology laboratory.
• Author and review SOPs, protocols, validation reports, investigation reports and technical documents in accordance with GMP requirements.
• Lead or support method qualification, validation, and technology implementation for microbiological assays.
• Collaborate cross-functionally with Manufacturing, QA , Facilities and other teams to support manufacturing operations and process improvements.
• Support regulatory inspections, audits and responses by providing technical justification and documentation.

Qualifications:

Required Qualifications

• BS degree in Biology/Microbiology with 10 years or M.S. with 6 years of relevant experience in a GMP QC microbiology laboratory.
• Demonstrated advanced expertise in microbiological testing including environmental monitoring, bioburden, endotoxin, sterility, mycoplasma and microbial identification.
• Experience supporting aseptic manufacturing environments and cleanroom operations.
• Demonstrated experience mentoring laboratory staff and providing technical training.
• Strong knowledge of cGMP regulations and microbiological control strategies.
• Excellent technical writing and communication skills.
• 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 (8 am to 5 pm) Monday to Friday.
• Flexibility to work occasional weekend hours may be required to support GMP Operations.

 Preferred:

• Experience supporting Contamination Control Strategy (CCS) development and Annex I expectations.
• Experience leading aseptic training programs.
• Demonstrated leadership on cross-functional projects and operational improvements.

Working Environment:

• This position is based at 9 Technology drive, Westborough, MA and requires on-site work.
• This role involves both hands-on laboratory work and technical oversight activities including data review, investigation support and training of laboratory personnel.

Salary Range: $103,600 - $148,000 (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-paid fleet vehicle for eligible positions
• Referral bonus program

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Salary : $103,600 - $148,000