Senior QC Microbiology Technician — GMP Lab Pro

Regulatory Jobs; Massachusetts; On-site; USD 31,000 - 47,000; Full time

Benefits offered by this job

Medical benefits

Paid Time Off

Employee Referral Bonus

Career Advancement Opportunities

Job summary

Thermo Fisher Scientific is seeking a Senior Quality Control Technician in Massachusetts. You will perform microbial testing, environmental monitoring, and aseptic procedures to support GMP production and release testing for clinical and commercial biopharmaceuticals.

The role emphasizes method transfer, validation, data integrity, and adherence to GMP. You will operate in a lab setting with cleanroom protocols and be eligible for a variable bonus according to company policy.

Qualifications

• Minimum 0–2 years of work experience in a cGMP field.
• Bachelor’s degree in Microbiology or Biology preferred.
• Prolonged cleanroom work with PPE; ability to lift up to 40 lbs.

Responsibilities

• Perform microbial testing and environmental monitoring to support GMP production.
• Set up equipment and execute routine testing and documentation.
• Transfer and qualification of analytical methods; provide training as needed.
• Ensure GMP compliance and data integrity in all activities.

Skills

Microbiological testing

Environmental monitoring

Aseptic techniques

GMP regulations

Documentation practices

Quality standards

Attention to detail

Data integrity

Problem-solving

Microsoft Office

Laboratory information systems

Written & verbal communication

Independent & collaborative work

Physical dexterity

Cleanroom PPE compliance

Shift flexibility

Pharmaceutical/regulatory experience

Education

High School Diploma with GMP experience

Bachelor’s degree in Microbiology or Biology

Job description

Thermo Fisher Scientific is seeking a Senior Quality Control Technician in Massachusetts. You will perform microbial testing, environmental monitoring, and aseptic procedures to support GMP production and release testing for clinical and commercial biopharmaceuticals.

The role emphasizes method transfer, validation, data integrity, and adherence to GMP. You will operate in a lab setting with cleanroom protocols and be eligible for a variable bonus according to company policy.