Quality Technician

Bionostics, Inc.; Harvard (MA); On-site; USD 40,000 - 60,000; Full time

Benefits offered by this job

Medical, dental, vision insurance

401(k) plan

Tuition reimbursement

Paid time off and holidays

Employee events

Job summary

Bionostics, Inc. in Harvard, Massachusetts is seeking a Quality Technician who reports to the Quality Control Manager. The role involves in-process and final QC testing of products, conducting instrument validations, and routine lab maintenance.

The ideal candidate will possess a High School degree, at least 2 years of relevant technical experience, and be available for overtime and weekend work. Competitive benefits include insurance, 401(k), and educational opportunities.

Qualifications

• High School degree with 2+ years of relevant technical experience.
• Science or quality-related associate’s degree with 1+ year of experience.
• Availability for overtime and weekend work is required.

Responsibilities

• Responsible for in-process and final QC testing of products.
• Participates in instrument validations and routine lab maintenance.
• Documents results and compiles data reports.

Skills

Communication skills

Laboratory practices

Attention to detail

Time management

Education

High School degree with 2+ years relevant experience

Associate's degree in science or quality-related field

Bachelor's degree in science or quality-related field

Job description

Position Summary

Quality Technician reports to the Quality Control Manager and is responsible for in-process and final QC testing of Bionostics products. Quality Technicians also participate in instrument validations, routine lab maintenance activities, and help monitor and sustain laboratory and process inventories.

Principal Responsibilities

• Understands and adheres to all quality technician job requirements: participates in proficiency rotations through key areas of responsibility in the lab.
• Follows work instructions carefully and demonstrates good documentation practices.
• Documents results, processes testing, and refers to past batch records when needed.
• Compiles, analyzes, and reports on data conformity.
• Manages time well and puts in extended time as needed.
• Demonstrates flexibility to work on multiple tasks with increased effectiveness.
• Work may change from day-to-day within reasonable and expected boundaries.
• Demonstrates knowledge of work performed by the department and continues to learn how to perform multiple functions within the department.
• Works independently with minimal supervision on routine tasks.
• Demonstrates excellent oral and written communication skills.
• Follows priorities given by supervisor, completing other duties as assigned.
• Supports and helps others on the team, participates in training of new employees.
• Performs laboratory maintenance tasks.
• Performs daily qualifications and routine maintenance as needed.
• Understands and ensures proper function of equipment.
• Understands and follows good laboratory practices and site-specific lab protocols regarding:
• Chemical handling and hazards
• Labeling
• Safety procedures
• Department specific SOPs
• Proper use and maintenance of laboratory instrumentation
• Understands site applicable databases, including controlled documentation systems and data management software.
• Collaborates with other departments and team members to make modifications to controlled documentation through the current electronic record keeping system.
• Meets quality expectations.
• Understands importance of good manufacturing practices and adheres to good laboratory practices.
• Understands the basic ISO protocols and other applicable standards.
• Completes all compliance trainings as assigned.
• Participates in continuous process improvements efforts.
• Performs facility monitoring tasks including:
• Daily monitoring of temperature-controlled areas using calibrated devices. Reviews temperature monitoring records.
• Environmental monitoring and high purity water monitoring. Reviews environmental monitoring records.
• Monitors lab inventory and orders lab supplies as required.
• Reviews log books and orders consumables as required.
• Assists in instrument validations for new equipment and test method validations for new assays.

Qualifications

• High School degree with 2+ years of relevant technical experience.
• Science or quality-related associate’s degree with 1+ year of experience.
• Science or quality-related bachelor’s degree with a minimum of 0+ years of experience.
• Availability for overtime and weekend work is required.

Physical Requirements

• Lifting smaller boxes less than 20 lbs.
• Ability to work while standing at laboratory bench for long periods of time.
• Ability to focus on required work.

Benefits

• Competitive insurance benefits starting on day one: medical, dental, vision, life, short-term disability, long-term disability, pet, legal and ID shield.
• 401(k) plans, employee stock purchase plan (ESPP), HSA, FSA, and dependent care FSA.
• Mentorship, promotional opportunities, training and development, tuition reimbursement, internship programs.
• Employee resource groups, volunteer paid time off, employee events, and charity drives.
• Accrued leave policy with paid holidays, paid time off, and paid parental leave.

EEO Statement

Bio-Techne is an E-Verify Employer in the United States. All qualified applicants will receive consideration for employment without regard to race, color, religion, sex, sexual orientation, gender identity, national origin, disability, or status as a protected veteran. To protect the interests of all, Bio-Techne will not accept unsolicited resumes from any source other than a candidate application. Any unsolicited resumes sent to Bio-Techne will be considered Bio-Techne property.

If you require a reasonable accommodation to complete an application, participate in an interview, or take part in any other stage of the recruitment process, please contact [e-mail] for assistance.