Biotechnician I

3M HEALTHCARE; Hopewell (VA); On-site; USD 34,440 - 45,460; Full time

Benefits offered by this job

Medical, dental, vision

401(k)

FSA/HSA

Life insurance

Paid time off

Wellness programs

Job summary

BeOne is seeking an experienced Biotechnician I to join a GMP manufacturing environment in a cleanroom setting. You will participate in all phases of drug product formulation, filling, lyophilization, labeling, and packaging under ISO requirements.

Responsibilities include equipment setup, transfer operations, and maintaining proper documentation while adhering to cGMP batch records and SOPs.

Qualifications

• Aseptic gowning experience in cleanrooms.
• Strong time-management and organizational skills.
• Ability to work under pressure and meet tight timelines.

Responsibilities

• Start-up, troubleshooting, and acceptance testing of equipment.
• Perform floor operations during clinical and GMP campaigns.
• cGMP manufacturing equipment cleaning and sterilization.
• Solution preparation and transfer.
• Room and equipment cleaning.
• Equipment and process troubleshooting.
• Operate autoclaves and parts washers.
• Good documentation practices.
• Environmental monitoring.
• Report hazards or injuries promptly.

Skills

Aseptic gowning

Time management

Work under pressure

Team player

Prioritization

Attention to detail

Flexibility to shift

Punctuality

Fast-paced adaptation

Tools

Microsoft Office

Job description

General Description

BeOne continues to grow at a rapid pace with challenging and exciting opportunities for experienced professionals. When considering candidates, we look for scientific and business professionals who are highly motivated, collaborative, and most importantly, share our passionate interest in fighting cancer.

Required Skills & Attributes

• Demonstrated ability to successfully gown into aseptic manufacturing areas.
• Excellent organization and time‑management skills.
• Ability to manage heavy workload and aggressive timelines, prioritize and work under pressure.
• Strong work ethic, positive attitude, problem solving, team player, self‑confidence, and ability to accept and apply lessons learned as needed.
• Works with a sense of urgency while engaging and listening to experts.
• Ability to work in a fast‑paced environment demonstrating excellent time‑management and organizational skills.
• Strong organizational skills with proven ability to prioritize.
• Dependable and punctual.
• Proficient with standard Microsoft Office (Excel, Outlook, Word).
• Flexible to work 1st or 2nd shift with holidays, weekends, overtime as per business needs.

Responsibilities

• Equipment start‑up, troubleshooting, and acceptance testing.
• Execute floor operations during clinical and GMP campaigns.
• cGMP manufacturing equipment cleaning and sterilization.
• Solution preparation and transfer.
• Room and equipment cleaning.
• Equipment and process troubleshooting.
• Perform sterile filtration / integrity testing.
• Good documentation practices.
• Environmental monitoring.
• Operate autoclaves and parts washers.
• Set up DP equipment.
• Report any accidents, incidents, injuries, or illnesses immediately and notify manager of hazards, unsafe acts or conditions.
• Work hands‑on under ISO7, ISO8, ISO5 area and CNC, with a variety of manufacturing production equipment and technologies under direction of Production Supervisor.

Physical Requirements

• Stand for long periods (8–12 hours/day).
• Reach above shoulder level, bend/stoop, push/pull, handle/grip frequently.
• Work scheduled 40 hours with ability to work overtime.
• Comfortable with varying temperatures.
• Frequent lifting, pushing, pulling, carrying; ability to lift up to 40 lbs.
• Regular reaching, bending, stooping, twisting.
• Repetitive motion and substantial movement of wrists, hands, fingers.
• Environment requires dedicated gowns based on area.
• Work with hazardous materials and chemicals.
• Willing to work any shift and flexible to support business needs.

Essential Functions of the Job

The Biotechnician I positions operate in a cleanroom environment, following cGMP batch records and SOPs to manufacture drug products. Supports projects with GMP manufacturing personnel, prepares suites for manufacturing operation, and operates in a safe and compliant manner. Primary responsibility is to participate in all phases of drug product formulation, filling, lyophilization, visual inspection, labeling, and packaging, including requesting materials, set‑up, preparation, final filtration, formulation, filling vials inside a Grade A isolator with an automated filling machine, and subsequent labeling, visual inspection, and packaging.

Computer Skills

Strong PC literacy required; MS Office skills (Outlook, Word, Excel, PowerPoint).

Travel

International and domestic – periodically.

Global Competencies

• Fosters Teamwork
• Provides and solicits honest and actionable feedback
• Self‑Awareness
• Acts inclusively
• Demonstrates initiative
• Entrepreneurial mindset
• Continuous learning
• Embraces change
• Results‑oriented
• Analytical thinking / data analysis
• Financial excellence
• Communicates with clarity

Salary Range

$25.48 – $33.48 per hour.

Benefits

• Medical, dental, vision
• 401(k)
• FSA/HSA
• Life insurance
• Paid time off
• Wellness programs

EEO Statement

BeOne is proud to be an equal opportunity employer. BeOne does not discriminate on the basis of race, religion, color, sex, gender identity, sexual orientation, age, disability, national origin, veteran status or any other basis covered by applicable law. All employment is decided on the basis of qualifications, merit, and business need. Reasonable accommodations may be requested at [e-mail].