QC Analyst II (Microbiology) *PC 456

Your Tasks:

This position is primarily responsible for executing day-to-day activities under close supervision to support the micro programs (lentiviral vector and cell and gene therapy) in all stages of development in compliance with internal company policies and regulatory guidance (ICH, CFR, etc.).

Essential Duties and Responsibilities:

• Receive and track sample submissions from multiple departments.
• Sample and test samples aseptically per procedure.
• Maintain equipment and organization
• Identify out of trend or atypical results and supports ongoing investigations, initiate quality event investigations for deviations, OOT, and OOS events.
• Interact with functional peer groups; provide microbiological data to other departments upon request.
• Support and assist with documenting microbiological program metrics in support of management review.
• Ensure timely completion of microbial testing.
• Maintain trackers for microbial data.
• Initiate contract laboratory purchase orders for microbial testing; coordinate sample shipments to contract laboratories and/or sample storage vendors.
• Lab maintenance.

Requirements:

• Bachelor's (B.S.) in biotechnology, biology, chemistry or similar field from a four-year college or university; 2-4 years of experience working in a cGMP laboratory and performing hands on work in a Quality Assurance/Quality Control setting OR at least three years of experience working in a cGMP laboratory or field and performing hands on work in a Quality Assurance/Quality Control/Manufacturing/Materials Management setting; Or a combination of education and experience.
• The ideal candidate will have a basic knowledge of inventory and sample handling.
• Strong organizational skills and attention to detail are required.
• Excellent written and oral communication skills and must be able to interact with a cross-functional team members.
• Strong skills with Microsoft Office applications (Excel, Office, PowerPoint, Outlook, etc.)

Physical Demands:

The physical demands described here are representative of those that must be met by an employee to successfully perform the essential functions of this job. Reasonable accommodations may be made to enable individuals with disabilities to perform the essential functions. While performing the duties of this job, the employee is regularly required to walk; use hands to finger, handle, or feel; reach with hands and arms, talk, and hear. The employee is required to stand; climb or balance and stoop, kneel, crouch. The employee must occasionally lift and/or move up to 25 pounds. Specific vision abilities required by this job include close vision, color vision, peripheral vision, depth perception and ability to adjust focus. Must have ability to handle more than one task at a time and must work at a rapid pace while maintaining attention to detail.

Work Environment:

The work environment characteristics described here are representative of those an employee encounters while performing the essential functions of this job. This job is performed in a temperature-controlled facility without exposure to extreme hot or cold temperatures. Generally, this job is performed in a clean laboratory setting and routinely uses standard medical and research equipment such as centrifuges, biosafety cabinets, microscopes, incubators, pipettes and computers. While performing the duties of this job, the employee is exposed to viruses and bacteria. Employees entering the laboratory must wear appropriate clothing and protective equipment such as lab coats, glasses and gloves. The noise level in the work environment is usually moderate.

The anticipated base salary range has been established at $34.71-$46.97/hour. The hiring range for this position is expected to fall between $34.71-$37.77/hour, reflecting the range candidates can reasonably expect to be considered for at time of offer, based on factors such as experience, internal equity, and qualifications.

The salary of the finalist(s) selected for this role will be set based on a variety of considerations, including but not limited to internal equity, experience, education, specialization, skills, abilities, and training. The above range represents the Company's good faith and reasonable estimate of possible compensation at the time of posting.

In addition to your salary, the Company offers a comprehensive benefits package, including health, vision, and dental insurance, as well as a 401(k) plan. All benefits are subject to eligibility requirements. Certain positions may also be eligible for additional compensation such as bonuses or commissions.

Miltenyi Biotec, Inc is an EO Employer - M/F/Veteran/Disability/Sexual Orientation/Gender Identity

Miltenyi Biotec, Inc. participates in E-Verify.

Are you ready to start revolutionizing biomedical research? When you join Miltenyi Biotec, you join a family that is passionate about making a real impact - one breakthrough at a time. One integral division of that Miltenyi Biotec family is Miltenyi Bioindustry - our contract development and manufacturing organization (CDMO). As a full-scale CDMO, we provide customers with services for the development and manufacturing of lentiviral vectors and cell and gene therapy products. This crucial arm of our enterprise bridges the gap between research and mass bioproduction, ensuring that our solutions are accessible on a global scale. Miltenyi Bioindustry plays a unique role as both the producer and the service provider, relying on our instruments and reagents for each workflow step, controlling the entire supply chain and thus delivering greater security and planning clarity to our customers.