Job Summary

This position is responsible for different stages of manufacturing of various BioLegend's regulated product produced in our US FDA registered cGMP manufacturing facility.

The candidate will be responsible for formulating, filling, capping, labeling, completing batch records, putting away finished good inventory (FGI), data entry, equipment maintenance and supply inspections & storage.

Other responsibilities include purification of monoclonal antibodies derived from tissue culture material through an AKTA system. As well as the conjugation of purified antibody through the AKTA system. Buffer preparation and inspection of incoming buffers into the GMP suite will also be performed.

Another part of the job responsibility includes preparing product/project related documentation and maintaining the device history records for all the regulated products. Working closely with product development on new products in order to establish a smooth transition into manufacturing will also be required.

The desired candidate must be a team-player who is organized and has strong verbal and written communication skills and is able to work in a very fast paced environment. Great attention to detail is also a skill that will allow the candidate to be successful. The candidate must also be able to work independently and meet deadlines.

Essential Functions

Reasonable accommodations may be made to enable individuals with disabilities to perform the essential functions.

• Prepare various buffers for manufacturing activities.
• Perform incoming inspection of raw materials.
• Perform formulation and vialing of the regulated products.
• Assist in troubleshooting the manufacturing process.
• Maintain batch records and other documentations that are essential to be in compliance with ISO13485:2016 and cGMP.
• Maintain/troubleshoot laboratory equipment and manage supplies.
• Process purification or conjugation orders as needed through the AKTA system.
• Perform dialysis, centrifugation, and column chromatography.
• Conduct Endotoxin tests.
• Advance multiple projects simultaneously and work in a team environment.
• Other projects or responsibilities as may be required.

iACT Competencies

• innovate - Be better, keep improving, be more efficient, creative, and be in the forefront of development
• Aspire - Have desire, purpose, and ambition challenging ourselves to push the limits and reach new heights
• Collaborate - Foster teamwork, common goals, selflessness, communication and mutual support
• Transform - Adapt, learn, re-invent and change for future development and growth

Minimum Qualifications - Education and Experience

• Bachelor's degree in life science with 2-3 years of relevant industry experience.
• Six months experience in a GMP environment
• One-year experience of antibody and recombinant protein purification/conjugation.

Preferred Qualifications - Education and Experience

• Bachelor's degree in life science with 3 years GMP lab experience in antibody and recombinant protein purification and conjugation.
• Extensive knowledge in ERP system such as Microsoft NAV

The base salary range for this full-time position is$65,000 - 67,000.This range reflects the minimum and maximum target for a new hire in this position. The base pay actually offered to the successful candidate will take into account internal equity, work location, and additional factors, including job-related skills, experience, and relevant education or training. Your recruiter can share more about the specific salary range for your preferred location during the hiring process.

Please note that base pay is only one part of our total compensation package and is determined within a range. This range allows for the successful candidate to have an opportunity to progress within the position and develop at our company. This base pay range does not take into account bonuses, equity, or other benefits which may be applicable and are dependent on the level and position offered.

Work Environment & Physical Demands

Lab

While performing the duties of this job, the employee regularly works in a laboratory environment with occasional data entry on a computer. Occasional exposure to a warehouse environment.

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.

While performing the duties of this job, the employee is regularly required to use hands and fingers to handle, feel, or operate objects, tools or controls, and reach with hands and arms. The employee is frequently required to stand, talk and hear.

What do we offer?

We provide competitive and comprehensive benefits to ouremployees.Beloware some highlights of our benefits:

• Medical, Dental, and Vision Insurance Options
• Life and Disability Insurance
• Paid Time-Off
• Parental Benefits
• 401k with Company Match
• Employee Stock Purchase Plan

Learn more about Revvity's benefits by visiting ourpage.

*For benefit-eligible roles only. Part-time and temporary roles may not be eligible for all benefits listed. Please reach out to your recruiter for more information.