Process Development Chemist

BioLegend, Inc.; Hopkinton (MA); On-site; USD 66,000 - 85,000; Full time

Benefits offered by this job

Medical, Dental, Vision Insurance

Life and Disability Insurance

Paid Time-Off

Parental Benefits

Compassionate Care Leave

401k with Company Match

Employee Stock Purchase Plan

Job summary

BioLegend, Inc. in Hopkinton, MA seeks a Process Development Chemist to manufacture reagents per SOPs and quality standards, coordinating with reagent planning, dispensing and QA teams to ensure consistent reagent performance for downstream workflows.

You will collaborate with R&D on troubleshooting and process improvements, while supporting scale-up, documentation, and continual optimization of manufacturing processes.

Qualifications

• Bachelor's degree in life or natural sciences; 2 years of laboratory experience.
• 1 year of experience with basic computer skills (Microsoft Word, Excel, Teams) for data analysis and documentation.
• Experience with GMP, SOPs, quality documentation practices.

Responsibilities

• Manufacture reagents according to SOPs and GMP requirements.
• Execute QC testing of raw materials and final products and document results.
• Maintain accurate records and prepare for audits and quality reviews.
• Setup, calibration, and maintenance of laboratory equipment.
• Collaborate with R&D and production to troubleshoot and improve processes.
• Support scale-up and process validation activities.
• Participate in inventory control and material handling.
• Assist with change control and batch documentation reviews.
• Ensure compliance with safety and regulatory standards.
• Label, dispense, and package reagents as needed.

Job description

Job Summary:

As a Process Development Chemist, you will manufacture reagents according to SOPs and applicable quality and manufacturing requirements, ensuring reagent consistency, working alongside reagent planning, dispensing, and quality assurance teams. You will have the opportunity to collaborate with cross‑functional teams, including R&D, for troubleshooting, continuous improvement, and implementing novel processes to support consistent reagent performance for downstream laboratory workflows.

Key Responsibilities:

• Execute product manufacturing according to established procedures (SOPs) using good manufacturing practice (GMP).
• Manufacture products in alignment with quality and safety requirements (ISO 9001/14001/45001).
• Execute QC testing of raw materials and final products and document results per established procedures.
• Maintain strong laboratory practices, including accurate recordkeeping with a readiness for audits and quality reviews.
• Support general lab functions, setup, calibration, and maintenance of equipment.
• Collaborate with scientists and production teams to troubleshoot issues, refine standard work, and support scale‑up and process validation activities.
• Support reagent manufacturing through change control activities, batch documentation reviews, and continuous improvement initiatives.
• Participate in inventory receipt, maintenance, and control of raw materials, products, and lab supplies.
• Facilitate investigations, recording, and implementation of product deviations or CAPA systems.
• Independently troubleshoot and resolve routine issues using established procedures, escalating complex issues as needed.
• Work safely and in compliance with all applicable company, federal and local regulations.
• May be required to label, dispense, and package reagents and final products.

The key responsibilities listed in this job description are intended only as illustrations of the various types of work that may be performed. The omission of specific statements of duties does not exclude them from the position if the work is similar, related, or a logical assignment to the position.

Basic Qualifications:

• Bachelor’s degree in life or natural sciences discipline
• 2 years of laboratory experience.
• 1 year of experience with basic computer skills (Microsoft suite including Word, Excel, and Teams) for data analysis, record‑keeping, and document maintenance.

Preferred Qualifications:

• Good project management, organization skills, and attention to detail and accuracy; maintain good laboratory documentation practices; ability to handle multiple projects or tasks in a fast‑paced environment.
• Experience with reagent or chemical manufacturing workflows, including tech transfer or production support is highly desired but not required.
• Familiarity with method validation concepts and routine quality documentation practices.
• Familiarity with applicable analytical tools including UV-Vis, fluorometers, or similarly related equipment.
• Experience with electrophoretic analysis relevant to proteins, DNA, and/or RNA (or strong capability to learn and apply these techniques quickly).
• Demonstrates strong interpersonal skills (verbal and written communication) and is enthusiastic to work with and provide support in a cross‑functional team environment.
• Problem solver, with a positive, proactive, can‑do attitude; knows when to ask for help and how to help others.
• Willingness to learn new concepts, challenge boundaries, and adjust to changing priorities effectively.

Physical Requirements:

• May require the ability to lift 25 pounds and stand for long periods of time.

The key responsibilities listed in this job description are intended only as illustrations of the various types of work that may be performed. The omission of specific statements of duties does not exclude them from the position if the work is similar, related, or a logical assignment to the position.

Compensation Range:

The annual base salary range for this full‑time position is $65,500 - $85,000. 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.

What do we offer?

We provide competitive and comprehensive benefits to our employees. Below are some highlights of our benefits:

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

Learn more about Revvity’s benefits by visiting our Bswift page. Log‑In instructions are provided towards the bottom of the Bswift page.

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.