Biochemist I – GMP

About Us

Revvity is a developer and provider of end-to-end solutions designed to help scientists researchers and clinicians solve the worlds greatest health challenges. We pair the enthusiasm of an industry disruptor with the experience of a longtime leader. Our team of 11000 colleagues from around the globe are vital to our success and the reason were able to push boundaries in pursuit of better human health.

Find your future at Revvity

The Biochemist I GMP position will be responsible for the different stages of manufacturing various BioLegends regulated product produced in our US FDA registered cGMP manufacturing facility.

This role will be responsible for formulating and vialing completing batch records putting away finished good inventory (FGI) data entry equipment maintenance and supply inspections & storage. Other responsibilities include buffer preparation and inspection of incoming buffers into the GMP suite as well as material preparation for Lyophilization and post lyophilization processes.

This role will prepare product/project related documentation and maintain the device history records for all the regulated products and will work closely with product development on new products in order to establish a smooth transition into manufacturing.

Applicants must be currently authorized to work in the United States on a full-time basis for any employer.

The Biochemist I GMP will work independently and as a team player. The ideal candidate will be organized and detail oriented have strong communication skills and is able to work in a very fast paced environment.

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 regulated products which includes filling capping and labeling.
• Assist in troubleshooting the manufacturing process.
• Maintain batch records and other documentations in compliance with ISO13485:2016 and cGMP.
• Maintain/troubleshoot laboratory equipment and manage supplies.
• Perform data entry tasks including processing production orders.
• Work as a team to advance multiple projects simultaneously
• Other projects or responsibilities may be required.

Minimum Qualifications Education and Experience

• Bachelors degree with 1-year biotechnology industry experience.
• 1 year of working experience with Good Documentation Practices (GDP)

Preferred Qualifications Education and Experience

• Bachelors degree in: Biology Biochemistry Chemistry or other related areas
• Working experience in the Biotechnology industry with quality system knowledge including ISO 13485 or cGMP regulation is a plus.
• 1 year of experience in a laboratory and/or biotech manufacturing environment performing filling bottling and packaging.
• Advanced pipetting skill is highly preferred.
• Familiarity with raw material supply receiving and inspection processes.
• Excellent verbal and written communication skills
• Demonstrated knowledge of aseptic techniques in biosafety cabinet
• Demonstrated ability to work well in small groups and adhere to timelines.
• Excellent attention to detail and organizational skills

The base salary range for this full-time position is $26.44-$29.00/hour. 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 our 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 Revvitys benefits by visiting ourBswiftpage. 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.

Revvity is an equal opportunity employer. All qualified applicants will receive consideration for employment without regard to any characteristic or status protected by applicable federal state and/or local laws. If you are an applicant with a disability that requires reasonable accommodation to complete any part of the application process or are limited in the abilityor unable to usethe online application system and need an alternative method for applying you may contact.