GMP Biochemist I: Formulation, Vialing & Documentation

Revvity, Inc.; San Diego (CA); On-site; USD 28,000 - 37,000; Full time

Benefits offered by this job

Medical, Dental, Vision Insurance

401k with Company Match

Employee Stock Purchase Plan

Paid Time-Off

Job summary

Revvity, Inc. is seeking a Biochemist I – GMP to support multiple stages of manufacturing at our US FDA-registered facility. You will formulate and vial products, prepare buffers, manage batch records, and assist with lyophilization preparation and post-lyophilization steps.

The ideal candidate will be organized, detail-oriented, and capable of thriving in a fast-paced environment while ensuring compliance with GDP, ISO 13485, and cGMP standards.

Qualifications

• Bachelor’s degree with 1-year biotechnology industry experience.
• 1 year of working experience with Good Documentation Practices (GDP).
• Familiarity with ISO 13485 or cGMP regulations is a plus.

Responsibilities

• Prepare buffers for manufacturing activities.
• Perform formulation and vialing of regulated products (filling, capping, labeling).
• Maintain batch records and documentations per ISO13485 and cGMP.
• Troubleshoot the manufacturing process and maintain equipment.
• Work with product development for smooth transition to manufacturing.

Skills

GDP knowledge

Aseptic technique

Detail oriented

Strong communication

Team collaboration

Data entry accuracy

Education

Bachelor’s degree (biology/biochemistry/chemistry)

Job description

Revvity, Inc. is seeking a Biochemist I – GMP to support multiple stages of manufacturing at our US FDA-registered facility. You will formulate and vial products, prepare buffers, manage batch records, and assist with lyophilization preparation and post-lyophilization steps.

The ideal candidate will be organized, detail-oriented, and capable of thriving in a fast-paced environment while ensuring compliance with GDP, ISO 13485, and cGMP standards.