Production Chemist 1 in San Diego

Energy Jobline ZR; San Diego (CA); On-site; USD 60,000 - 90,000; Full time

Job summary

Connexion is seeking a Production Chemist I for 100% onsite work in San Diego. The role involves manufacturing bulk clinical and commercial kit reagents, sub-assembly formulation, raw material processing, and QC testing in a fast-paced GMP environment.

The candidate must have a science degree, be able to start at 6:30 AM, stand for long periods, lift up to 40 lbs, and wear PPE including an N-95 respirator, with strong attention to SOPs and a collaborative mindset.

Qualifications

• Bachelor's degree in a science-related field (Chemistry, Biology, Biochemistry, Microbiology, or similar).
• Ability to start by 6:30 AM and work onsite.
• Ability to stand for long periods and lift up to 40 lbs.
• Comfortable working around chemicals and manufacturing reagents.
• Willing and able to wear required PPE, including an N-95 or half-face respirator.
• Strong attention to detail and ability to follow SOPs precisely.
• Team-oriented attitude and willingness to work collaboratively.

Responsibilities

• Manufacture bulk clinical and commercial kit reagents.
• Prepare and process raw materials.
• Perform reagent and component formulations.
• Conduct QC and in-process testing.
• Complete ERP transactions and batch documentation.
• Maintain device history records and training documentation.
• Operate laboratory equipment, autoclaves, and CIP systems.
• Support process improvements and manufacturing transfers.
• Follow GMP, quality, and safety requirements at all times.

Skills

Attention to detail

Lean Manufacturing

Teamwork

Education

Bachelor's degree in science

Tools

ERP system

Job description

Job DescriptionJob Description

Connexion’s mission is to provide "best in class" services to job seekers. We strive to achieve excellence in job placement, staffing, and recruiting services, while treating candidates with the professionalism and respect they deserve.

Job Title: Production Chemist I

Shift: M-F 1st Shift 6:30am-3pm

Notes:

• 100% onsite in San Diego, CA
• Occasional overtime and weekend support may be required based on business needs
• Fast-paced GMP manufacturing environment supporting commercial production

Summary of Duties and Responsibilities:

To perform this job successfully, an individual must be able to perform each essential duty satisfactorily. The requirements listed below are representative of basic knowledge, skills, and or abilities required. Reasonable accommodation may be made to enable individuals with disabilities to perform the essential functions.

• Responsible for the manufacture of bulk clinical and commercial kit reagents.
• Responsible for sub-assembly formulation.
• Prepares and or processes raw materials.
• Performs QC testing of reagents, component formulations and some in-process testing.
• Participates in transfer, support activities and continuous improvement on existing processes.
• Maintains detailed device history records and training logs.
• Ensures proper transportation, handling, and disposal of hazardous, bio-hazardous and or infections substances.
• Operates and calibrates all general lab equipment.
• Completes ERP transactions.
• Maintains measures and dispenses materials.
• Operates CIP and or autoclave systems.

Must-Have Requirements:

Do not submit candidates missing any of the following:

• Bachelor's degree in a Science-related field (Chemistry, Biology, Biochemistry, Microbiology, or similar)
• Ability to work onsite and start no later than 6:30 AM
• Ability to stand for extended periods and lift/carry up to 40 lbs.
• Comfortable working around chemicals and manufacturing reagents
• Willing and able to wear required PPE, including an N-95 or half-face respirator for significant portions of the workday
• Strong attention to detail and ability to follow SOPs precisely
• Team-oriented attitude and willingness to work collaboratively

Qualifications:

• GMP manufacturing experience
• Production chemistry experience
• Reagent manufacturing experience
• Laboratory experience
• Experience completing batch records and controlled documentation
• ERP transaction experience
• Lean Manufacturing knowledge

Key Responsibilities:

• Manufacture bulk clinical and commercial kit reagents
• Prepare and process raw materials
• Perform reagent and component formulations
• Conduct QC and in-process testing
• Complete ERP transactions and batch documentation
• Maintain device history records and training documentation
• Operate laboratory equipment, autoclaves, and CIP systems
• Support process improvements and manufacturing transfers
• Follow GMP, quality, and safety requirements at all times