Production Chemist

QuidelOrtho; San Diego (CA); On-site; USD 67,000 - 75,000; Full time

Benefits offered by this job

Comprehensive benefits package

Employee Stock Purchase Plan

Paid time off and holidays

Job summary

QuidelOrtho is searching for a skilled Production Chemist to join our team in San Diego, CA. This role entails operating laboratory equipment and supporting manufacturing goals while adhering to GMP regulations.

The ideal candidate will have experience in a GMP environment, strong problem-solving skills, and a commitment to safety and quality. Competitive salary range of $67,303.53 - $75,000.00, along with comprehensive benefits including medical and 401(k).

Qualifications

• Ability to follow detailed instructions and maintain accurate records.
• Knowledge of a variety of lab equipment and their operation.
• Ability to carry out experiments following established guidelines.

Responsibilities

• Carries out production tasks to meet manufacturing goals.
• Operates laboratory equipment and performs maintenance.
• Ensures materials are appropriately labeled and approved.

Skills

Attention to detail

Problem-solving

Troubleshooting

Teamwork

Communication skills

Education

High School Diploma with 5-8 years of related work in GMP

BA or BS in Chemistry/Biological Sciences with 2-4 years of GMP experience

Master's in Chemistry/Biological Sciences with 0-2 years of GMP experience

Tools

Laboratory equipment

Job description

The Role

At QuidelOrtho, we’re advancing the power of diagnostics for a healthier future for all. Join our mission as our next Production Chemist. Under minimal ongoing supervision, this position is responsible for a variety of manufacturing support functions involving the operation of lab equipment and conduct of procedures/tasks according to established GMP under the direction of senior staff including manufacturing products within QSR and ISO regulations.

This position will be onsite in San Diego, CA.

Responsibilities

• Carries out production tasks in support of manufacturing goals and objectives
• Participates in Lean Initiatives
• Operates laboratory equipment safely, as trained and directed, in accordance with established practices
• Maintains records and notebooks as directed in a neat, thorough and accurate manner. Performs required data entry on company planning and materials management system
• Ensures materials are appropriately labeled, approved for use and in sufficient quantity to complete required tasks
• Reviews/reconciles documents and work orders. Writes/revises documentation as needed
• Supports product transfers
• May train other chemists/lab technicians
• Partners with the planners, provide input into weekly schedule
• Initiates and participates in lead document revisions to ensure accurate BOM's process descriptions, NCMR and deviations
• Operates laboratory equipment and performs routine maintenance/repair
• Follows all safety guidelines, manufacturing policies and procedures. Operates under strict QSR and ISO compliance
• Performs complex formulations, component and material evaluations, equipment calibrations and maintenance
• Formulates complex chemistries and solutions as directed, following established guidelines and procedures
• Carries out duties in compliance with established business policies
• Performs other duties & projects as assigned
• Participates in product/process troubleshooting and validations
• Carries out functions which may require multiple task coordination
• Covers on call assignment and complies with all restrictions and requirements
• Assesses issues affecting departmental performance, Quality standards, and product quality. Individually communicates to management and initiates appropriate corrective action
• Supports departmental troubleshooting, cross-functional projects and process improvement teams
• Perform other work-related duties as assigned

The Individual

Required

• High School Diploma plus 5-8 years of related work experience in a GMP environment, or
• BA or BS in Chemistry, Biological Sciences, and 2-4 years of related experience in a GMP environment, or
• Master’s degree in Chemistry, Biological Sciences, or equivalent and 0-2 years of related experience in GMP environment required
• Ability to follow detailed instructions, maintains accurate records and notes, and carries out assignments in a thorough, conscientious fashion while adhering to safe laboratory practices
• Knowledge of a variety of lab equipment and their operation
• Ability to carry out experiments following established guidelines and summarize results accurately
• Strong problem-solving and troubleshooting skills
• Strong verbal and written communication skills
• Organized and detail oriented
• Ability to work in a team environment
• General computer knowledge
• Understands and is aware of the quality consequences which may occur from the improper performance of their specific job. Has awareness of device defects that may occur in their area of responsibility, including product design, verification and validation, manufacturing and testing activities
• This position is not currently eligible for visa sponsorship.

Preferred

• Previous training and experience in the operation of lab equipment and use of lab chemicals and tools

Key Working Relationships

Manufacturing, Materials, Technical Support and Quality Assurance

The Work Environment

The work environment characteristics are representative of an office, laboratory, and manufacturing environment and include handling of viral and bacterial hazards, potentially hazardous chemicals, as well as infectious or potentially infectious bodily fluids, tissues and samples. Flexible work hours to meet project deadlines.

The Physical Demands

Position requires the ability to lift up to 30 lbs. on a regular basis. Up to 75% of time at lab or production environment, walking, standing, and sitting for long periods of time are routine to accomplish tasks in this role. Specific vision abilities required by this job include close and distance vision and the ability to adjust focus. Must have the ability to operate lab equipment. Position requires use of Personal Protective Equipment as posted.

Salary Transparency

The salary range for this position takes into account a wide range of factors including education, experience, knowledge, skills, geography, and abilities of the candidate, in addition to internal equity and alignment with market data. At QuidelOrtho, it is not typical for an individual to be hired at or near the top range for their role and compensation decisions are dependent on the facts and circumstances of each case. The salary range for this position is $67,303.53 - $75,000.00 and is bonus eligible. QuidelOrtho offers a comprehensive benefits package including medical, dental, vision, life and disability insurance, along with a 401(k) plan, employee assistance program, Employee Stock Purchase Plan, paid time off (including sick time), and paid holidays. All benefits are non‑contractual, and QuidelOrtho may amend, terminate, or enhance the benefits provided, as it deems appropriate.

Equal Opportunity

QuidelOrtho believes in Equal Opportunity for all and is committed to ensuring all individuals, including individuals with disabilities, have an opportunity to apply for those positions that they are interested in and qualify for without regard to race, religion, color, national origin, citizenship, sex, sexual orientation, gender identity, age, veteran status, disability, genetic information, or any other protected characteristic. QuidelOrtho is also committed to providing reasonable accommodations to qualified individuals so that an individual can perform the duties.