Job Title: Chemist

Job Description

We are seeking a skilled Chemist to join our team. The successful candidate will follow approved GMP manufacturing directions to produce GMP materials, perform in-process testing, and related activities. You will formulate, process, and analyze blends according to schedule, ensuring timely release of quality products. Additionally, you will compile and analyze test information, ensure compliant documentation, and assist in writing or revising GMP documents as needed. Instrument maintenance and calibration, as well as routine maintenance and organization of work areas, are also part of the role. You will work collaboratively with cross-functional counterparts to ensure efficient quality formulations, adhere to SOPs, quality system requirements, safety standards, and regulations, and participate in continual improvement activities.

Responsibilities

• Follow approved GMP manufacturing directions such as Batch Records, Standard Operation Procedures, and Standard Test Procedures.
• Formulate, process, and analyze blends according to schedule; ensure timely release of quality products to avoid backorder.
• Compile and analyze test information; ensure proper reporting and compliant documentation of lot-controlled ingredients.
• Assist in writing or revision of standard operation procedures, batch records, in-process procedures, raw material specifications, and other related GMP documents.
• Perform instrument maintenance and calibration as necessary.
• Routinely maintain and organize work areas and other designated areas at the manufacturing facility.
• Assist or perform incoming raw material testing as needed.
• Confer with functional and cross-functional counterparts to ensure efficient quality formulations.
• Adhere to related Standard Operating Procedures (SOPs), quality system requirements, safety standards, and regulations.
• Participate in continual improvement activities throughout the Manufacturing function to enhance processes, products, and standards.
• Perform other duties as assigned.

Essential Skills

• Experience in reagent preparation, buffer preparation, and formulations.
• Proficiency in using HPLC (High-Performance Liquid Chromatography).
• Bachelor’s degree in Chemistry or equivalent.
• Minimum of one (1) to three (3) years of related experience in a regulated medical device or pharmaceutical environment.
• Detailed knowledge of chemistry and related scientific principles.
• Ability to implement proper techniques and to modify and/or extend theory and practices.
• Good writing, documentation, communication, interpersonal, and analytical skills.
• Computer literacy, including knowledge of Microsoft Office and experience with large enterprise resource planning (ERP) and electronic data management systems.

Additional Skills & Qualifications

• Good problem-solving skills.

Work Environment

The work schedule is from 4:30 AM to 1:30 PM, Monday to Friday. The role involves working in a manufacturing facility where maintaining and organizing work areas is essential. You will adhere to safety standards and regulations, and engage in continual improvement activities to enhance processes, products, and standards.

Pay and Benefits

The pay range for this position is $25.00 - $35.00/hr.

Eligibility requirements apply to some benefits and may depend on your job classification and length of employment. Benefits are subject to change and may be subject to specific elections, plan, or program terms. If eligible, the benefits available for this temporary role may include the following:

• Medical, dental & vision
• Critical Illness, Accident, and Hospital
• 401(k) Retirement Plan – Pre-tax and Roth post-tax contributions available
• Life Insurance (Voluntary Life & AD&D for the employee and dependents)
• Short and long-term disability
• Health Spending Account (HSA)
• Transportation benefits
• Employee Assistance Program
• Time Off/Leave (PTO, Vacation or Sick Leave)

Workplace Type

This is a fully onsite position in San Diego,CA.

Application Deadline

This position is anticipated to close on Feb 12, 2025.

About Actalent

Actalent is a global leader in engineering and sciences services and talent solutions. We help visionary companies advance their engineering and science initiatives through access to specialized experts who drive scale, innovation and speed to market. With a network of almost 30,000 consultants and more than 4,500 clients across the U.S., Canada, Asia and Europe, Actalent serves many of the Fortune 500.

Diversity, Equity & Inclusion

At Actalent, diversity and inclusion are a bridge towards the equity and success of our people. DE&I are embedded into our culture through:

• Hiring diverse talent
• Maintaining an inclusive environment through persistent self-reflection
• Building a culture of care, engagement, and recognition with clear outcomes
• Ensuring growth opportunities for our people

The company is an equal opportunity employer and will consider all applications without regard to race, sex, age, color, religion, national origin, veteran status, disability, sexual orientation, gender identity, genetic information or any characteristic protected by law.

If you would like to request a reasonable accommodation, such as the modification or adjustment of the job application process or interviewing process due to a disability, please email actalentaccommodation@actalentservices.com for other accommodation options.

Salary : $25 - $35