Job Title: Chemist
Job Description

We are seeking a dedicated Chemist to join our team. The successful candidate will follow approved GMP manufacture directions such as Batch Records, Standard Operation Procedures, Standard Test Procedures, and other procedures to manufacture GMP materials, perform in-process tests, and related activities. This role involves formulating, processing, and analyzing blends according to schedule, ensuring the timely release of quality products to stock to avoid backorder situations.

ResponsibilitiesFollow approved GMP manufacture directions including Batch Records, Standard Operation Procedures, and Standard Test Procedures.Manufacture GMP materials and perform in-process tests.Formulate, process, and analyze blends as per the schedule.Ensure the timely release of quality products to stock to avoid backorder.Compile and analyze test information, ensuring proper reporting and compliant documentation of lot-controlled ingredients.Assist in writing or revising standard operation procedures, batch records, in-process procedures, raw material specifications, and other related GMP documents.Perform instrument maintenance and calibration as necessary.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 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 SkillsExperience with reagent preparation, buffer preparation, and formulations.Proficiency in High-Performance Liquid Chromatography (HPLC).Bachelor’s degree in Chemistry or equivalent.Minimum of one (1) to three (3) years of related experience, preferably within a regulated medical device or pharmaceutical environment.Detailed knowledge of chemistry and related scientific principles.Ability to implement proper techniques and modify 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 & QualificationsGood problem-solving skills.Experience in a regulated environment is preferred.Work Environment

The work schedule is Monday to Friday, 4:20 AM to 1:00 PM. The role involves working in a manufacturing facility where adherence to safety standards and regulations is essential. Employees are expected to maintain and organize their work areas and follow all relevant Standard Operating Procedures (SOPs) and quality system requirements. The company offers a competitive benefits package including an 8% 401K match, various health plan packages, accrued PTO of 15 days once permanent, and three floating holidays.

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 18, 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.