Job Details

ID #52096625
Estado California
Ciudad Thousandoaks
Full-time
Salario USD TBD TBD
Fuente Actalent
Showed 2024-07-14
Fecha 2024-07-15
Fecha tope 2024-09-13
Categoría Etcétera
Crear un currículum vítae
Aplica ya

Manufacturing Associate - ENTRY LEVEL

California, Thousandoaks, 91358 Thousandoaks USA
Aplica ya

Biopharmaceutical industry leader in Thousand Oaks is looking for a manufacturing associate to join their team! Opportunity to support development and launch of pharmaceutical products in a production environment. ENTRY-LEVEL CANDIDATES ARE WELCOME TO APPLY! REQUIREMENTS:

B.S. in Life Sciences Discipline

Interest in biotech industry

Must be open to working 1st, 2nd, or 3rd shift

WHAT'S IN IT FOR YOU:

Gain experience in a manufacturing environment

Make an impact in patients' lives

Competitive pay

Job SummaryThe Associate of Manufacturing will join our dynamic production team in Thousand Oaks. This role supports development, clinical, and launch activities. Under general supervision, the associate will perform manufacturing operations according to Standard Operating Procedures (SOPs). Responsibilities include:

Hands-on operations: set-up, cleaning, and sanitization of various manufacturing equipment

100% manual inspection per defined manufacturing procedures (MPs) and standard operating procedures (SOPs)

Testing of drug product in-process/release samples per defined methods and SOPs

Following GMP documents (SOPs, MPs) with strict adherence to safety and compliance

Performing and monitoring critical processes with the ability to perform basic troubleshooting

Performing in-process sampling of equipment and operating analytical equipment

Performing inspection activities of filled containers

Maintaining an organized and clean workspace

Working in a GMP room environment, full clean room gowning, hairnet and gloves when performing all work

Initiating quality reports

Drafting and revising documents (SOPs, MPs)

Identifying, recommending, and implementing improvements related to routine functions

Assisting in the review of documentation for assigned functions (equipment logs, batch records)

Performing activities that include periods of rigorous, repetitive work

Working around high-pressure systems and occasionally work around heavy equipment

SkillsGMP, SOP, chemistry, biology, microbiology, pipetting, Bachelor of Science Experience Level Entry Level 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 [email protected] (%[email protected]) for other accommodation options.

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