Biopharmaceutical Manufacturing Associate at Randstad

Position Biopharmaceutical Manufacturing Associate
Posted 30 May 2026
Expired 29 Jun 2026
Company Randstad
Location Thousand Oaks | US
Job Type Full Time

Job Description:

Latest job information from Randstad for the position of Biopharmaceutical Manufacturing Associate. If the Biopharmaceutical Manufacturing Associate vacancy in Thousand Oaks matches your qualifications, please submit your latest application or CV directly through the updated Jobkos job portal.

Please note that applying for a job may not always be easy, as new candidates must meet certain qualifications and requirements set by the company. We hope the career opportunity at Randstad for the position of Biopharmaceutical Manufacturing Associate below matches your qualifications.

Job DescriptionJob Description

The Manufacturing Associate I is responsible for executing all manufacturing department processes while strictly adhering to cGMP, environmental health and safety guidelines and any other related regulations that could apply. The Manufacturing Associate I is expected to fully participate in both departmental projects and any quality working teams that may be applicable. This position shall be responsible for the hands on execution of activities as they relate to the manufacturing of products. All of the specific requirements presented in this job description are applicable to the functional area in which it resides. Essential Duties & Responsibilities Clean, Set up, operate, and teardown of equipment in the department such as tanks, filtration systems, room sanitization, etc. Complete relevant paperwork following GDP/GMP guidelines

salary: $21 - $23 per hour
shift: First
work hours: 6:30 AM - 4:30 PM
education: High School

Responsibilities

Qualifications Understanding and compliance in Standard Operating Systems, Current Good Manufacturing Processes (cGMP) & Good Documentation (GDP). Knowledge of basic laboratory and pharmaceutical production equipment including but not limited to: autoclaves, process tanks, incubators, analytical equipment and CIP/SIP systems Must be able to read, write and converse in English. Must be able to read and follow detailed written instructions and have good verbal/written communication skills. Must be proficient in a variety of mathematical disciplines and be able to work with both the metric and US standards of measurement. Must have good interpersonal skills and be able to work effectively and efficiently in a team environment. Must be able to work in a clean room environment wearing special garments. Additionally, personal protective equipment must be worn due to safety requirements. May require immunization before performing work within the manufacturing area. Must have a basic scientific understanding of microbiology, chemistry, sterility, and lyophilization as it applies to the manufacturing process. Must have working knowledge of basic aseptic practices. Must have the knowledge and ability to use a personal computer, electronic mail systems and navigate and conduct searches on the intranet.

The essential functions of this role include:

  • working in a smoke free environment
  • wearing steel toe shoes
  • manual lifting up to 30lbs
  • standing for 10 hours at one time
  • working up to 8 hrs of overtime per week
  • working weekends


Skills

  • Manufacturing
  • Upstream
  • Downstream
  • Biology
  • GMP


Qualifications

  • Years of experience: 1 year
  • Experience level: Entry Level


Randstad is a world leader in matching great people with great companies. Our experienced agents will listen carefully to your employment needs and then work diligently to match your skills and qualifications to the right job and company. Whether you're looking for temporary, temporary-to-permanent or permanent opportunities, no one works harder for you than Randstad.


Equal Opportunity Employer: Race, Color, Religion, Sex, Sexual Orientation, Gender Identity, National Origin, Age, Genetic Information, Disability, Protected Veteran Status, or any other legally protected group status.
At Randstad, we welcome people of all abilities and want to ensure that our hiring and interview process meets the needs of all applicants. If you require a reasonable accommodation to make your application or interview experience a great one, please contact .
Pay offered to a successful candidate will be based on several factors including the candidate's education, work experience, work location, specific job duties, certifications, etc. In addition, Randstad offers a comprehensive benefits package, including: medical, prescription, dental, vision, AD&D, and life insurance offerings, short-term disability, and a 401K plan (all benefits are based on eligibility).
This posting is open for thirty (30) days.
Qualified applicants in San Francisco with criminal histories will be considered for employment in accordance with the San Francisco Fair Chance Ordinance.
Qualified applicants with arrest or conviction records will be considered for employment in accordance with the Los Angeles County Fair Chance Ordinance for Employers and the California Fair Chance Act.
We will consider for employment all qualified Applicants, including those with criminal histories, in a manner consistent with the requirements of applicable state and local laws, including the City of Los Angeles' Fair Chance Initiative for Hiring Ordinance.

Job Info:

  • Company: Randstad
  • Position: Biopharmaceutical Manufacturing Associate
  • Work Location: Thousand Oaks
  • Country: US

How to Submit an Application:

After reading and understanding the criteria and minimum qualification requirements explained in the job information Biopharmaceutical Manufacturing Associate at the office Thousand Oaks above, immediately complete the job application files such as a job application letter, CV, photocopy of diploma, transcript, and other supplements as explained above. Submit via the Next Page link below.

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