Associate Manufacturing

Kelly Services-Portugal; Juncos (PR); On-site; USD 18,000 - 25,000; Full time

Benefits offered by this job

Career opportunities

Career guides

3,000 online training courses

Bi-weekly pay

Other benefits

Job summary

AtKelly SETT, a leading biotech staffing partner, is seeking an Associate Manufacturing to work with a top biotechnology client in the East area of PR. The role involves hands-on operations, media prep, and GMP-compliant manufacturing in a fast-paced environment.

Qualifications include a Bachelor in Sciences and experience with lab equipment, GMP, and manufacturing. We offer exposure to multiple client opportunities, training resources, and bi-weekly pay through Kelly PR.

Qualifications

• Bachelor's degree in Biotechnology, Microbiology, Biology, or Chemistry.
• Experience with lab equipment and computers.
• GMP environment and manufacturing experience.

Responsibilities

• Hands-on operations, set-up, cleaning, sanitizing and prepare media and buffers per procedures.
• Perform and monitor critical processes.
• Execute routine validation protocols.
• Draft and revise routine GMP documents (MPs, SOPs, and technical reports).
• Initiate quality incidents.
• Identify and implement improvements after approval.
• Basic troubleshooting.

Skills

Lab equipment experience

Computers

GMP experience

Education

Bachelor in Sciences (Biotechnology, Microbiology, Biology, Natural Sciences, Chemistry)

Job description

AtKelly®Science,Engineering,Technology&Telecom(SETT),we’repassionateabouthelpingyoufindajobthatworksforyou.Howaboutthisone?

We’reseekinganAssociateManufacturingtoworkwithoneofourtopbiotechnologyindustryclientsintheEastareaofPR.

Salary:$15.50 p/h (plusshiftdifferential)
Schedule: Available to work any shift / 12 hrs shift (5:00am to 5:30pm and 5:00pm to 5:30am)

Responsibilities:

• Hands-on operations, set-up, clean, sanitize and prepare media and buffers per procedures.
  
• Perform and monitor critical processes.
  
• Execute routine validation protocols.
  
• Comply with GMP’s5. Regularly draft and revise routine documents (e.g. MPs, SOP’s, and technical reports)
  
• Initiate Quality incidents
  
• Identify and recommend improvements related to routine functions and implement after approval
  
• Basic troubleshooting

Qualifications:

• Bachelor in Sciences (Biotechnology, Microbiology, Biology, Natural Sciences, Chemistry)
  
• Experience with lab equipment and computers
  
• Experience in GMP environment and manufacturing area.

Kelly PR Offers!

• Exposure to a variety of career opportunities as a result of our expansive network of client companies
  
• Career guides, information and tools to help you successfully position yourself throughout every stage of your career
  
• Access to more than 3,000 online training courses through our Kelly Learning Center
  
• Bi -weekly pay
  
• Among other benefits!