US
0 suggestions are available, use up and down arrow to navigate them
PROCESSING APPLICATION
Hold tight! We’re comparing your resume to the job requirements…
ARE YOU SURE YOU WANT TO APPLY TO THIS JOB?
Based on your Resume, it doesn't look like you meet the requirements from the employer. You can still apply if you think you’re a fit.
Job Requirements of Scientist II:
-
Employment Type:
Contractor
-
Location:
Carlsbad, CA (Onsite)
Do you meet the requirements for this job?
Scientist II
Careers Integrated Resources Inc
Carlsbad, CA (Onsite)
Contractor
Job Title: Scientist II
Job Location: Carlsbad, CA
Job Duration: 12 Months+ (Temp to perm)
Shift Timing: Monday- Friday (8 am to 4 pm)
Pay range: $30 - 35/hr on w2.
Job Description:
Minimum Qualifications:
Skills:
Preferred Qualifications:
#sczr2
Job Location: Carlsbad, CA
Job Duration: 12 Months+ (Temp to perm)
Shift Timing: Monday- Friday (8 am to 4 pm)
Pay range: $30 - 35/hr on w2.
Job Description:
- Work in a team-based environment and perform antibody purification for use in research and commercial scientific products for the life sciences industry.
- Experiments are performed following controlled protocols and data is recorded on batch records following good documentation practices.
- Key Objectives of the role: Responsible for manufacturing the product(s) in a lab setting following standard operating procedures.
- Will utilize basic laboratory techniques, calculations, materials measurement, operation of laboratory equipment, and record-keeping necessary to manufacture products.
- Will perform purification using AKTA, HPLC, and in-process testing through SDS-Page.
- Responsible for Batch Data Records, notebooks, customer reports, and work order documents.
- Utilize specialized technical knowledge and skills to make detailed observations and analyze data to ensure within operating parameters. Advise the manager of factors that may affect the quality of the product. Suggest options/ideas for corrective actions.
- Maintain equipment, product inventories, and related records as assigned. Note variances on manufacturing documents; audit and evaluate process documents and propose revisions.
- Complete, distribute, and file records as required in accordance with Document Control Practices.
- Identify potential issues in the qualification process; report findings to team management and members for resolution or participate in troubleshooting. May lead process improvement projects. Complete, distribute, and file records; prepare ad hoc reports as requested.
- May perform other related duties as required and/or assigned. Advise the team lead/manager of factors that may affect quality of the product, initiate problem reports for deviations and non-conforming materials, and suggest options and ideas for corrective actions and preventive actions (CAPA).
Minimum Qualifications:
- Bachelor's degree in Biology, Molecular Biology, Biochemistry, Biotechnology or other related discipline and 2+ years of experience in a manufacturing or research laboratory.
- Plus: Masters. Degree in Biology, Molecular Biology, Biochemistry, Biotechnology, or other related discipline and some experience in a manufacturing or research laboratory.
- Experience in the use of scientific laboratory techniques, equipment, and materials that include some of the following techniques: AKTA purification of antibodies, SDS-page testing, and HPLC analysis. Ability to carry out scientific procedures and make recommendations for improvement.
Skills:
- Excellent documentation and communication skills. Displays positive attitude toward job and others.
- Regularly required to lift up to 20 pounds. May be required to lift weight of 45 pounds or more, with assistance and/or with equipment on occasion.
- Must be flexible to work varying schedules and hours as needed. Must be able to work safely with chemicals and hazardous materials.
- May be required to stand for long periods of time while performing duties.
- May intermittently sit at desk/lab bench for a long period of time to perform experiments, write, and use a keyboard to communicate through written means.
Preferred Qualifications:
- Ability to work independently/in a group setting with direct supervision.
- Works on assignments that are moderately complex in nature where judgment is required in resolving problems and making routine recommendations.
- Experience in ISO 90001, ISO 13485, and/or GMP manufacturing environment.
- Good problem-solving skills.
#sczr2
Get job alerts by email.
Sign up now!
Join Our Talent Network!