Top 13 Manufacturing associate upstream Jobs in Seven Trees Ca

Associate Scientist I / II
Bionova Scientific LLC —Fremont, CA
- $85,000 - $100,000 a year
- Full-time
- Bachelor of Science
- Mid-level
- Bachelor's degree
- Health savings account
- Health insurance
Quick Apply
1d
Manufacturing Associate - Upstream
Asahi Kasei —Fremont, CA
- $25 - $30 an hour
- Weekends as needed
- Mid-level
- Analysis skills
- Training & development
- Health insurance
- Dental insurance
Associate Scientist I / II
Asahi Kasei —Fremont, CA
- $85,000 - $100,000 a year
- Full-time
- Bachelor of Science
- Mid-level
- Bachelor's degree
1d
Training Specialist - Day Shift
Hyve Solutions —Fremont, CA
- $25 - $28 an hour
- Full-time
- Background check
- Microsoft Excel
- Microsoft Outlook
- Health savings account
- Health insurance
Quick Apply
10d
Training Specialist - Swing
Hyve Solutions —Fremont, CA
- $25 - $28 an hour
- Full-time
- Background check
- Microsoft Excel
- Microsoft Outlook
- Health savings account
- Health insurance
Quick Apply
10d
Associate Director, Clinical Supplies-Global Planning & Operations
Summit Therapeutics —Palo Alto, CA
- $175,000 - $200,000 a year
- 5 years
- Engineering
- Mentoring
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Associate Manager, Semi Service
Tesla —Newark, CA
- $108,000 - $162,000 a year
- Full-time
- System design
- Mid-level
- Driver's License
- Commuter assistance
- Health savings account
2d

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Associate Scientist I / II

Bionova Scientific LLC -
Fremont, CA

Quick Apply

Job Details

Full-time
$85,000 - $100,000 a year
1 day ago

Benefits

Health savings account
Health insurance
Dental insurance
401(k)
Paid time off
Vision insurance
401(k) matching
Life insurance

Qualifications

Immunological assays
Defect resolution root cause analysis
Immunological laboratory techniques
Defect analysis
High-performance liquid chromatographs
Protein analysis (analytical chemistry specialty)
Equipment malfunction troubleshooting
Biochemical laboratory techniques
Pharmaceutical analysis
Capillary electrophoresis
Mass spectrometers (MS)
Verification of laboratory test methods
Cross-functional collaboration
Test validation method
Cross-functional communication
Failure analysis

Full Job Description

Bionova, an Asahi Kasei company, is seeking an experienced Associate Scientist to perform analytical testing to support process development, process characterization studies, and stability studies. The associate scientist will participate in development, optimization, and possibly qualification of analytical test methods.

Location: Fremont, California

Company Summary:

Bionova is a rapidly growing, biologics CDMO focused on developing and manufacturing recombinant protein products using mammalian cell culture processes. Our business success is built on bringing together top scientific talent, arming them with the best available tools, and setting them loose in an agile, energized culture focused on solving difficult client problems. Because our success depends on our ability to exceed our clients' expectations, we look for candidates with an innate desire to serve. Adaptability and an interest in transformative action are also common attributes among our team.

Essential Duties and Responsibilities:

Develop, optimize, qualify, and validate analytical test methods such as UV-Vis, HPLC/UPLC, CE, icIEF, ELISA, CBAs, Octet, qPCR, mass spectrometry, and many others.
Perform analytical testing to support cell line development, upstream and downstream process development, formulation development, process characterization studies, and stability studies.
Author technical documents such as method development reports, feasibility reports, method transfer protocols/reports, method validation and qualification protocols/reports, and regulatory filing documents per project needs.
Draft SOPs for laboratory and assay procedures. Prepare concise, sound scientific presentations of study results to the management team and external clients.
Support the investigation of CMC issues and non-conformities to products that impact their safety and efficacy.
Evaluate new technologies and innovations to improve operational efficiency or expand department capabilities.
Support QC in method transfer, analyst training and troubleshooting during method qualification and testing. Assist in client audits and inspections from regulatory agencies, as needed.
Interpret analytical data to support a variety of initiatives and make recommendations for best courses of action as they pertain to drug development.

Working Conditions:

This position requires working in a lab/office setting. The role requires walking, standing, stooping, kneeling, and crouching. The employee must occasionally lift and or move up to 20 pounds independently.

Qualifications:

BS or MS in Biological Sciences or related disciplines with 2+ years of relevant research and/or industry experience in Analytical development, Formulation development, or Quality Control.
In-depth understanding of protein chemistry and industry-standard analytical tools (CE, HPLC/UPLC, Mass Spec, ELISA, qPCR assays, compendial assays, etc.)
Hands-on experience in running, developing, qualifying, and validating analytical methods.
Ability to troubleshoot assay failure related to equipment or execution and identify root cause.
Creative thinker that can identify better and more efficient methods to address issues and gaps.
Demonstrate ability to work independently and on cross-functional teams.
Strong attention to detail.
Effective verbal and written communication skills.
Enthusiastic learner.

The base compensation range for this role is $85,000-$100,000. Base Compensation is influenced by many factors including, but not limited to: time in the role, previous experience, skills, knowledge, performance, work requirements, internal equity, and business / economic conditions.

#LI-MG1

Benefits:

401(k)
401(k) matching
Dental insurance
Health insurance
Health savings account
Life insurance
Paid time off
Vision insurance

Application Question(s):

Do you have a BS or MS in Biological Sciences or related disciplines with 2+ years of relevant research and/or industry experience in Analytical development, Formulation development, or Quality Control? Please explain.
Do you have in-depth understanding of protein chemistry and industry-standard analytical tools (CE, HPLC/UPLC, Mass Spec, ELISA, qPCR assays, compendial assays, etc.)? Please explain.
Do you have hands-on experience in running, developing, qualifying, and validating analytical methods?

Ability to Commute:

Fremont, CA 94538 (Required)

Work Location: In person

Quick Apply

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manufacturing associate upstream jobs in seven trees ca

Associate Scientist I / II

Manufacturing Associate - Upstream

Associate Scientist I / II

Training Specialist - Day Shift

Training Specialist - Swing

Associate Director, Clinical Supplies-Global Planning & Operations

Associate Manager, Semi Service

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