Associate Scientist Job at Amgen (South San Francisco)

Associate Scientist

Join Amgen’s Mission of Serving Patients. At Amgen, if you feel like you’re part...

Location

United States of America , South San Francisco

Salary:

110633.00 - 140020.00 USD / Year

Amgen

Expiration Date

Until further notice

Requirements

Associate Degree or equivalent in Biological Science program with at least 3 years of histology laboratory experience
HT (ASCP) or HLT (ASCP) preferred
Experience in histopathology / pathobiology in an industry setting
Hands-on experience in a variety of histology-based methodologies and equipment
Experience in documentation, including laboratory information management systems usage
Comfortable working in a dynamic environment designed to promote frequent interaction and brainstorming
Ability to manage multiple projects simultaneously
Excellent communication skills

Job Responsibility

Perform workflows for histology preparation of specimens, including all documentation in required laboratory information systems and databases, as well as team communications
Perform basic and advanced histology procedures (fixation and processing of tissues, embedding, microtomy, H&E staining, special stains, coverslipping, slide scanning, slide QC)
Review work to ensure accuracy and to ensure adherence to pertinent departmental policies, practices, and procedures
Ensure equipment is functional and maintained in good working order, and that lab safety protocols are adhered to
Perform all other related duties as assigned

What we offer

Retirement and Savings Plan with generous company contributions
group medical, dental and vision coverage
life and disability insurance
flexible spending accounts
discretionary annual bonus program
stock-based long-term incentives
award-winning time-off plans
flexible work models where possible

Fulltime

Associate Scientist

The primary purpose of this job role is to function as a member of the Sample Lo...

Location

United States , Pearl River

Salary:

60200.00 - 97500.00 USD / Year

Pfizer

Expiration Date

Until further notice

Requirements

Bachelor of Science Degree or Bachelor of Arts Degree in a relevant scientific discipline with 0-2 years of experience in the pharmaceutical industry
Knowledgeable with Microsoft applications including Word Processing, Excel, and PowerPoint
Ability to work in a team setting

Job Responsibility

Receive samples from global clinical/study trials according to approved protocols and processes
Participate in all aspects of tracking and documenting the chain of custody of samples
Perform sample receipt, documentation, storage, tracking, aliquoting, distribution to the testing labs, and sample disposal
Complete all processes as detailed in Sample Logistics and Solutions Standard Operating Procedures
Perform job responsibilities in compliance with GXP and all other regulatory agency requirements
Receive samples from clinical trial sites and enter samples into an electronic database management system
Perform sample storage and retrieval using manual freezers and BiOS (automated freezer storage system)
Perform manual sample aliquoting and aliquoting using the Hamilton robotic instrument
Ship samples and lab supplies to external and internal testing labs
Assist in the general maintenance of the Hamilton robotic instruments

What we offer

Participation in Pfizer’s Global Performance Plan with a bonus target of 7.5% of the base salary
401(k) plan with Pfizer Matching Contributions and an additional Pfizer Retirement Savings Contribution
Paid vacation, holiday and personal days
Paid caregiver/parental and medical leave
Health benefits to include medical, prescription drug, dental and vision coverage
Relocation assistance may be available based on business needs and/or eligibility

Fulltime

New

Associate Scientist I

This is where new knowledge is discovered. Baxter’s Research and Development tea...

Location

India , Bengaluru

Salary:

Not provided

Baxter

Expiration Date

Until further notice

Requirements

Knowledge of small molecules analytical projects
Organizational skills with demonstrated attention to detail
Ability to apply a logical and methodical approach to analytical and quality processes and to formulate sound recommendations
Good understanding of GMP standards in a laboratory environment
Ability to work on multiple tasks simultaneously while meeting deadlines
Strong interpersonal skills with the ability to collaborate effectively within cross-functional teams
Quality-oriented mindset
Master in Science degree (e.g. Analytical Chemistry, Organic chemistry, Biochemistry, Bio-engineering, Pharmaceutical Science)
Minimum of 2-6 years of experience in pharmaceutical industry (R&D, manufacturing…)
Demonstrated expertise in reviewing analytical chemistry data (e.g. experiments, reports)

Job Responsibility

Maintain schedules for periodic reviews of test method assays in collaboration with the management and analytical SMEs. Monitor tasks progress and identify potential planning risks
Manage change control activities related to test method assay periodic reviews and updates in accordance with project needs and agreed timelines
Contribute to R&D analytical activities by reviewing experiments within her/his area of technical expertise
Support analytical projects through effective collaboration in documentation management
Contribute to the continuous improvement of quality processes within R&D analytical laboratories

What we offer

Support for Parents
Continuing Education/ Professional Development
Employee Heath & Well-Being Benefits
Paid Time Off
2 Days a Year to Volunteer

Clinical Scientist Associate Director – Late Development, Oncology

Join Amgen's Mission of Serving Patients. At Amgen, if you feel like you're part...

Location

Portugal , Lisbon

Salary:

79656.90 - 107771.10 EUR / Year

Amgen

Expiration Date

Until further notice

Requirements

Doctorate degree and 3 years of life sciences/healthcare experience
Master's degree and 5 years of life sciences/healthcare experience
Bachelor's degree and 7 years of life sciences/healthcare experience

Job Responsibility

Support set up and execution of late phase clinical trials with a focus on data quality
Assist in authoring clinical protocols, Investigators Brochures and other regulatory documents ensuring consistency and clarity
Provide input into and implementation of data management plan, CRF design, and data review oversight
Support review, analysis, and presentation preparation of clinical trial data for internal decision making, external interactions, and regulatory submission
Assists the management of collaborators, consultants, and/or Clinical Research Organizations in completion of key projects
Anticipate and actively manage problems across a broad spectrum of cross-functional teams
Work cross-functionally within teams to ensure clinical strategy is translated into the development of the study concept document, study protocol and related documents
Support appropriate training, recruitment, and development requirements for matrix team resources

What we offer

Comprehensive employee benefits package, including a Retirement and Savings Plan with generous company contributions, group medical, dental and vision coverage, life and disability insurance, and flexible spending accounts
Discretionary annual bonus program, or for field sales representatives, a sales-based incentive plan
Stock-based long-term incentives
Award-winning time-off plans
Flexible work models, including remote and hybrid work arrangements, where possible

Fulltime

Associate Scientist - II, R&D - SPO

This is where new knowledge is discovered. Baxter’s Research and Development tea...

Location

India , Ahmedabad

Salary:

Not provided

Baxter

Expiration Date

Until further notice

Requirements

Master's in Pharmaceutics or equivalent
Hands on experience in laboratory batch execution and drive the towards the expected result
Good communication skills for effective liaison and teamwork
Problem-solving skills, analytical skills and attention to detail
Excellent organizational skills and the ability to work on several tasks or projects concurrently
Presentation skills - for presenting ideas and findings to colleagues and customers
Ability to work well independently, with minimum supervision
Drive, enthusiasm and self-motivation
An aptitude for mathematics and statistics and highly developed IT and technical skill
Postgraduate with minimum 07 years of experience in pharmaceutical industry preferably in formulation development

Job Responsibility

Actively Support launch and sustenance of Baxter commercial products globally by following the Baxter Quality Management Systems
Assist in the management of the Baxter product design throughout the product lifecycle and maintenance of the product DHF, or similar product design governance documents for a particular product family
Identify and analyze design problems to achieve optimal solutions that satisfy cost and technical requirements. Formulate new, innovative approaches to solve technical problems on a consistent basis
Actively involve in commercialized product investigation, execute batches in laboratory, prepare report to support the investigation
Involve in compendial product change/proposal discussion, assess the proposed change impact on the product quality & patient safety. Provide support to analytical team by providing the required product solution/placebo solution samples. Execute batches in laboratory, assess the study outcome to support the compendial product change requirement
Ensure response to customer queries, agencies query, market compliance. Design and execute batches/experiments in laboratory, prepare report to support queries/market compliance
Responsible for ensuring the availability of required licenses and materials (raw material, packaging materials) in laboratory

What we offer

Support for Parents
Continuing Education/ Professional Development
Employee Heath & Well-Being Benefits
Paid Time Off
2 Days a Year to Volunteer

Fulltime

Associate Scientist - II, R&D - SPO

This is where new knowledge is discovered. Baxter's Research and Development tea...

Location

India , Ahmedabad

Salary:

Not provided

Baxter

Expiration Date

Until further notice

Requirements

Master's in Pharmaceutics or equivalent
Postgraduate with minimum 07 years of experience in pharmaceutical industry preferably in formulation development
Hands on experience in laboratory batch execution and drive the towards the expected result
Good communication skills for effective liaison and teamwork
Problem-solving skills, analytical skills and attention to detail
Excellent organizational skills and the ability to work on several tasks or projects concurrently
Presentation skills - for presenting ideas and findings to colleagues and customers
Ability to work well independently, with minimum supervision
Drive, enthusiasm and self-motivation
An aptitude for mathematics and statistics and highly developed IT and technical skill

Job Responsibility

Actively Support launch and sustenance of Baxter commercial products globally by following the Baxter Quality Management Systems
Assist in the management of the Baxter product design throughout the product lifecycle and maintenance of the product DHF, or similar product design governance documents for a particular product family
Identify and analyze design problems to achieve optimal solutions that satisfy cost and technical requirements
Formulate new, innovative approaches to solve technical problems on a consistent basis
Actively involve in commercialized product investigation, execute batches in laboratory, prepare report to support the investigation
Involve in compendial product change/proposal discussion, assess the proposed change impact on the product quality & patient safety
Provide support to analytical team by providing the required product solution/placebo solution samples
Execute batches in laboratory, assess the study outcome to support the compendial product change requirement
Ensure response to customer queries, agencies query, market compliance
Design and execute batches/experiments in laboratory, prepare report to support queries/market compliance

What we offer

Support for Parents
Continuing Education/ Professional Development
Employee Heath & Well-Being Benefits
Paid Time Off
2 Days a Year to Volunteer

Fulltime

Associate Scientist - Oncology

Amgen Oncology Research is seeking an Associate Scientist who supports our T cel...

Location

United States , South San Francisco

Salary:

98299.10 - 132992.90 USD / Year

Amgen

Expiration Date

Until further notice

Requirements

Master's Degree
Bachelor's Degree and 2+ years of relevant experience
Associate's degree and 4 years of relevant experience
High school diploma / GED and 6 years of relevant experience

Job Responsibility

Support preclinical pipeline programs by performing assays and delivering scientific evidence of drug candidates in a timely manner
Operate and maintain standard lab equipment
Maintain organized laboratory notebooks and repositories
Interact closely with cross-functional team
Support publication and presentation at scientific conferences

What we offer

Comprehensive employee benefits package including Retirement and Savings Plan with generous company contributions, group medical, dental and vision coverage, life and disability insurance, and flexible spending accounts
Discretionary annual bonus program
Stock-based long-term incentives
Award-winning time-off plans
Flexible work models where possible

Fulltime

Associate Scientist – In Vivo Pharmacology, Oncology

At Amgen, if you feel like you’re part of something bigger, it’s because you are...

Location

United States , South San Francisco

Salary:

98299.10 - 132992.90 USD / Year

Amgen

Expiration Date

Until further notice

Requirements

Master’s degree and 2+ years of experience in in-vivo work with rodents
OR Bachelor’s degree and 4+ years of experience in in-vivo work with rodents
OR High school diploma / GED and 6 years of experience in in-vivo work with rodents

Job Responsibility

Carry out hands-on in vivo work in mice, including handling, tumor inoculation and measurement, dosing (oral, SC, IP, and IV), blood and tissue collection, and health monitoring
Perform necropsies and support ex vivo tissue activities, including dissection, processing, sample preparation, and experimental readouts
Perform in vitro work including multiparametric flow cytometry and molecular biology techniques associated with in vivo studies
Strong communication to support study execution, maintain accurate study records, and present results
Active participation and presentation at cross-departmental teams and meetings
Participate in dosing rotations, including occasional evening or weekend work

What we offer

health and welfare plans for staff and eligible dependents
financial plans with opportunities to save towards retirement or other goals
work/life balance
career development opportunities
Retirement and Savings Plan with generous company contributions
group medical, dental and vision coverage
life and disability insurance
flexible spending accounts
discretionary annual bonus program
stock-based long-term incentives

Fulltime

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