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职位Thermo Fisher

Scientist III (LCMS Pharma)

Thermo Fisher

Scientist III (LCMS Pharma)

Thermo Fisher

Athlone, Ireland

·

On-site

·

Full-time

·

2mo ago

必备技能

LCMS

Method Validation

Method Transfer

Analytical Testing

Data Analysis

Work Schedule

Standard (Mon-Fri)

Environmental Conditions

Adherence to all Good Manufacturing Practices (GMP) Safety Standards

Job Description

Scientist III - LCMS - Pharma:

At Thermo Fisher Scientific, you’ll discover meaningful work that makes a positive impact on a global scale. Join our colleagues in bringing our Mission to life - enabling our customers to make the world healthier, cleaner and safer. We provide our teams with the resources needed to achieve individual career goals while taking science a step beyond through research, development and delivery of life-changing therapies. With clinical trials conducted in 100 countries and ongoing development of novel frameworks for clinical research through our PPD clinical research portfolio, our work spans laboratory, digital and decentralized clinical trial services. Your determination to deliver quality and accuracy will improve health outcomes that people and communities depend on – now and in the future.

Location/Division Specific Information

Our PPD® Laboratory Services team has a direct impact on improving patient health through the expertise of scientists, industry thought-leaders and therapeutic guides. As the world leader in serving science, our laboratory professionals bring their commitment to accuracy and quality to deliver groundbreaking innovations. This position will be based at our GMP Laboratory in Athlone providing testing services to our clients.

Discover Impactful Work:

The role of Scientist III - LCMS is to perform complex laboratory analysis of pharmaceutical products and proficiently uses analytical instrumentation, calculates and analyses data and records data. Routinely acts as the project leader on multiple projects, interacts with clients, reviews and evaluates data, writes reports and protocols. Responsible for the scientific conduct of the project and communication of regulatory issues with senior level team members.

A day in the Life:

  • Independently performs method validations, method transfers and analytical testing of pharmaceutical compounds in a variety of formulations.

  • Designs and completes experiments with minimal supervision.

  • Prepares study protocols, project status reports, final study reports and other project-related technical documents.

  • Communicates data and technical issues to the client and responds to client needs

  • Mentors, trains and coordinates laboratory activities of other team members and assists in troubleshooting instruments and analytical problems.

  • Assists in designing method validation or method transfer protocols and establishing project timelines.

  • Reviews data for technical, quality and compliance to protocols, methods, SOPs, client criteria and Good Manufacturing Practices (GMP).

Keys to Success:

Education & Experience

  • Educated to a bachelor's degree level in a relevant area, ie chemistry, biochemistry

  • 5 years’ relevant industry experience within a GMP laboratory with experience handling various types of LCMS instrumentation for example LCMS-QQQ/Sciex 6500 or similar, Orbitrap or other high resolution LCMS instrumentation and with complex data evaluation and processing

  • Experience in Method Validation, Method Transfer and Analytical testing.

In some cases an equivalency, consisting of a combination of appropriate education, training and/or directly related experience, will be considered sufficient for an individual to meet the requirements of the role.

Knowledge, Skills, Abilities

  • Detailed knowledge of method validation; method development would be an advantage.

  • The ability to plan, schedule and carry out work for successful project completion

  • A positive attitude and ability to work well with others

  • Excellent attention to detail

  • Our Mission is to enable our customers to make the world healthier, cleaner and safer. Watch as our colleagues explain 5 reasons to work with us. As one team of 100,000 colleagues, we share a common set of values

  • Integrity, Intensity, Innovation and Involvement - working together to accelerate research, solve complex scientific challenges, drive technological innovation and support patients in need. #Start Your Story with PPD, part of Thermo Fisher Scientific, where diverse experiences, backgrounds and perspectives are valued.

Apply today! http://jobs.thermofisher.com

Thermo Fisher Scientific is an EEO/Affirmative Action Employer and does not discriminate on the basis of race, color, religion, sex, sexual orientation, gender identity, national origin, protected veteran status, disability or any other legally protected status.

Accessibility/Disability Access

Job Seekers with a Disability: Thermo Fisher Scientific offers accessibility service for job seekers requiring accommodations in the job application process. For example, this may include individuals requiring assistance because of hearing, vision, mobility, or cognitive impairments. If you are a job seeker with a disability, or assisting a person with a disability, and require accessibility assistance or an accommodation to apply for one of our jobs, please submit a request by telephone at 1-855-471-2255. Please include your contact information and specific details about your required accommodation to support you during the job application process.

This telephone line is reserved solely for job seekers with disabilities requiring accessibility assistance or an accommodation in the job application process. Messages left for other purposes, such as not being able to get into the career website, following up on an application, or other non-disability related technical issues will not receive a response.

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关于Thermo Fisher

Thermo Fisher

Thermo Fisher Scientific Inc. is an American life science and clinical research company. It is a global supplier of analytical instruments, clinical development solutions, specialty diagnostics, laboratory, pharmaceutical and biotechnology services.

10,001+

员工数

Waltham

总部位置

$200B

企业估值

评价

3.0

10条评价

工作生活平衡

3.5

薪酬

3.8

企业文化

3.2

职业发展

3.5

管理层

2.1

45%

推荐给朋友

优点

Good benefits and compensation

Nice people to work with

Learning opportunities and skill development

缺点

Poor management and leadership issues

Disengaged or unsupportive management

Frequent reorganizations and chaos

薪资范围

2,092个数据点

Mid/L4

Mid/L4 · BIOPROCESS DEVELOPMENT SCIENTIST

2份报告

$118,049

年薪总额

基本工资

$91,146

股票

-

奖金

-

$118,049

$118,049

面试经验

8次面试

难度

3.0

/ 5

时长

14-28周

录用率

12%

体验

正面 12%

中性 63%

负面 25%

面试流程

1

Application Review

2

Recruiter Screen

3

Hiring Manager Interview

4

Panel Interview

5

Final Interview

6

Offer

常见问题

Technical Knowledge

Behavioral/STAR

Past Experience

Culture Fit

Industry Specific