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职位Thermo Fisher

Scientist III (Pharma)

Thermo Fisher

Scientist III (Pharma)

Thermo Fisher

Athlone, Ireland

·

On-site

·

Full-time

·

2mo ago

必备技能

HPLC

UPLC

Mass Spec

UV Spectrometry

Data Analysis

Technical Writing

Work Schedule

Standard (Mon-Fri)

Environmental Conditions

Adherence to all Good Manufacturing Practices (GMP) Safety Standards

Job Description Scientist III - 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 role will be based at our GMP Laboratories in Athlone, Ireland and will work within a team specifically working with Oligonucleotides.

Discover Impactful Work:

The role of Scientist III is to perform a variety of complex sample preparation and analysis procedures to quantitatively measure small molecules using a wide range of analytical instrumentation. Working mainly independently, Scientists will interpret analytical data in regard to acceptability and consistency and set up and maintain analytical instrumentation.

A day in the Life

  • Perform a variety of complex sample preparations

  • Analysis procedures to quantitatively measure pharmaceutical compounds in a variety of formations for stability testing and other studies for analytical testing support

  • Review and compilation of results

  • Performing work assignments accurately, timely and in a safe manner

  • Training on routine operation, maintenance and theory of analytical instrumentation, SOPs, and regulatory procedures and guidelines.

  • Works with multiple functional groups to meet business needs.

  • Sets up and maintains analytical instrumentation.

  • Trains on routine operation, maintenance and theory of analytical instrumentation, SOPs and regulatory procedures and guidelines.

  • Ensures QA findings are addressed appropriately.

  • Communicates project status to project leader.

  • Performs work assignments accurately, and in a timely and safe manner.

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

Education and Experience

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

  • 5 years’ relevant industry experience within a GMP laboratory

  • The applicant should have a 5 years’ analytical experience with

  • Proficient in Waters and Agilent HPLC and UPLC

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

  • HPLC

  • Mass Spec

  • UV spectrometry, pH, Dissolution, Osmolality, Karl Fisher

  • Proven ability to interpret data by performing trend analysis

  • Proven technical writing skills

  • Proven problem solving skills

  • 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

  • The ability to write protocols and reports with minimum supervision

  • Excellent attention to detail

  • Be able to communicate effectively and follow detailed written and verbal instruction

  • 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.

We welcome and encourage applicants from outside of Ireland.  We can provide support with immigration and visa needs for successful applicants and dependents, tax consultations and other basic destination services.  All other relocation costs are at the expense of the applicant.

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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