Not SpecifiedCompensation
Junior (1 to 2 years)Experience Level
Full TimeJob Type
UnknownVisa
PharmaceuticalIndustries

Requirements

  • Degree in Chemistry or strongly related scientific field
  • At least 2 years relevant industrial experience
  • Ability to apply GMP regulations and other international guidelines to all aspects of the position
  • Ability to work independently and adhere to critical timelines
  • Excellent attention to detail

Responsibilities

  • Support new equipment qualification, lab computerized system and chemistry lab set up
  • Perform transfer/verification/validation of laboratory procedures within the team where required
  • Prepare technical documentation including but not limited to protocols, analytical write-ups, standard operating procedures, specifications, investigations and reports
  • Perform analysis of incoming goods, intermediates and/or finished products (including HPLC and GC) under cGMP conditions for QC release or as part of stability studies
  • Review analytical and laboratory data within the department for accuracy, completeness and compliance with documented procedures
  • Perform planned preventative maintenance and performance calibrations on equipment
  • Management of QC chemical, reference standard and consumable stock levels
  • Maintain own training records
  • Communicate optimally with others on site
  • Participate/contribute in Practical Process Improvement initiatives (PPI) or continuous improvement in the lab
  • Support and encourage a “Quality Culture” and company 4i values throughout QC
  • Ensure cGMP is applied in their area of work and align with cGMP in all areas of the business
  • Work with HSE, cGMP and 5S in mind at all times
  • Undertake ad-hoc activities that may be required by the business
  • Support shift work (if necessary) in future
  • Understand emergency procedures and align with safe systems of work
  • Ensure compliance with environment, health and safety and security policies and procedures, rules, signage and instructions at all times
  • Ensure prompt reporting and investigation of all accidents, near misses and breaches of rules

Skills

HPLC
GC
cGMP
GMP
Method Validation
Method Transfer
Method Verification
SOP
Technical Documentation
Equipment Qualification
Data Review
Stability Studies
Laboratory Analysis

Thermo Fisher Scientific

Provides life sciences products and services

About Thermo Fisher Scientific

Thermo Fisher Scientific offers a variety of products and services that support scientific research and healthcare, including laboratory equipment, reagents, and software solutions. Their products are used in applications like protein biology, real-time PCR, and sequencing, serving clients such as academic institutions and pharmaceutical companies. Unlike competitors, Thermo Fisher emphasizes customer support and education, helping clients optimize their experiments. The company's goal is to be a leading provider of life sciences solutions that contribute to a healthier and safer world.

Waltham, MassachusettsHeadquarters
1956Year Founded
$17MTotal Funding
IPOCompany Stage
Biotechnology, HealthcareIndustries
10,001+Employees

Risks

Increased competition in single-use bioprocessing may impact market share.
Sale of anatomical pathology business could create a temporary product gap.
Investment in miDiagnostics may face regulatory challenges affecting returns.

Differentiation

Thermo Fisher offers a comprehensive range of life sciences products and services.
Their well-known brands include Thermo Scientific, Applied Biosystems, and Invitrogen.
They provide strong customer support and educational resources to optimize client workflows.

Upsides

Expansion of biologics production facility enhances capacity for precision biologics monitoring.
Investment in miDiagnostics aligns with demand for rapid diagnostic solutions in BioPharma.
Collaboration with Mainz Biomed positions them in the growing cancer detection market.

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