Analytical Lab Analyst, Fixed Term Contract

at  Imperial Brands

Liverpool, England, United Kingdom -

Start DateExpiry DateSalaryPosted OnExperienceSkillsTelecommuteSponsor Visa
Immediate26 May, 2024Not Specified01 Mar, 20242 year(s) or aboveCommunication Skills,Regulatory Standards,Method Development,Pharmaceutical Sciences,Chemistry,Gxp,Analytical Skills,ValidationNoNo
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Description:

PRINCIPLE ACCOUNTABILITIES

  • Perform routine/non-routine analysis in a safe and timely manner, adhering to current ways of working e.g., GxP/GLP requirements.
  • Perform research and regulatory non-routine analysis in a safe and timely manner, always adhering to current legislative requirements.
  • Actively participate in problem solving and root cause analysis.
  • Organize & perform all routine/non-routine work & solve technical issues.
  • Produce & maintain all relevant documents such as written reports, validation documents, SOP’s and records.
  • Organise & maintain laboratory stock levels.
  • Operate lab related software.
  • Organise individual projects.
  • Provide monthly updates on projects undertaken.
  • Ensure & foster good working relationships between technical functions to allow laboratory requirements to be shared and understood by all areas.
  • Support the introduction and validation (VP, URS, DQ, FST, SAT, IQ, OQ, PQ, VR & VC) of new/existing equipment in accordance with ICH guidelines.
  • Develop & validate analytical methods for new or existing products or services in accordance with ICH guidelines.
  • Adhere to all business policies & procedures.
  • Support development of new/junior analysts, as required and perform any other tasks as required by the line manager and/or business.

SKILLS AND EXPERIENCE REQUIRED

Essential

  • Practical knowledge of HPLC, GC & Pharmacopeia analysis is essential.
  • In-depth knowledge of method and equipment validation processes in accordance with ICH guidelines
  • Demonstrate the ability to implement procedures & processes which ensure compliance to GxP and other relevant regulatory standards.
  • Excellent oral & written communication skills.
  • Strong technical, analytical, report and writing skills.
  • Decisive thinker able to work within agreed timescales.
  • Understanding of statistical techniques.
  • At least +2 years’ experience of analytical method development and equipment / method validation within an analytical laboratory / regulated laboratory.
  • Area of expertise preferred: Method Development, Validation, Regulatory and/or Nicotine products.
  • Degree or higher in Chemistry, Pharmaceutical Sciences, or related scientific discipline is desirable.

Desirable

  • Good level of IT skills.
  • Demonstrate the ability to organise individual projects in line with department priorities.
  • Ability to work against challenging timelines.
  • Excellent analytical skills.

ABOUT US

We’re a truly international company, fourth largest in our industry and operating across 119 markets. An inclusive, innovative global FMCG business supported by 25,000 employees. As we embrace a new era of growth, we are transforming. Our ways of working and culture are driven by a challenger mindset, constantly questioning the status quo where people can bring their best selves to work. Our agility and collaboration are driving our ambitions, innovation and success all supported by our award-winning development programmes that creates exciting and rewarding career opportunities for all. Encouraging inclusion at local levels and supporting a developing and robust diversity agenda globally, we’re fully committed to creating and maintaining an environment that celebrates and respects difference

Responsibilities:

2 Year – Fixed Term Contract
You will provide direct support to the Laboratory Manager (and/or deputy) in all day-to-day aspects of the analytical lab department and ensure that all methods and equipment used, are scientifically sound and fulfil the quality requirements appropriate for the respective business requirement. You will support the lab function and ensure accurate/timely analysis for routine and non-routine products and check/validate all analysis performed and be highly competent in all analytical techniques undertaken.


REQUIREMENT SUMMARY

Min:2.0Max:7.0 year(s)

Pharmaceuticals

Pharma / Biotech / Healthcare / Medical / R&D

Clinical Pharmacy

Graduate

Chemistry pharmaceutical sciences or related scientific discipline is desirable

Proficient

1

Liverpool, United Kingdom