Analytical Chemical Process Development Scientist
at Eurofins UK PSS
Liverpool, England, United Kingdom -
Start Date | Expiry Date | Salary | Posted On | Experience | Skills | Telecommute | Sponsor Visa |
---|---|---|---|---|---|---|---|
Immediate | 10 Feb, 2025 | Not Specified | 10 Nov, 2024 | N/A | Mass Spectrometry,Collaboration,Chemistry,Electronic Media | No | No |
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Description:
EUROFINS PSS INSOURCING SOLUTIONS® IS A GLOBAL, AWARD-WINNING INSOURCING SOLUTION. WE PLACE OUR SKILLED TEAM DIRECTLY AT THE CLIENT SITE, MANAGING OPERATIONS SEAMLESSLY AND ELIMINATING COMPLEXITIES. WE ENSURE A STRATEGIC, LONG-TERM SERVICE COMMITMENT THAT DELIVERS VALUE DIRECTLY AT THE CLIENT’ SITE, UTILISING THEIR FACILITIES, EQUIPMENT, AND METHODOLOGIES, WHILE MAINTAINING THE SAME SERVICE, EXPERTISE, AND CGMP COMPLIANCE AVAILABLE AT THE EUROFINS FACILITY. IF YOU’RE AN EMPLOYEE SEEKING AN EXCEPTIONAL CAREER JOURNEY, EUROFINS PSS INSOURCING SOLUTIONS® IS YOUR GATEWAY TO A FUTURE WHERE INNOVATION, COLLABORATION, AND SUCCESS CONVERGE. JOIN US IN A WORLD WHERE EXCELLENCE KNOWS NO BOUNDARIES!
Job Description
QUALIFICATIONS
- A degree in Chemistry or a closely aligned discipline is required.
- A sound, fundamental knowledge of Chemistry, particularly organic chemistry/small molecules is essential.
- A minimum of 2 years’ relevant experience of pharmaceutical analysis preferably in a method development role, is essential.
- Experienced and competent with modern instrumental equipment (HPLC, Mass Spectrometry, Karl Fischer etc).
- Able to interpret raw data from multiple sources `and draw conclusions regarding troubleshooting of instruments and methods.
- A thorough understanding of chromatographic techniques, both practical and theoretical is essential.
- A thorough understanding of requirements for working in a GMP environment would be beneficial.
- The ability to quickly learn new processes and work proactively to offer suggestions for new ways to improve existing processes would be desired.
- Must be able to work using fully electronic media, including MS Office.
- Requires the ability to form strong working relationships with colleagues.
- Needs to be able to work on own initiative and be capable of developing solutions to problems as part of a team.
- Must be willing to operate in a flexible manner and be able to switch priorities at short notice. Seeks new ideas to make improvements within own area of control.
Additional Information
Responsibilities:
The purpose of this job is to perform analysis of pharmaceutical raw materials, drug substance, and finished product and produce accurate results within an acceptable timeframe.
- To perform routine and non-routine analysis using traditional and modern analytical techniques, as required by the Lead Analyst or customer representative.
- To review analytical data for GMP compliance.
- To initiate and follow-up OOS results and action limits as per customer procedures.
- To participate in the preparation of reports.
- To document data as dictated by current client policies and procedures.
- To collect and measure productivity through agreed metrics such as number of tests performed, cycle times, lab/product issues, number of hours worked per project, etc.
- Ensure that the customer gets the best possible service by continually reviewing best practice in relation to both commercial and quality issues and ensuring 100% ethical work standards and GMP compliance.
- To prepare and approve results for tests in which they have received the appropriate training and are deemed competent.
- To understand and be constantly aware of the customer’s requirements and strive to meet or exceed those requirements keeping in mind the customer process end points.
- To deal with customer queries and contact designated personnel, with appropriate support from onsite leadership, with any relevant information or issues relating to test results or the service in general.
- Support local audits as required,
- To perform testing in accordance with customer procedures.
- To revise SOPs as required by the Lead Analyst.
- To keep the laboratory area clean and tidy in both ‘seen’ and ‘unseen’ areas.
- To provide cover for other members of staff as required and for taking part in the customer’s weekend rota and/or overtime schedule.
- To ensure that all documentation is carried out on time, is accurate and legible and conforms to the relevant quality standards. Must be able to mentor junior members of the team with this regard.
- To ensure that the customer’s requirements are fully met or exceeded and in so doing will be flexible to work in any area of the business as is required.
REQUIREMENT SUMMARY
Min:N/AMax:5.0 year(s)
Pharmaceuticals
Pharma / Biotech / Healthcare / Medical / R&D
Clinical Pharmacy
Graduate
Chemistry
Proficient
1
Liverpool, United Kingdom