Job Ref: 214265743

Date: 2021-07-22 16:54:48

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QC Analytical Chemist
Our client based in Milton Keynes is a global health care leader with a diversified portfolio of prescription medicines, vaccines and animal health products. Today, they are building a new kind of healthcare company – one that is ready to help create a healthier future for all of us.
Their ability to excel depends on the integrity, knowledge, imagination, skill, diversity and teamwork of an individual like you. To this end, they strive to create an environment of mutual respect, encouragement and teamwork. As part of their global team, you’ll have the opportunity to collaborate with talented and dedicated colleagues while developing and expanding your career.
The role is a 1 year temporary contract position initially signed off until August 2022 and offers an hourly rate of up to £23.59 per hour, plus 25 days holiday pro rata and pension scheme. The successful candidate will be required to work onsite in Milton Keynes.
Currently QC is looking for an enthusiastic and dedicated analyst to –
* To support analytical method validation / improvements and method transfers between sites. Drive change management for changing product specifications, supporting Regulatory with changes to product testing. Assist with routine analysis if required.
Key Accountabilities and Duties:
* Experience in Analytical Chemistry techniques is essential. You should have a sound understanding of basic scientific principles.
* Analytical Chemistry method validation / improvements and test transfer between labs/sites.
* Drive change management for introduction of new / improved methods and validation of new equipment.
* Be able to produce technical documents such as protocols, testing and execution plans and final reports. Ability to work on several projects simultaneously and be able to prioritise.
* Liaise with several departments – technical support groups, QA, Regulatory to drive project completion and deliver on milestones.
* The candidate will be required to report all laboratory activities in a clear, organised manner, in the form of reports, following the standard operating procedures.
* Good understanding and ability to perform efficient lab investigations arising from deviations or invalid/atypical results.
* The candidate should be able to provide training to staff on Analytical methods and equipment usage.
* Additionally, the candidate may be required to support laboratory investigations, perform troubleshooting exercises and participate in proof of principle studies.
* Reporting and investigation of OOS and OOT results, determine root causes and implementing effective CAPA actions.
* Perform project related literature searches.
* Interact closely with fellow scientists and global/regional colleagues within own and other departments.
* Work in a multi-disciplinary and international team and environment.
Other responsibilities
Comply with Standard Operational Procedures (SOP’s), GMP, ESH procedures and company corporate policies and process improvements.
Maintain all documentation and training records as per GMP requirements.
To comply with company’s health and safety practices and procedures.
Ensure positive, timely and effective communication with team members and internal customers.
Knowledge:
Spectrophotometric Analyses (FTIR, UV/VIS), TOC
Wet Chemistry techniques including microwave digestions and complexometric titrations
GMP Compliance
Biological testing such as ELISAs, gel electrophoresis knowledge desirable
Experience:
Minimum 3 years background in Pharmaceutical QA/Analytical
Lead Validation and method development and Raw Materials testing including pharmacopoeia
Laboratory investigations
Previous roles include interaction with other operations and technical roles desirable
Skills and Abilities:
MS Word and Excel, Protocol and Report writing, Ability to problem solve
Basic Statistical understanding such as Minitab Statistical software an advantage
Personal Attributes:
Able to communicate at all levels and across all functions, ability to communicate concise technical information with clarity
Ideal candidate should be self-motivated, be able to work under pressure to deliver success within set timelines and hold a positive mindset
Able to assist in Fact finding discussions, flexible approach to changing priorities & attention to detail
Qualifications:
Degree in Applied Chemistry
Other Requirements:
Fluent in English Speaking/writing and cross functional work experience
Full Drivers Licence

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