QC Biologist
- Recruiter
- Confidential
- Location
- Milton Keynes
- Salary
- 18.00 - 21.00 GBP Annual
- Posted
- 09 Jun 2022
- Closes
- 07 Jul 2022
- Sectors
- Health, Nursing & Social Care
- Contract Type
- Temporary
- Hours
- Full Time
QC Biologist
Our client is a global health care leader with a diversified portfolio of prescription medicines, vaccines and animal health products based in Milton Keynes. 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.
We have an opportunity for a QC Biologist to join their QC Team. The role is a full-time temporary contract role initially signed off for 9 months with a possible extension. The role offers an hourly rate of GBP18.00 - GBP21 per hour depending on experience, plus 25 days holiday pro rata.
Purpose of the Role:
Currently QC is looking for an enthusiastic and dedicated analyst to -
* To support method validation / improvements and method transfers for Biology and Microbiology labs between sites.
* Support activities in the areas of qualification of critical reagents (biomaterials) used in Bio-assays, such as ELISA coats, ELISA conjugates, reference sera, toxins etc.
Key Accountabilities and Duties:
* Expertise in Immunology techniques such as ELISA's, haemagglutination tests, antigen mass assay is essential.
* Biology/Microbiology method validation / improvements and test transfer between labs/sites.
* Production and Validation and of biomaterials used in in-process and final product testing.
* Understanding of microbiology techniques is beneficial.
* Support in 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.
* Update SOP's and other GMP documents ensuring they are current and relevant.
* Ability to work on several projects simultaneously and be able to prioritise.
* Reporting and communication of results to stakeholders. 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.
* Reporting and investigation of OOS and OOT results, determine root causes and implementing effective CAPA actions.
* 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.
The above list of duties is not exhaustive and is subject to change. The post holder may be required to undertake other duties within the scope and grading of the post.
Person Specification:
Knowledge:
* Good understanding and working knowledge of GMP Quality Systems
* Technical expertise in ELISA's and other immunology techniques, including microbiology techniques.
Experience:
* Minimum 3 years of experience with excellent understanding of testing within a laboratory environment
* Laboratory investigations
* Validation and method development
* Previous roles include interaction with other operations and technical roles desirable
Skills and Abilities:
* Proficient in use of Microsoft Office especially Excel and Word.
* Good Protocol and Report writing skills.
* Ability to troubleshoot to resolve issues
* Basic Statistical understanding Knowledge such as Minitab Statistical software
Personal Attributes:
Ideal candidate should be self-motivated, hardworking, be able to work under pressure to deliver success within set timelines and hold a positive mindset
Excellent organisational and planning skills and a flexible approach to changing priorities
Able to communicate concise technical information with clarity, at all levels and across all functions
Able to assist in fact finding discussions
Attention to detail
Qualifications:
Degree in Biology/Microbiology
Other Requirements:
Cross functional work experience
Demonstrated scientific problem-solving capabilities
Full UK driving licence
Our client is a global health care leader with a diversified portfolio of prescription medicines, vaccines and animal health products based in Milton Keynes. 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.
We have an opportunity for a QC Biologist to join their QC Team. The role is a full-time temporary contract role initially signed off for 9 months with a possible extension. The role offers an hourly rate of GBP18.00 - GBP21 per hour depending on experience, plus 25 days holiday pro rata.
Purpose of the Role:
Currently QC is looking for an enthusiastic and dedicated analyst to -
* To support method validation / improvements and method transfers for Biology and Microbiology labs between sites.
* Support activities in the areas of qualification of critical reagents (biomaterials) used in Bio-assays, such as ELISA coats, ELISA conjugates, reference sera, toxins etc.
Key Accountabilities and Duties:
* Expertise in Immunology techniques such as ELISA's, haemagglutination tests, antigen mass assay is essential.
* Biology/Microbiology method validation / improvements and test transfer between labs/sites.
* Production and Validation and of biomaterials used in in-process and final product testing.
* Understanding of microbiology techniques is beneficial.
* Support in 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.
* Update SOP's and other GMP documents ensuring they are current and relevant.
* Ability to work on several projects simultaneously and be able to prioritise.
* Reporting and communication of results to stakeholders. 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.
* Reporting and investigation of OOS and OOT results, determine root causes and implementing effective CAPA actions.
* 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.
The above list of duties is not exhaustive and is subject to change. The post holder may be required to undertake other duties within the scope and grading of the post.
Person Specification:
Knowledge:
* Good understanding and working knowledge of GMP Quality Systems
* Technical expertise in ELISA's and other immunology techniques, including microbiology techniques.
Experience:
* Minimum 3 years of experience with excellent understanding of testing within a laboratory environment
* Laboratory investigations
* Validation and method development
* Previous roles include interaction with other operations and technical roles desirable
Skills and Abilities:
* Proficient in use of Microsoft Office especially Excel and Word.
* Good Protocol and Report writing skills.
* Ability to troubleshoot to resolve issues
* Basic Statistical understanding Knowledge such as Minitab Statistical software
Personal Attributes:
Ideal candidate should be self-motivated, hardworking, be able to work under pressure to deliver success within set timelines and hold a positive mindset
Excellent organisational and planning skills and a flexible approach to changing priorities
Able to communicate concise technical information with clarity, at all levels and across all functions
Able to assist in fact finding discussions
Attention to detail
Qualifications:
Degree in Biology/Microbiology
Other Requirements:
Cross functional work experience
Demonstrated scientific problem-solving capabilities
Full UK driving licence