Posts Tagged ‘QA’
Tuesday, September 4th, 2012
Reena Dhana at CK Science is currently recruiting for a Qualified Person (QP) to join a Global Pharmaceutical Company based in Surrey on a full time, 3 month contract.
Responsibilities:
As a Qualified Person you will be responsible for documentation control, sign off and batch release of over the counter drugs.
Qualifications:
The successful candidate for this Qualified Person role will hold a chemistry or pharmacy degree (or equivalent), will be on the register of eligible Qualified Persons and named in the appropriate Manufacturer’s Licence. You will also have experience ideally gained in the Pharmaceutical Industry.
How to apply:
Apply online:
For more information or to apply for this role please contact Reena Dhana on 01438 723 500 or email rdhana@ckscience.co.uk. Please quote reference ST25093 in all correspondence.
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Tags: audit, jobs in surrey, Manufacturer's Licence, pharmaceutical jobs, Pharmaceutical jobs surrey, QA, QP, Qualified Person, qualified person jobs, Qualified Person roles surrey, Reena Dhana, science jobs in surrey, Surrey
Posted in Industry News, News | No Comments »
Thursday, July 12th, 2012
Barney Smith at CK Science is recruiting for a Quality Coordinator to work in a food manufacturing company who are a market leader in their field at their site in Glasgow
Responsibilities:
This quality Coordinator position will involve being responsible for planning and carrying out investigative activities relating to customer returns and complaints. You will be involved in a wide range of physical quality tests, providing detailed analysis, interpretation and reporting of results including on-going trend analysis.
Qualifications:
For this Quality coordinator position you must have a proven track record in a similar role within the food manufacturing or related industry, be a self starter and be comfortable working to tight deadlines.
Benefits:
As a Quality Coordinator you will join a company who offer excellent salary packages including annual bonus, life assurance and group personal pension, and generous holiday entitlement. They are a successful company that always look to promote from within and invest training, time and resources to making the best of their employees.
How to apply:
Apply online:
For more information or to apply for this Quality Co-ordinator role please contact Barney Smith on 0191 384 8905 or email bsmith@ckscience.co.uk Please quote reference DH24700 in all correspondence.
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Tags: barney smith, Coordinator jobs, food, food manufacturing job, Glasgow, Glasgow area jobs, jobs in Scotland, manufacturing, QA, quality coordinator, Quality Coordinator in Glasgow, quality jobs, Scotland jobs, scottish jobs
Posted in Jobs, News | No Comments »
Monday, June 18th, 2012
Julie Marshall at CK Science is currently recruiting for a Stability Programme Coordinator to join a QA department for a pharmaceutical company based in Sussex on a full time, temporary basis for 12 months
Responsibilities:
As Stability Programme Coordinator you will be responsible for:
- Requesting, receipt and delivery of stability samples
- The design of Stability Protocols, influencing content and processes and exerting advocacy for regulatory and QMS requirements
- Set up and management of stability studies in electronic (LIMS) systems, including troubleshooting
- Owning the process for preparation, labelling and storage of stability samples within temperature and humidity controlled environmental chambers in accordance with approved protocols and procedures
- Approving and reporting data generated by the laboratories and contributing to the review of laboratory OOS/ OOT investigations and deviations to identify trends and preventative actions
Qualifications and skills:
The successful Stability Programme Coordinator will have the following qualifications, skills & experiences:
- Degree in a relevant subject (or equivalent) or experience in a role that demonstrates technical understanding of equipment and processes
- Comprehensive knowledge of worldwide stability regulations
- Stability data interpretation and use of appropriate tests
- Good understanding of the QMS and change control system in particular
- Knowledge and experience in stability regulations
If successful, you will be joining a global company and in return there is an attractive salary and career progression opportunities.
How to apply:
Apply online:
For more information or to apply for this Stability Programme Coordinator position, please contact Julie Marshall via email jmarshall@ckscience.co.uk or telephone 01438 723 500. Please quote reference ST24533 in all correspondence.
Tags: ck science jobs, Julie Marshall., QA, QMS, quality assurance, science jobs, Stability, Stability Programme, Stability Programme Coordinator, Stability Programme Coordinator jobs, Stability Programmer job
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Monday, June 11th, 2012
Barney Smith at CK Science is recruiting for a QA technician to join one of the most successful and innovative food companies in Scotland
Responsibilities:
As a QA technician you will be working a continental shift pattern and will be responsible for:
- Data collection
- Process auditing
- Completing on line checks with detailed analysis and interpretation of results.
Qualifications:
The successful candidate for this QA technician must be qualified to minimum HNC or equivalent in a Quality Management of Food Science related discipline or equivalent industrial experience and have a proven track record in QA within the food or biotechnology industry.
How to apply:
Apply online:
For more information or to apply for this QA technician role please contact Barney Smith on 0191 384 8905 or email bsmith@ckscience.co.uk. Please quote reference DH24485 in all correspondence.
Tags: barney smith, food industry, food industry jobs, food jobs, jobs in science, jobs in Scotland, manufacturing, QA, QA jobs, QA Technician jobs, QA Technician jobs Scotland, QA Technician roles, quality, technician jobs
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Tuesday, May 29th, 2012
Hannah Milward at CK Science is currently recruiting for a Temporary Site QA Lead to join a pharmaceutical and biotechnology company at their site in the West Midlands
The Job:
A Site Quality Leader is responsible for ensuring quality and regulatory compliance of the facility, while driving process effectiveness and efficiency. The Site Quality Leader represents the company to external agencies and champions the evolution of the quality culture for the site.
Responsibilities:
Key responsibilities of this Site Quality Leader role will include:
- Directing the Site Quality Management System, fully integrated into the Global Quality Management System, including cross-functional and site-specific processes. The role is responsible for facility compliance covering voluntary, regulatory and company quality requirements and will champion quality initiatives at all levels of the organisation.
- Maintaining and improving all aspects of Site Quality Planning.
- Overseeing all Quality-related communications and training requirements for all site employees
- Establishing positive relationships with outside agencies
- Hosting Quality System audits and inspections
- Overseeing the Corrective Action / Preventive Action activities and Complaint Handling Programs, and in some cases, Quality Engineering
- Report on Quality System effectiveness and requirements to management team as required including preparing and executing facility Quality Management Reviews
- Driving the definition of site quality objectives, metrics, reporting and operating mechanisms
- Participating in selected global initiatives to share best practices and leverage quality synergies
- Supporting local R&D programs and quality issue resolution
- Acting as Management Representative for Quality at the Site
- Operates a Local Inspection program and manages f/up activities to close NCs.
Qualifications:
To be considered for this Site QA Lead role you will have:
- A Bachelor’s degree or equivalent in Engineering, Medical Device Technology or Scientific Field
- You will have an understanding of product development, manufacturing, quality control and servicing in the medical equipment or pharmaceutical industry.
- You will also have hands-on experience with FDA, QSR, ISO, MDD and/or other international quality systems requirements.
How to apply:
Apply online:
For more information or to apply for this Site QA Lead role please contact Hannah Milward on 0114 283 9956 or email hmilward@ckscience.co.uk. Please quote reference SH24376 in all correspondence.
Tags: CK Science, FDA, hannah milward, ISO, MDD, QA, QA Assurance, QA Site leader, QSR, quality assurance, science, science jobs, Site QA Lead - West Midlands, temporary
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Wednesday, May 23rd, 2012
Julie Marshall at CK Science is currently looking for a QA Auditor to join the Quality Auditing team of a successful pharmaceutical company based in Sussex.
This QA Auditor role is a full-time, temporary role. If successful, you will be joining a global company and in return there is an attractive salary, coupled with career progression opportunities.
To be considered for this Quality Assurance Auditor position, you will have the following qualifications, skills and experience:
- Experience in performing and maintaining compliance audits in line with Regulatory and QMS requirements
- Experience in leading Audits, including scheduling, planning, executing, reporting and CAPA management
- A degree (or equivalent) in an appropriate discipline or related experience
- Knowledge of GMP regulations and in-depth knowledge of Quality Management Systems
- Certified Auditor/Internal/External
- Experience within a quality function or from a quality based role within manufacturing
How to apply:
Please contact Julie for more details.
Click here to apply online now.
For more information regarding this QA Auditor position, please contact Julie Marshall at CK Science on 01438 723500 or email jmarshall@ckscience.co.uk. Please quote reference ST24342 in all correspondence.
Tags: auditing, auditing jobs, auditing jobs sussex, auditor, auditor jobs, auditors jobs, jobs in sussex, Julie Marshall., pharmaceutical company, QA, QA Auditor Job in Sussex, QA jobs, qa jobs sussex, quality assurance, quality assurance jobs, quality assurance jobs uk, quality auditor jobs, quality auditor jobs sussex, sussex
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Monday, May 21st, 2012
Naynesh Mistry at CK Science is currently recruiting for a Product Compliance Head to join a global pharmaceutical company at their site based in the East Midlands on a permanent basis.
Product Compliance Head Job Description
As Product Compliance Head, you will manage the compliance across the 3 production units, ensuring that all aspects of the handling, manufacturing and distribution of pharmaceutical products comply with the requirements of the Quality Manual and Policies and meet all relevant cGMP regulatory and legislative requirements
The purpose of this Product Compliance Head position is to provide technical leadership for the site in all product quality compliance related matters and ensure operational business comply with cGMP legal and regulatory requirements.
Key responsibilities of this Product Compliance Head job will include:
- Ensure that all aspects of the handling, manufacturing and distribution of pharmaceutical products at the site comply with the requirements of the Pharma Corporate Quality Manual and Policies and meet all relevant cGMP regulatory and legislative requirements.
- Ensure that the local Quality System and Standard Operating Procedures are in place and that compliance with cGMP
- Ensure that a high quality of products is achieved through qualification and validation based upon quality risk analysis.
- Ensure that the QA department maintains an innovative approach based on improvement, implementation of best practice.
- Provide leadership, direction and support to the people within the QA Compliance area and ensure that they are qualified, achieve a high level of competence, are motivated and carry out their duties in a safe manner.
- Maintain current knowledge of local and international regulatory and legislative requirements and trends to ensure that expert advice and appropriate technical support on product quality related matters is provided to the whole site.
- Ensure that all components, drug product containers, closures, in process materials, packaging material, labelling and drug products are released in accordance with the registered specifications.
- Manage complaints, recalls, counterfeits and product tampering according to the company Corporate Quality Manual.
To be considered for this Product Compliance Head position, you will have the following qualifications, skills and experience:
- A degree in Sciences or equivalent
- Experience in Quality Assurance and Quality Control and/or in manufacturing environment within the Pharmaceutical industry.
- Previous experience in API manufacture and ICH guidelines are preferred, however experience within secondary pharmaceutical manufacture will also be considered if you show the technical and managerial skills required for this role.
- Sound knowledge of pharmaceutical regulatory requirements and be familiar with international guidelines, including FDA and MHRA.
Please contact Naynesh for more details.
How to apply:
Please click here to apply online now.
For more information regarding this Product Compliance Head position, please contact Naynesh Mistry at CK Science on 0114 283 9956 or email nmistry@ckscience.co.uk. Please quote reference SH24328 in all correspondence.
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Tags: compliance jobs, compliance jobs uk, compliance manager jobs, head of compliance jobs, Jobs, laboratory jobs, pharmaceutical company, Pharmaceutical industry, Product Compliance Head Job in East Midlands, QA, Recruitment, Regulatory, regulatory compliance jobs, science jobs, science jobs east midlands, science jobs uk, senior compliance jobs
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Friday, October 7th, 2011
Jim Gleeson at CK Science is currently recruiting for a Director of Quality Assurance to join a successful molecular diagnostics company based in the North West, UK.
The role:
As Director of Quality Assurance, you will oversee all Quality Assurance activities for the manufacture of in-vitro diagnostics. Further responsibilities will include:
- Management of the company’s Quality System
- Close interaction with senior management and international regulatory authorities
- Ensuring the highest levels of compliance with all applicable standards and regulations
- Mentoring and development of staff across QA, QC and Compliance
- Selection of methods, techniques and evaluation criteria in order to obtain robust results
The ideal candidate:
- Jim is looking for candidates with the following skills, experience and qualifications:
- Extensive GMP QA management experience, ideally within the diagnostics / medical device arena
- Experience of hosting and managing FDA and other regulatory inspections (ISO 13485 would be particularly useful)
- A background in ISO 13485 management would be advantageous
- Excellent communication skills
How to apply:
For more information or to apply for this Director of Quality Assurance position, please contact Jim Gleeson on 01438 870027 or email jgleeson@ckclinical.co.uk. Please quote reference CL22921 in all correspondence.
Tags: CK Science, ck science jobs, ck science recruitment, diagnostics, Director, director of quality assurance, Director of Quality Assurance Job in North West, GMP, IVD, Jim Gleeson, jobs in quality assurance, QA, quality assurance, quality assurance jobs, quality assurance jobs in north west, uk
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Wednesday, August 31st, 2011
Naynesh Mistry at CK Science is recruiting for a QA Technologist to join a Food Manufacturer at their site in West Yorkshire on a permanent basis.
Responsibilities:
- Responsible for gathering food specification information both internally and externally
- Interpretating/inputting the data so it matches the requirements for customer specifications
- Updating and maintaining all finished product specifications
- Creating pack copy for technical aspects of product artwork and labels
- Liaising with ingredient and packaging suppliers
- Maintaining technical information systems
You:
The successful candidate for this QA Technologist job will be educated to degree level, or equivalent in a food related subject with experience of BRC or ISO9000 auditing and have Quality Assurance experience including HACCP and internal auditing.
How to apply:
For more information or to apply for this QA Technologist position, please contact Naynesh at CK Science on 0114 283 9956 or email nmistry@c kscience.co.uk. Please quote reference SH22603 in all correspondence.
Tags: BRC, food industry jobs, food labelling, food science, HACCP, ingredient specifications., internal audition, QA, qa technologist, qa technologist job in west yorkshire, qa technologist jobs, qa technologist jobs west Yorkshire, science jobs
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Thursday, August 11th, 2011
Graeme Pallas at CK Science is currently looking to recruit a Senior Quality Technical Officer to join a food company located in North East England on initially a 6 month temporary basis.
Responsibilities:
The successful applicant will be responsible for a small quality team ensuring that food products meet set quality standards. They will also attend key meetings and provide advice on quality assurance.
Skills required:
Good communication skills are required along with a demonstrable record as a leader. Ideally, you will be familiar with Good Manufacturing Practice (GMP).
How to apply:
For more information or to apply for this Senior Quality Technical Officer role please contact Graeme Pallas on 0191 384 9805 or email gpallas@ckscience.co.uk. Please quote reference DH22522 in all correspondence.
Tags: food jobs, GMP, QA, quality assurance, quality manager, quality officer, quality technical officer, science jobs uk, Science recruitment uk, scientific jobs uk, scientific recruitment, scientific recruitment agencies uk, scientific recruitment uk, technical coordinator, Technical Manager, technical officer
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