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161 Pharmaceutical Jobs found


Sponsored

Senior QA- Pharmaceutical/GMP

Jobs in Manchester,Greater Manchester,North West England

Russell Taylor Group Ltd Jobs
 Permanent
 Posted about : 15 days ago

Role: Senior QA- Pharmaceutical/gmp
Location: Manchester
Salary: Competitive
Type: Permanent
Start: Immediately

Our Client, a well-known Pharmaceutical manufacturing company are looking to bring in an experienced Senior QA candidate who has vast experience in the QMS, documentation and have worked in the GMP Pharmaceutical industry.

The Role:

  • Assisting with QMS implementation and upkeep by:
  • Raising CAPA / Deviations
  • Implementing Change Controls
  • Assisting with audits / internal
  • Implementing a new paperless system
  • Managing and mentoring more junior staff members

The Person:

  • 5+ years' experience in QA in a pharmaceutical setting (essential)
  • Must have experience in tablets/capsules
  • Significant CAPA, OOs, Deviation/s, Change Control/s, Complaints, and internal auditing experience within an GMP - MHRA/Pharmaceutical accredited setting ONLY.
  • Strong Excel skills needed to assist with the new paperless system
  • Leadership skills needed/ previous training - supervising/ mentoring experience.

Important Information: We endeavour to process your personal data in a fair and transparent manner. In applying for this role, Russell Taylor will be acting within your interest and will contact you in relation to the role, either by email, phone or text message. For more information see our Privacy Policy h t t p s : / / w w w . r u s s e l l - t a y l o r . c o . u k / p r i v a c y - p o l i c y on our website. It is important you are aware of your individual rights and the provisions the company has put in place to protect your data. If you would like further information on the policy or the GDPR please contact us on h r @ r u s s e l l - t a y l o r . c o . u k

Sponsored

QC Lab Manager, Pharmaceutical

Jobs in Bolton,Greater Manchester,North West England

Russell Taylor Group Ltd Jobs
 Permanent
 Posted about : 16 days ago

Role: QC Lab Manager, Pharmaceutical

Location: North West, UK

Salary: Negotiable

Russell Taylor Group has an excellent opportunity for a QC Lab Manager to join a leading Pharmaceutical Company based in the North West. You will ensure that batches are tested in a timely manner to meet business needs and in compliance with GMP. Perform and supervise validation activities in line with ICH guidelines. Provide leadership and support to all areas of the laboratory, raw materials, stability, IPC, and documentation compliance.

Role:

  • Management of finished product, stability and raw material testing to ensure results availability in line with business targets and testing performed to GMP standards.
  • Support with analytical validation activities
  • Raising any/HOQ/QP of any issues that may impact on the business
  • Liaising with Planning/Packaging Manager to ensure testing schedules meet packaging timeline requirements
  • Ensuring all standard, reagents and consumables are available for testing
  • Ensuring all paperwork is issued on time to meet testing schedule requirements
  • Liaising with raw material/stability analysts to efficiently test products.
  • Reviewing testing as defined by second check process.
  • Progressing analytical investigations arising from OOS/OOT/OOE
  • To be competent in the preparation and execution of test method and laboratory equipment validation documentation.
  • Support the reviewing of laboratory documentation to ensure smooth running of the laboratory.
  • Undertake project work as directed.
  • Competent in wet chemistry and analytical techniques, including FTIR, UV VIS, HPLC and Karl Fischer.
  • Generate QC deviation reports and complete timely and effective investigations of GMP non-conformance in the laboratory.
  • Competent in principles and application of data integrity and ensuring the QC team comply with data integrity requirements.
  • Perform effective trouble shooting following equipment breakdown
  • Accurately work to a consistently high standard
  • Maintain good housekeeping standards
  • Develop and maintain good working relationships within and outside the department
  • Implementation of KPI's to monitor the team's activities and resources and improve efficiency.Key Skills
  • QC Analytical Skills - specifically solid dose
  • Understanding of analytical validation and instrument qualification
  • Experience of managing a small team
  • Attention to detail
  • Effective time management skills with the ability to prioritise effectively.
  • Good team player
  • Experience in problem solving

Person:

  • A minimum of 10 years previous experience within a pharmaceutical environment.
  • A minimum of 5 years previous experience of supervising/leading a small team
  • A relevant scientific degree
  • Experience in Laboratory instrument qualification
  • Experience in analytical method development/validation and cleaning validation
  • Experience in solid dose testing
  • Knowledge of GMP laboratory requirements

Important Information: We endeavour to process your personal data in a fair and transparent manner. In applying for this role, Russell Taylor will be acting within your interest and will contact you in relation to the role, either by email, phone or text message. For more information see our Privacy Policy h t t p s : / / w w w . r u s s e l l - t a y l o r . c o . u k / p r i v a c y - p o l i c y on our website. It is important you are aware of your individual rights and the provisions the company has put in place to protect your data. If you would like further information on the policy or the GDPR please contact us on h r @ r u s s e l l - t a y l o r . c o . u k

External

International Sales Manager (Pharmaceutical/Tech Solutions)

Jobs in Lambeth,Greater London,London

£45,000 - £55,000 /Annum
 Permanent
 Posted about : 7 days ago

International Sales Manager (Pharmaceutical/Technical Solutions) £50,000 - £55,000 + Car + Bonus (80k OTE) + Company Benefits Home Based - UK Wide Travel Are you a Technical Sales Engineer with experience of selling into Pharma Manufacturers, R&D or Biotech looking for a senior level role where you can grow, develop and shape your own career and progress in a small, growing business? On offer is a role where you can develop a key client base, targeting pharma manufacturers where the environment is heavily regulated. You will be a major player and a key member of staff in the business where you will be presenting to senior level Directors and have a regular presence in your territory. This company are a small, specialist instrumentation company who supply, install, calibrate and service Electronic instrumentation for the life science industry. Their key clients are mainly in the pharmaceutical space. This role would suit a Technical Sales Engineer with experience of selling systems or equipment into Pharma Manufacturers, R&D, Biotech, Clinical Trials as well as 3PLs and Wholesalers looking for a senior level role where you can grow, develop and shape your own sales team in the future. THE ROLE The role combines new business development and the management and development of some existing accounts. The role reports to the Commercial Manager and will also work closely with the Commercial Director and the Service Managers. Ensure that the quarterly and annual sales targets are achieved Identify your customers' needs, goals and challenges, and provide solutions to these through the proper positioning of products, services, knowledge and expertise; inform and influence customers Know and be known by your customers; maintain a regular presence within your territory Follow-up on leads, close action items and customer requests completely and in a timely fashion Secure targeted meetings to identify and advance opportunities with your customers Identify and map the key stakeholders and decision makers around projects and opportunities Create and deliver presentations; coordinating appropriate resources for customer visits Manage forecasting and pipeline by utilizing the CRM to manage, track, and report on all sales activities; provide, accurate, detailed forecastsTHE PERSON Technical Sales background Experience of selling into the pharma industry Pharma, R&D, Manufacturing, Biotech, Clinical, Medical, sales, Business Development, London, Life Science, Development, Engineering, If you're interested in this role, click 'apply now' to forward an up-to-date copy of your CV, or call us now. If this job isn't quite right for you but you are looking for a new position, please contact us for a confidential discussion on your career. Ernest Gordon Recruitment Limited acts as an employment agency for permanent recruitment and employment business for the supply of temporary workers. By applying for this job, you accept the T&C's, Privacy Policy and Disclaimers which can be found at our website

External

International Sales Manager (Pharmaceutical/Tech Solutions)

Jobs in Ridgacre,Birmingham,West Midlands

£50,000 - £55,000 /Annum
 Permanent
 Posted about : 7 days ago

International Sales Manager (Pharmaceutical/Technical Solutions) £50,000 - £55,000 + Car + Bonus (80k OTE) + Company Benefits Home Based - UK Wide Travel Are you a Technical Sales Engineer with experience of selling into Pharma Manufacturers, R&D or Biotech looking for a senior level role where you can grow, develop and shape your own career and progress in a small, growing business? On offer is a role where you can develop a key client base, targeting pharma manufacturers where the environment is heavily regulated. You will be a major player and a key member of staff in the business where you will be presenting to senior level Directors and have a regular presence in your territory. This company are a small, specialist instrumentation company who supply, install, calibrate and service Electronic instrumentation for the life science industry. Their key clients are mainly in the pharmaceutical space. This role would suit a Technical Sales Engineer with experience of selling systems or equipment into Pharma Manufacturers, R&D, Biotech, Clinical Trials as well as 3PLs and Wholesalers looking for a senior level role where you can grow, develop and shape your own sales team in the future. THE ROLE The role combines new business development and the management and development of some existing accounts. The role reports to the Commercial Manager and will also work closely with the Commercial Director and the Service Managers. Ensure that the quarterly and annual sales targets are achieved Identify your customers' needs, goals and challenges, and provide solutions to these through the proper positioning of products, services, knowledge and expertise; inform and influence customers Know and be known by your customers; maintain a regular presence within your territory Follow-up on leads, close action items and customer requests completely and in a timely fashion Secure targeted meetings to identify and advance opportunities with your customers Identify and map the key stakeholders and decision makers around projects and opportunities Create and deliver presentations; coordinating appropriate resources for customer visits Manage forecasting and pipeline by utilizing the CRM to manage, track, and report on all sales activities; provide, accurate, detailed forecastsTHE PERSON Technical Sales background Experience of selling into the pharma industry Pharma, R&D, Manufacturing, Biotech, Clinical, Medical, sales, Business Development, London, Life Science, Development, Engineering, If you're interested in this role, click 'apply now' to forward an up-to-date copy of your CV, or call us now. If this job isn't quite right for you but you are looking for a new position, please contact us for a confidential discussion on your career. Ernest Gordon Recruitment Limited acts as an employment agency for permanent recruitment and employment business for the supply of temporary workers. By applying for this job, you accept the T&C's, Privacy Policy and Disclaimers which can be found at our website

External

QA Officer - Pharmaceuticals

Jobs in Skipton,Craven,North Yorkshire,Yorkshire and the Humber

£22,000 - £26,000 /Annum
 Permanent
 Posted about : 7 days ago

An established pharmaceutical company in Yorkshire are currently looking to recruit QA Officers to join their team at a busy pharmaceutical manufacturing facility As a QA Officer you will be experienced in all aspects of Pharmaceutical Quality Assurance supporting key elements of the QMS including change controls, deviations, CAPAs and customer complaints. Responsibilities Writing, reviewing and distributing Quality System Documents Supporting master batch documentation (BMR/BPR/GPS) review and issuance Providing line clearance for the dispensing of raw materials, packaging materials and finished product Performing In-Process Quality checks at various stages of the manufacturing, filling and packaging process Ensuring adherence to SOPs in the warehousing, engineering and manufacturing departmentsRequired Skills A Degree within a Life Science related field or equivalent industrial experience Demonstrable experience working within QA/QC in the pharmaceutical industry Demonstrable understanding of current regulatory requirements for the manufacture of licenced medicinal products Proven knowledge and understanding of GMP, GDP and EU and UK pharmaceutical regulations Flexibility for working shifts including the potential for nights and weekendsThe requirement for this QA Officer is urgent with a view to starting as soon as possible so please apply now or contact Gareth Gooley at Science Solutions Recruitment for more information

Sponsored

QP-Batch Release (Pharma)

Jobs in Manchester,Greater Manchester,North West England

Russell Taylor Group Ltd Jobs
 Permanent
 Posted about : 15 days ago

Role:- QP (Batch release- pharmaceutical) Location:- Manchester
Salary:- Highly competitive

A fantastic opportunity for an experienced qualified QP to join a growing pharmaceutical manufacturing company in North West England. You must have a demonstrable record of experience in a similar role, an excellent understanding of the pharmaceutical market and strong team management experience.

Responsibilities

  • Act as releasing QP for the site to EU Directive 2001/83/EC & Eurdralex Volume 4 Annex 16
  • Support the Director of Quality in the development and implementation of the Quality department strategy.
  • Contribute and support to inspections and audits (customer & regulatory)
  • Maintain an awareness of new and anticipated legislation that may impact the business and be able to communicate these changes to senior management and any other individuals of the business if needed.
  • Review & approve quality and technical documents
  • Ensure that investigations are dealt with suitably and in a timely manner (this will include errors, complaints, failures, or AE both internally and externally)
  • Ensure that the quality department improve or if not meet the budget, costing, volume and KPI targets of the business.
  • Support and give guidance to trainee QPS of the business and support the wider quality team if required.
  • Undertake any other duties for either the quality team or other departments within the business when requested by the line manager

The Person

  • BSc in either Pharmacy, Pharmaceutical Science, or a Chemistry related degree
  • Qualified QP who has worked to EC/2001/83- with previous industry experience in a similar role at similar level
  • Excellent understanding of pharmaceutical markets
  • Understanding of processes used in the manufacturing and packaging of oral solid dose products
  • Experience of team management and leadership
  • Able to communicate at an exceptionally high standard (verbal and written)
  • Strategic thinker
  • Customer focused and commercially knowledgeable

Important Information: We endeavour to process your personal data in a fair and transparent manner. In applying for this role, Russell Taylor will be acting within your interest and will contact you in relation to the role, either by email, phone or text message. For more information see our Privacy Policy h t t p s : / / w w w . r u s s e l l - t a y l o r . c o . u k / p r i v a c y - p o l i c y on our website. It is important you are aware of your individual rights and the provisions the company has put in place to protect your data. If you would like further information on the policy or the GDPR please contact us on h r @ r u s s e l l - t a y l o r . c o . u k

External

Production Operator 8am-4pm Mon-Friday

Jobs in Chester,Cheshire West and Chester,Cheshire,North West England

 Permanent
 Posted about : 7 days ago

Production Operator, Pharmaceutical Manufacturing, Deeside. 8am-4pm Monday to Friday - Entry level salary of £17500 - rising to £18k once trained We are looking for candidates from ideally a small GMP production or packaging background who can be flexible and enjoy a variety of tasks within a multi-disciplined, growing production department Outstanding organisation who have experienced tremendous growth and an increased presence in the pharmaceutical industry in the last 3 years. This is a chance to join their production team in a growing pharmaceutical operation We are ideally looking for Operators who have a lab background as this is lab-based/cleanroom production role;Responsibilities of the Cleanroom Production Operator Include; Laboratory based/cleanroom production of pharmaceutical products To set up the production area in preparation for production operations in accordance with GMP, including routine checking and testing of equipment and environmental conditions. Completing batch processing documents using simple mathematical calculations.Desirables; Ideally the cleanroom Production Operator will have experience in the Laboratory & as an operator Understanding and following Good Manufacturing Practice (GMP) and maintaining high housekeeping standards, including high level cleans Enthusiasm and drive to succeed, develop and progress through the manufacturing department. Ability to follow instructions with accuracy Excellent verbal and written communication skills Self-motivated and proactive Team player who enjoys and works well within a small team A flexible attitude and commitment to work extended hours in peak periods. Reconciliation skillsPlease apply now to be considered immediately

External

QC Manager

Jobs in Salisbury,Wiltshire,South West England

£44,000 - £54,000 /Annum
 Permanent
 Posted about : 7 days ago

RHL has a long-standing relationship with a leading UK based biopharma manufacturing company, which focus on unique life-saving vaccination products. Based on ongoing expansion they are recruiting for a QC Microbiology Manager to join them to support the new Director of Quality in taking the business forward into their next phase of growth. This is a fantastic opportunity for a strong Manager to closely collaborate with the Leadership team to impact upon quality of life across a number of specialist pharmaceutical products. On top of that is a generous base salary and a very generous package to include 38 days holiday. Since being established in 2015, the company has doubled in size and is now looking for someone to lead the Microbiology Department to successfully deliver quality products on time in full. This role will provide Line Management for 4 area managers supervising established teams within the microbiology department. The overall team equates to approximately 30 quality professionals. You will be joining the Quality Division, who are responsible for ensuring that the manufactured product is safe, efficacious, and fit for patient use as a pharmaceutical material. Key responsibilities Lead the QC Microbiology Group and ensure all quality activities are performed in compliance with regulations and other requirements including: The Rules & Guidance for Pharmaceutical Manufacturers' and Distributors, cGMP guidance, and other regulations governing activities; Lead projects and deliver required outcomes in their own specialist area; Lead, motivate, coach, mentor and manage the performance and output of the Microbiology Team (including direct managerial reports) and ensure that all team objectives are met in agreed timescales; Maintain and develop the local standard operating procedures to secure effective working practices as well as compliance with relevant national, European and US legislation; Monitor the performance of the systems under area of responsibility using KPIs and report to management; Develop and implement an ongoing Quality Improvement Plan related to the systems under area of responsibility; Lead the development and implementation of an ongoing Health & Safety Plan for the team to secure the right level of performance, highlight failures and make recommendations for solutions; In line with overall responsibilities, perform additional tasks assigned by the line manager. You will need Have a degree, or equivalent, in an appropriate scientific discipline; Strong Microbiology experience; Demonstrable experience with managing and leading trained industry professionals; Experience of managing and operating quality systems for compliance, to regulatory requirements; Experience with dealing with internal customers, negotiating and agreeing work programmes, reporting progress and dealing with issues to ensure delivery and customer satisfaction; Substantial practical experience within a GMP environment, particularly in the context of biologics and steriles manufacture; Knowledge and experience of aseptic manufacture; Knowledge of EU/US pharmaceutical regulatory requirements for biologics and sterile products.Please apply to Kosh Santra below - (url removed) Recruitment Holdings Ltd (RHL) acts as an employment agency and employment business

Sponsored

Junior Regulatory Affairs (Pharma/Med Device)

Jobs in Manchester,Greater Manchester,North West England

Russell Taylor Group Ltd Jobs
 Permanent
 Posted about : 14 days ago

Role: - Junior Regulatory Affairs

Salary: - Competitive

Location: - Manchester

Russell-Taylor Group have a fantastic opportunity for a junior regulatory affairs associate/officer to join a rapidly expanding pharmaceutical manufacturer/distributor in the North West. If you have 1-2 years RA experience in a pharmaceutical environment, then please apply within.

Responsibilities

  • Support the Head of Regulatory services for existing product portfolio and future product opportunities for medicinal products and medical devices- submissions and retrieval of analytical/manufacturing process data to support MAA
  • Assist the PV team when required in relation to medical information queries, upload of approved product information to the eMC & ensure that additional risk minimisation measures required for a product are implemented (e.g.- additional follow up)
  • Support audit preparation activities for department and of external vendors
  • Assist in performing gap analysis
  • Validate that product packaging is updated and maintained in accordance with product licences & international territories which may include the review of artwork for product packaging.
  • Involvement in regulatory team meetings and manage assigned tasks with regular updates to the team
  • Ensure that planning, preparing, tracking, and storing submissions to regulatory agencies are regularly updated and used.
  • Maintenance of new & existing Marketing Authorisations registered via National and potential Material requirement planning.
  • Communicate efficiently with key stakeholders both internally and externally- building a good relationship with them!
  • Ensure familiarity with the company's product range and keep up to date with the company's regulatory standards and legislation for both UK and EU. As well as ensuring quality standards are consistently met and submissions are made accordingly.
  • For both national and mutual recognition procedures prepare, compile, and submit a range of regulatory applications
  • Liaise with various departments including Company Engineers and the Procurement Team to create, maintain and implement approved artwork drafts
  • Report to the QPPV any updates on regulatory applications
  • Liaise with the finance department with arrange payment fees to MHRA and other authorities when required
  • Review and update SOPS to ensure they comply with applicable legislation with the UK & EU
  • Actively seek to minimize risks to the business, Manage and alert risks via the Regulatory and Quality Manager

The Person

  • BSc in a life science, healthcare, or pharmaceutical discipline
  • Knowledge of national and MRP in the UK/EU
  • Experience within RA within either Pharmaceutical or Medical Device
  • Excellent understanding of analytical & manufacturing sciences in the pharma industry
  • Experience or preparing and submitting post-marketing regulatory applications to the MHRA (variations, renewals, post-marketing commitment submissions, PSURs)
  • Experience of writing and updated product information documents to an excellent standard. This will include development of labelling & leaflet artworks.

Important Information: We endeavour to process your personal data in a fair and transparent manner. In applying for this role, Russell Taylor will be acting within your interest and will contact you in relation to the role, either by email, phone or text message. For more information see our Privacy Policy h t t p s : / / w w w . r u s s e l l - t a y l o r . c o . u k / p r i v a c y - p o l i c y on our website. It is important you are aware of your individual rights and the provisions the company has put in place to protect your data. If you would like further information on the policy or the GDPR please contact us on h r @ r u s s e l l - t a y l o r . c o . u k

External

Sales Account Manager

Jobs in Stanwell Moor,Spelthorne,Surrey,South East England

£30,000 - £35,000 /Annum
 Permanent
 Posted about : 7 days ago

Sales Account Manager Location: Staines-upon-Thames Hours: Full Time (Mon-Fri) Salary: £30,000 - £35,000 per annum, depending on experience Our client is a small, established, family-owned pharmaceutical company, focused on the development, marketing and export of generic medicines and raw materials. Customers include pharmacies, hospitals, pharmaceutical wholesalers, relief organisations and government agencies worldwide. They are now looking to recruit an experienced sales account manager to join their growing team. From day one in this role, you will have a high-level of responsibility with a broad focus and opportunity to deliver real impact. Duties Include: Managing customer enquiries from quote, to order, and invoice. Establishing productive, professional relationships with key personnel in assigned client accounts. Developing and implementing a new account management strategy to generate significant and sustainable revenue. Developing and implementing a strategy for new business opportunities. Sourcing products and negotiating commercial terms with suppliers and contract manufacturers. Maintaining thorough records of all sales & purchasing activity. The Ideal Candidate: Minimum of 3 years’ experience in a sales or business development role, within either the healthcare or pharmaceutical industry. Native English language skills, with an ability to communicate clearly and idiomatically. Relevant university BA/BS degree. Excellent ability using Microsoft Excel, and Sage accounting software. Proactive, independent worker who is highly organised and interested in the difference they can make through their individual contribution to expand the business. Happy and able to commute to our office by Staines-upon-Thames, near Heathrow. If you’re the ideal candidate our client is looking for, please send your Covering Letter and CV by clicking the APPLY button Keywords:  Sales, Account Manager, Business Development, Pharmaceuticals, Healthcare, Export, Pharma, Generics

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