ALMAC GROUP

Responsibility

• production Technician
• undertake complex process development, qualification, and validation works related to equipment installation, operational qualification and validation experiments
• accurately record and complete technical information and GMP documentation during production operations associated with pharmaceutical development, manufacturing and packaging operations
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• location: Craigavon
• hours: Rotating shift Mon - Fri
• undertake complex process development, qualification, and validation experiments as well as routine GMP operations, activities related to equipment installation, operational qualification and validation experiments
• operate process equipment according to internal procedures controlling process parameters with limits as defined within SOPs, Protocols and Master Batch Records and where required become the subject matter expert for specific pieces of equipment or processes, including equipment set-up, optimum operation, strip down and cleaning, product changeover
• communicate and interact with staff from other departments including Technical Support, Quality Control, Quality Compliance, Technical Quality, Engineering & Facilities to ensure that operations are planned and executed in an efficient manner
• business Unit: Almac Pharma Services
• provide support to Production Operators/ Senior Operators, Supervisors and Technical Staff by assisting in process development, qualification and validation experiments as well as routine GMP operations
• ensure GMP standards are maintained at all stages of manufacture in line with internal procedures and regulatory requirements. Report any incidents to management that have the potential to impact the quality of the process/ equipment or product
• open To: Internal and External Applicants
• refer to the attached Job Descriptions and Person Specification for each role for full details and further information. Please make sure your CV clearly demonstrates how you meet the criteria required before submitting your application

Requirements

• please submit your CV via the online portal ensuring you clearly detail your qualifications and relevant experience
• the expert services we provide supports the provision of medicines and treatments to patients around the world
• the role of a Production Technician is to provide technical expertise within work centres ranging from manufacturing, primary and secondary packaging
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• at this point, we are seeking to establish a pool of suitable candidates only for current and future vacancies. Please note you are not actively applying to an open position at this time
• the Production Technician must also ensure operational compliance with Quality Management Systems , and adherence to Health and Safety policies
• please also note CVs will be assessed on an ongoing basis and you may be contacted depending on the roles available, your skill set and business requirements
• with a wealth of knowledge and experience, Almac Pharma Services have been manufacturing medicines in tablet, capsule and powder form for over 50 years
• we have opportunities available to join us as a Production Technician in our Packaging and Manufacturing teams
• we also pack commercial drug products into bottles, blisters and sachets and provide specialised packaging solutions for medical kits, vials and syringes
• the principal function of the role is to ensure the efficient and effective running of technical operations, in accordance with associated protocols & batch documentation whilst maintaining schedule adherence

Earnings for position production technician

Responsibility

• as part of a busy team within a rapidly growing organisation, operating within a challenging industry you will benefit from the numerous personal and professional developmental opportunities available throughout the Almac group

Requirements

• BSc in Chemistry
• degree level qualification in Analytical / Chemistry, or closely related discipline
• applicant criteria for this role can be found in the attached Job Descriptions and Person Specification
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• postgraduate level qualification in a related discipline
• demonstrated hands on experience in one or more of the following MS techniques in an industrial or academic environment; LC-MSn, GC-MSn
• applicants must fully show, by way of example, how they meet each aspect of the essential criteria for shortlisting purposes
• phD level qualification in Mass Spectrometry
• experience of structure elucidation and quantitative analysis using MS
• previous relevant industrial experience in a GMP/GLP environment
• desirable Criteria may be applied if a large pool of applicants exist
• theoretical knowledge of multiple laboratory techniques
• experience of MS analysis of peptides and proteins as well as small molecules
• experience of method Validation

Earnings for position chemist

Responsibility

• commercial Relationship Manager
• location: Craigavon
• hours: 37.5 Hours per week
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• business Unit: Pharma Services
• open To: Internal & External Applicants

Requirements

• bachelor’s degree qualification
• previous experience working within customer relationship or project management role OR Previous experience within the Pharmaceutical industry
• bachelors degree qualification in a Life Sciences, Engineering or Business related discipline
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• previous line management experience

Earnings for position commercial manager

Responsibility

• business Systems Team Leader
• location: Craigavon
• hours: 37.5 Hours per week
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• hours: 37.5 hours per week
• business Unit: Pharma Services
• open To: Internal & External Applicants
• open To: Internal and External Applicants
• to manage the progress of Analytical work to GMP requirements and ensure that project schedules are met and that the work is carried out efficiently and accurately, providing regular updates to their Head of Departmental
• coordinating people and activities across multiple functional areas particularly with Sales, Marketing, Finance, and operational business functions

Requirements

• essential Criteria
• postgraduate level qualification in a related discipline
• stability study design and testing
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• HPLC method Development
• MSc/PhD in a Chemistry or Life Science with a significant chemistry component
• experience working within an established Quality System within a Pharmaceutical Industry
• HPLC method Validation
• previous experience of analytical development for sterile pharmaceuticals
• experience in leading a team of quality professionals
• previous experience of implementing major laboratory change projects e.g. implementing LIMS software
• dissolution Method Development
• experience of solid oral dosage forms in development scale including clinical supply, and commercial scale manufacture
• dissolution Method Validation
• be trained as a Six Sigma greenbelt or above
• knowledge on Root Cause Analysis technique
• significant experience of supervising and cGMP laboratory activities and staff
• proven ability to manage direct reports and deal with people management challenges
• desirable Criteria
• A thorough understanding of the pharmaceutical drug development process, and experience preparing regulatory CMC dossier sections
• reward
• degree in a science, life science or technical discipline or closely related field OR Significant relevant experience and knowledge will be considered in lieu of degree
• experience of using statistical data analysis techniques and designing statistically relevant experiments
• A bachelor’s degree in a pharmaceutical discipline
• proven ability to successfully lead business improvement projects using recognised process improvement techniques
• root Cause Analysis Training
• proven ability to work effectively on own their initiative and effectively contribute, and lead within a team environment
• experience of other pharmaceutical dosage forms
• proven ability to manage multiple complex activities within a concurrent timeframe

Trade

• loading and Stocking
• Loading and Stocking

Responsibility

• friday
• location: Based at our state-of-the-art custom designed facilities in Craigavon
• hours: 37.5 hours per week
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• hours: 37.5 hours per week on our flexi hours Monday
• the expert services we provide supports the provision of medicines and treatments to patients around the world
• about You

Requirements

• 3 x A-Level at Grade C or above
• administrator, Quality, Pharmaceutical, FMCG, Food industry, IT, customer service, specification, traceability, documentation, regulated industry etc
• A-level qualification
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• additional Information
• previous experience within a quality system or manufacturing environment
• experience within a pharmaceutical / GxP environment
• management of electronic & physical documentation systems
• hybrid working options may be considered after completion of initial probation period
• apply Now
• apply online
• have eligibility to work in the UK OR possess a valid work permit that will allow you to take up full time employment in the UK
• please ensure your CV clearly outlines how you meet criteria for this role
• refer to the job description attached to this advert for full details of the essential and desirable criteria required
• A fantastic salary and benefits package is available, including annual bonus for all, generous holiday allowance, healthcare reimbursement scheme, and a rewarding role where the work you do will ultimately be contributing to the advancement of human health
• all applicants must have eligibility to work in the UK OR possess a valid work permit that will allow you to take up full time, permanent employment in the UK

Trade

• administrative Assistance
• Administrative Assistance