Tom Evans

Account Consultant

I started my QCS Staffing career in 2019, having joined the business with 2 years of prior recruitment experience. Currently working as an Account Consultant, I help in managing some of our most valued clients, as well as sourcing exceptional candidates.

Typical pharma/biotech jobs I recruit for are in engineering, quality, and manufacturing. Outside of work I enjoy sport & exercise, following Watford FC, and spending time in Berkhamsted pubs!

View our latest jobs

Posted 13 days ago

Process Engineer

ContractLimerick, County Limerick, Ireland

Process Engineer - Ireland, Limerick - 12 Month ContractIreland is a hive of activity for the Life Sciences Sector at present with global players setting up new and expanding existing manufacturing facilities all over the World. An exciting opportunity has arisen to work for a global pharmaceutical organisation on a major expansion project based in the picturesque Limerick. What you'll do: Generation User Requirement Specification (URS) for assigned systems.Reviews and approves Basis of Design (BOD) and detail design of assigned systems i.e. PFDs, P&IDs, etc.Ensures procurement packages (bill of materials (BOM), datasheets, cutsheets etc) meet equipment specifications.Tracks HAZOP action items and ensures action items are incorporated into system design.Attends 30%, 60% and 90% model reviews ensuring systems meet operational, safety and ergonomic requirements.Reviews and approves system lifecycle documentation (FS. SDS, IO lists, etc) and ensures they meet requirements.Attends factory acceptance test (FAT) of associated equipment if required.Attends automation software bench FAT if required. What you'll need: Requires BS/BEng in Chemical, Process or Mechanical engineering with extensive related experience.Direct experience with biopharmaceutical process equipment is preferred.Relevant experience for education.Experience with design and commissioning within biopharmaceutical sector would be desirable.Experience with DeltaV would be desirable If this role is of interest to you, please apply now! #LI-TE1

Posted 13 days ago

Senior EHS Specialist

ContractDublin, County Dublin, Ireland

Senior EHS Specialist - Ireland, Dublin - 5 Months ContractDo you want to be involved with one of Dublin’s most exciting bio-pharmaceutical manufacturers?This is an opportunity to support both sustaining operations and new capital projects; with lots of opportunities to work with and learn about cutting-edge technologies, in addition to developing your own skills.  This is a truly exciting facility producing lifesaving biologics-based medicines.Responsibilities: SME support in General Safety and High Risk Work Programs.SME support in Environmental Programs (Air, water, waste).Provide safety support for new ongoing and new projectsParticipate in local safety teams, audits and inspections, incident investigations, and other safety programs as required.EHS representative for risk assessments, change management impact assessments, training delivery, and contractor management.EHS Assessment and auditing of EHS process and systems in line with Safety and Environment Standards. Requirements: Requires extensive experience in EHS, Engineering, or Operational experience in chemical, pharmaceutical, biochemical, petrochemical, or process related industry.In Depth Knowledge of Irish H&S and Environmental Legislation and regulationsHigh Risk Work program (Electrical safety, LOTO, Hot work, confined space etc) and Contractor Management experience beneficialAbility to maintain focus on key goals and priorities, but also analyse the detail to facilitate problem resolution and ensure project successProven record of success in the EHS sector.  If this role is of interest to you, please apply now!#LI-TE1

Posted 13 days ago

EHS Specialist

ContractCarlow, County Carlow, Ireland

EHS Specialist - Ireland, Carlow - 11 Months Initial ContractDo you want to be involved with exciting pharmaceutical projects? When it comes to the development and production of veterinary vaccines, our pharmaceutical client has the largest centre in the industry worldwide and is a Centre of Excellence; employing more than 1000 people. They are looking to add to their team and require an EHS Specialist. Essential Duties and Responsibilities for this role include, but are not limited to, the following: Develop and implement EHS programs to ensure compliance with local legislation, standards, and industry best practices. Assist operational departments in achieving and establishing compliance.Demonstrate leadership and a strong desire to protect employees, our community, and the environment in this world-class facility – leading with a ’safety first’ mindset.Prepare reports to site, divisional and/or corporate management and regulatory agencies.Evaluate all EHS applicable requirements for any new projects and processes (along with other site departments where necessary) as well as changes in the existing processes and installation. Desirable Experience: Technical Bachelor Degree in Environmental Health & Safety or Technical Bachelor’s Degree (Science/Engineering).Post-grad EHS qualification would be a plus.Extensive EHS experience in Pharmaceutical, or other highly regulated industry.Proven track record of success in the environmental health and safety sector. If this role is of interest to you, please apply now!#LI-TE1

Posted 13 days ago

Senior QA Specialist

ContractClonmel, County Tipperary, Ireland

Senior Quality Assurance Specialist - Ireland, Clonmel - 11 Month ContractDo you want to be involved with exciting pharmaceutical projects? When it comes to the development and production of veterinary vaccines, our pharmaceutical client has the largest centre in the industry worldwide and is a Centre of Excellence; employing more than 1000 people. They are looking to add to their team and require a Senior Quality Assurance Specialist. Essential Duties and Responsibilities for this role include, but are not limited to, the following: Lead the QA review and approval process for Change Controls, Deviations/CAPAs, SOPs, and related documentation, ensuring full compliance with GMP and site-specific requirements.Manage QA operational duties related to product disposition, ensuring timely and compliant decision-making.Monitor and evaluate new regulatory guidance and industry best practices, assessing their impact on quality systems and driving necessary updates.Assist in developing and maintaining QA policies, SOPs, and reports that support site operations and compliance. Desirable Experience: Degree in Science, Quality, or a related Technical field.Requires extensive experience in Quality Assurance, Quality Control, or Technical Operations within FDA/EMEA regulated environments.Strong written and verbal communication skills, capable of clearly articulating complex quality issues. If this role is of interest to you, please apply now!#LI-TE1

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