chemical processing technician

CORDENPHARMA

<div><h2 class="jobSectionHeader"><b>CORDENPHARMA</b><b> </b><b>IS A LEADING FULL-SERVICE CONTRACT DEVELOPMENT AND MANUFACTURING ORGANIZATION (CDMO) SPECIALIZING IN ACTIVE PHARMACEUTICAL INGREDIENTS (APIS), EXCIPIENTS, DRUG PRODUCTS (DPS), AND PACKAGING. WITH AROUND 3,000 EMPLOYEES WORLDWIDE, WE HELP PHARMACEUTICAL, AND BIOTECH COMPANIES MANUFACTURE MEDICINES WITH THE ULTIMATE GOAL OF IMPROVING PEOPLE&rsquo;S LIVES.</b></h2><h2 class="jobSectionHeader"><b>
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OUR NETWORK, SPANNING EUROPE AND THE U.S., PROVIDES FLEXIBLE AND SPECIALIZED SOLUTIONS ACROSS SIX TECHNOLOGY PLATFORMS: PEPTIDES, LIPIDS &amp; CARBOHYDRATES, INJECTABLES, HIGHLY POTENT &amp; ONCOLOGY, SMALL MOLECULES, AND OLIGONUCLEOTIDES. WE STRIVE FOR EXCELLENCE IN SUPPORTING THIS NETWORK AND ARE COMMITTED TO DELIVERING THE HIGHEST QUALITY PRODUCTS FOR PATIENT WELL-BEING.</b></h2><h2 class="jobSectionHeader"><b>
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OUR PEOPLE VISION</b></h2><h2 class="jobSectionHeader"><b>
WE STRIVE FOR EXCELLENCE. WE SHARE OUR PASSION. TOGETHER, WE MAKE A DIFFERENCE IN PATIENTS' LIVES.</b></h2><h2 class="jobSectionHeader"><b>
</b></h2><h2 class="jobSectionHeader"><b>
SUMMARY</b></h2><div>
Acts to drive and demonstrate the technology for the planning and execution of development and implementation of chemical processes. Ensures that the chemistry is sufficient to meet goals on process yields, throughputs, and QSHE requirements.</div><h2 class="jobSectionHeader"><b><br>
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ESSENTIAL DUTIES AND RESPONSIBILITIES</b></h2><div>
Include the following. Other duties may be assigned:</div><br>
<div></div><ul><li>
Familiarity with general TFF/ultra filtration setup, operation, and components</li><li>
Experience with lab and/or mid-large scale TFF/ultra filtration processing</li><li>
Knowledge of various types of TFF filtration methods and systems</li><li>
Understanding of key operating/scalable parameters for TFF/ultra filtration and ability to determine such parameters during process familiarization/optimization</li><li>
Provides technical support to lab or plant processes</li><li>
Works effectively in a team-oriented environment</li><li>
Presents work orally and in form of written development reports</li><li>
Adheres to GDP and SOPs in all aspects of work</li><li>
Independently plans and executes experiments, while working in a project team, toward development of viable commercial processes</li><li>
Demonstrates a clear understanding of technical issues and the requirements of a viable manufacturing process</li><li>
Executes procedures, processes, and methods for solutions to chemical and technical problems on a lab or plant scale</li><li>
Ensures that the chemistry is capable of meeting cost, yield, throughput, and QSHE goals on assigned processes</li><li>
Leads a team to accomplish the development, transfer, or implementation of technology at a lab or plant scale</li><li>
Develops and supports scalable processes and provides technical expertise and support during lab or plant operations</li></ul><h2 class="jobSectionHeader"><b>
</b></h2><h2 class="jobSectionHeader"><b>
LEADERSHIP &amp; BUDGET RESPONSIBILITIES</b></h2><div>
Demonstrates a positive attitude. Supports a positive, healthy, and flexible work environment that encourages employees and coworkers to develop their full potential and expand their horizons. This position has no supervisory responsibilities. Provides technical expertise to manufacturing.</div><h2 class="jobSectionHeader"><b><br>
</b></h2><h2 class="jobSectionHeader"><b>
SAFETY &amp; ENVIRONMENTAL RESPONSIBILITIES</b></h2><div>
Every individual is personally responsible for the safety and environmental aspects of their activities in the workplace. Each employee is expected to perform their job duties in a safe manner utilizing all their knowledge, training, ability, and experience.</div><div><b><br>
QUALITY RESPONSIBILITIES</b></div><div>
Corden Pharma Colorado (CPC) is a manufacturer of a variety of pharmaceutical products. In following Current Good Manufacturing Practices (cGMP), Corden Pharma Colorado manufactures in accordance with the US Food and Drug Administration (FDA), International Council for Harmonisation Q7 (ICH), and other global regulations as applicable. This is critical as it is our mission to not place patients at risk due to inadequate safety, quality, or efficacy. CPC&rsquo;s Quality Management System, which incorporates cGMP, is designed to deliver this quality objective. Attainment is produced through the requisite participation and commitment of all staff across departments and at all levels within the company.</div><div></div><div><br>
cGMP is the part of Quality Management System ensuring products are consistently produced to accurate quality standards. Adherence to clearly defined procedures, in compliance with the principles of cGMP, is required when performing operations across Corden Pharma Colorado.</div><div></div><h2 class="jobSectionHeader"><b><br>
QUALIFICATIONS</b></h2><div>
To perform this job successfully, an individual must be able to perform each essential duty satisfactorily. The requirements listed below are representative of the knowledge, skill, and/or ability required. Reasonable accommodations may be made to enable individuals with disabilities to perform the essential functions.</div><h2 class="jobSectionHeader"><b><br>
</b></h2><h2 class="jobSectionHeader"><b>
EDUCATION and/or EXPERIENCE</b></h2><div>
Bachelor&rsquo;s Degree (BS) in Organic Chemistry and 5 years related experience and/or training; or equivalent combination of education and experience. TFF/Untra filtration experience is required; and Peptide and GMP experience is a plus.</div><h2 class="jobSectionHeader"><b><br>
</b></h2><h2 class="jobSectionHeader"><b>
LANGUAGE SKILLS</b></h2><div>
Ability to read, analyze, and interpret common scientific and technical journals, financial reports, and legal documents. Ability to respond to common inquiries or complaints from customers, regulatory agencies, or members of the business community. Ability to develop bench scale laboratory procedures into step-by-step operating instructions for chemical operators. Ability to effectively present information to top management, public groups, and/or boards of directors.</div><h2 class="jobSectionHeader"><b><br>
</b></h2><h2 class="jobSectionHeader"><b>
MATHEMATICAL SKILLS</b></h2><div>
Ability to apply advanced mathematical concepts such as exponents, logarithms, quadratic equations, and permutations. Ability to apply mathematical operations to such tasks as frequency distribution, determination of test reliability and validity, analysis of variance, correlation techniques, sampling theory, and factor analysis.</div><h2 class="jobSectionHeader"><b><br>
</b></h2><h2 class="jobSectionHeader"><b>
REASONING ABILITY</b></h2><div>
Ability to apply principles of logical or scientific thinking to a wide range of intellectual and practical problems. Ability to deal with nonverbal symbolism (formulas, scientific equations, graphs, etc.) in its most difficult phases. Ability to deal with a variety of abstract and concrete variables. Ability to apply scientific methods to experimentally prove cause and effect.</div><h2 class="jobSectionHeader"><b><br>
</b></h2><h2 class="jobSectionHeader"><b>
CERTIFICATES, LICENSES, REGISTRATIONS</b></h2><div>
Domestic and international travel required.</div><h2 class="jobSectionHeader"><b><br>
</b></h2><h2 class="jobSectionHeader"><b>
PHYSICAL DEMANDS</b></h2><div>
The physical demands described here are representative of those that must be met by an employee to successfully perform the essential functions of this job. Reasonable accommodations may be made to enable individuals with disabilities to perform the essential functions.</div><div></div><div><br>
While performing the duties of this job, the employee is regularly required to talk or hear. The employee frequently is required to stand, walk, and sit. The employee must occasionally lift and/or move up to 25 pounds. Specific vision abilities required by this job include close vision, distance vision, and color vision.</div><h2 class="jobSectionHeader"><b><br>
</b></h2><h2 class="jobSectionHeader"><b>
WORK ENVIRONMENT</b></h2><div>
The work environment characteristics described here are representative of those an employee encounters while performing the essential functions of this job. Reasonable accommodations may be made to enable individuals with disabilities to perform the essential functions.</div><div></div><div><br>
While performing the duties of this job, the employee is occasionally exposed to fumes or airborne particles and low levels of toxic or caustic chemicals. The noise level in the work environment is usually moderate.</div><h2 class="jobSectionHeader"><b><br>
</b></h2><h2 class="jobSectionHeader"><b>
CORE COMPETENCIES</b></h2><div>
These are the specific areas of knowledge, skill and ability that are important for successful job performance. They must be job related and consistent with business necessity.</div><br>
<div></div><ul><li>
Demonstrates a positive attitude</li><li>
Strong background in chemistry or a related scientific field</li><li>
Working knowledge of regulatory issues in Pharmaceutical Manufacturing including cGMPs, GDP, FDA, PSM, OSHA, and EPA requirements</li><li>
Communicates effectively in writing and verbally within the department</li><li>
Computer skills, in the areas of: Microsoft Office Products (Word, Excel, PowerPoint), Chemdraw, and SciFinder</li><li>
Ability to work interactively within a multi-functional team-oriented environment</li><li>
Takes initiative in setting own goals and work plans</li><li>
Hands-on organic chemistry laboratory experience</li><li>
Has a broad technical knowledge in Organic Chemistry and Process Improvement Methodology</li><li>
Maintains a well-documented record of work performed in a laboratory notebook, laboratory reports, and campaign reports</li><li>
Experience in the synthesis and purification of peptides (desired)</li><li>
Has working knowledge of all plant-scale unit operations, scale-up, and plant design considerations</li><li>
Understanding of chemical reactivity, potential exotherms, cross reactivity, side products, and waste streams, especially for processes they support</li><li>
Regularly seeks out new learning opportunities beyond basic skills that can result in innovative approaches to technical issues</li><li>
Demonstrates clear understanding of technical issues and the requirements of a viable manufacturing process; has demonstrated independent support on multiple (not necessarily simultaneous) processes</li><li>
Identifies areas where change/continuous improvement is beneficial to the business, and successfully defends and implements projects</li><li>
Assumes reasonable risk in trying out new, self-generated ideas</li><li>
Proactive approach to problem identification and resolution</li><li>
Communicates effectively in writing and verbally within and across departments and to site management; updates are clear, selective, and effective</li><li>
Ability to understand and apply statistical design of experiments and draw sound conclusions from the results; uses results when solving problems or when proposing improvements</li><li>
Ability to provide leadership in all process chemistry aspects of manufacturing processes; leads teams in the development, transfer, troubleshooting, and improvement of chemical processes in interactive, interdisciplinary team environment</li><li>
Seeks out opportunities to learn manufacturing needs and methods that facilitate substantial process improvements; acquires new skills in state-of-the art technology and applies it to their assignments</li><li>
Demonstrates skills in negotiation and influencing others</li></ul><p><b>
SALARY</b></p><div>
Actual pay will be based on your skills and experience</div><div></div><h2 class="jobSectionHeader"><b><br>
BENEFITS</b></h2><ul><li>
401(k) matching - Corden Pharma will contribute 100% of the first 6% - 100% vested after 2 years of service</li><li>
Accident Plan</li><li>
Critical Illness Insurance</li><li>
Dental Insurance</li><li>
Disability Insurance</li><li>
Employee Assistance Program</li><li>
Flexible Spending Account</li><li>
Health Insurance PPO/HSA</li><li>
Hospital Indemnity Plan</li><li>
ID Theft Protection</li><li>
Life Insurance</li><li>
Paid Parental Leave</li><li>
Tuition Reimbursement</li><li>
Wellness Program</li><li>
Vacation &ndash; Three Weeks 1st Year</li><li>
Vision Insurance</li></ul><h2 class="jobSectionHeader"><b>
EQUAL OPPORTUNITY EMPLOYER</b></h2><div><i>
Corden Pharma provides equal employment opportunities to all employees and applicants for employment and prohibits discrimination and harassment of any type without regard to race, color, religion, age, sex, national origin, disability status, genetics, protected veteran status, sexual orientation, gender identity or expression, or any other characteristic protected by federal, state, or local laws. Corden Pharma embraces fair hiring practices.</i></div><p></p><p><br>
This post will expire December 12, 2025</p></div>

Sr. Process Chemist - TFF focus

WALKER COLE INTERNATIONAL LTD

<p>We're partnering with a global biopharmaceutical organisation looking for a Production Technician (Purification) to join their team in Surrey. This role plays a key part in the large-scale purification of antigens used in vaccine production.</p><p>You'll work within a graded laboratory in the restricted area of the production plant, maintaining the highest standards of GMP, HSE, and biosecurity, while supporting cross-functional collaboration across teams. This position requires flexibility, including weekend shift cover.</p><p><strong>Key Responsibilities</strong></p><ul><li>Manufacture purified antigens efficiently and cost-effectively, meeting all GMP, HSE, and biosecurity requirements</li><li>Operate and maintain process equipment in line with SOPs</li><li>Perform in-process testing and record data accurately</li><li>Document and report deviations or investigations in collaboration with QA</li><li>Carry out aseptic manipulations of products</li><li>Monitor plant and laboratory equipment data, taking corrective actions as required</li><li>Work closely with other shift technicians to ensure seamless handovers</li><li>Support weekend and holiday shift cover as needed</li><li>Maintain a clean, compliant workspace and contribute to continuous improvement initiatives</li></ul><p><strong>About You</strong></p><ul><li>Experience in pharmaceutical or biopharmaceutical manufacturing</li><li>Understanding of GMP and working within a quality system</li><li>Confident using IT systems and electronic documentation tools</li><li>Proactive, adaptable, and able to work independently</li><li>Strong communication and teamwork skills</li><li>Detail-oriented, methodical, and safety-focused</li></ul><p>If you're looking for a hands-on production role in a highly regulated environment with excellent team culture and development opportunities, this could be a great fit.</p><img src="https://www.jobg8.com/Tracking.aspx?n70Gs5vBCd%2bwkzmad4jXBntF2qFlWcV2f" width="0" height="0" />

Production Technician - Purification

SCHOTT Technical Glass Solutions GmbH

Wir ermöglichen was unmöglich scheint. Denn bei SCHOTT wissen wir, dass gemeinsame Verantwortung, Erfahrung und enge Kollaboration bahnbrechende Lösungen hervorbringen. Als globaler Konzern für Materialtechnologie finden wir so neue Wege, eine bessere Zukunft zu gestalten - für unsere Partnerunternehmen, unsere KundInnen und unsere MitarbeiterInnen.<br> <br><b>Aufgaben . klicken sie bewerben, für die volle Stellenbeschreibung<img src="https://www.jobg8.com/Tracking.aspx?b60HxLecPg5DxfRrE4cABeORCMpJanQYo" width="0" height="0" />

Technikerin Prozesstechnik (m/w/d)

Glow Beauty On Demand

<br><b>Job Title</b><br>Prototype Equipment Technician - Chemical Process Industry - Dubai UAE<br>Job Description<br>Prototype Equipment Technician - Chemical Process Industry - Dubai UAE<br> <br>Role Summary<br> <br>Cabot is hiring a Prototype Equipment Technician to support its R&amp;D and engineering teams in Dubai. This role focuses on the design, fabrication, calibration, and maintenance of chemical process equipment and electro-mechanical systems. The ideal candidate will have hands-on experience with assembling and testing prototype systems, along with a deep understanding of chemical plant operations and instrumentation.<br> <br>Job Details<br> <br>Job Location: Dubai, UAE<br>Industry: Chemicals<br>Function: Equipment Maintenance / Engineering Support<br>Gender: Any<br>Candidate Nationality: Any<br>Candidate Current Location: Any<br>Job Type: Full-time<br> <br>What You ll Do<br> <br>* Participate in designing and building chemical process prototypes, including plumbing and electrical subassemblies<br>* Collaborate with engineers to install, test, and optimize new process systems<br>* Perform equipment calibrations, preventive maintenance, and system upgrades<br>* Maintain detailed records and documentation for specifications, manuals, and procedures<br>* Assist in system automation and troubleshooting of electro-mechanical processes<br>* Support Responsible Care  initiatives to uphold environmental, health, and safety standards<br>* Deliver consistent technical support on project tasks and respond to system faults proactively<br> <br>Ideal Profile<br> <br>* Post-secondary technical training (diploma or certification in engineering/technician programs)<br>* 3 5 years hands-on experience in chemical plant equipment maintenance or prototype testing<br>* Familiarity with industrial automation systems, electrical components, and safety standards<br>* Strong mechanical aptitude and ability to interpret technical drawings<br>* Detail-oriented, self-motivated, and capable of managing multiple tasks efficiently<br>* Excellent problem-solving skills and communication abilities in a team environment<br><br>

Prototype Equipment Technician

(QAFAC) Qatar Fuel Additives Company Limited

<div>
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  <strong>
   The Materials Technician - Stock is responsible for managing the issuance, receipts, and returns of materials physically, performing accurate SAP data transaction entry and maintaining detailed stock records. The role involves receiving and handling bulk chemical deliveries, and ensures that accurate records of the quantities and location of all items are maintained.
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   Job-Specific Responsibilities
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   Administration
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   Carry out formalities required in issuance, receipts, and returns, including real-time data entry in SAP, work orders / material reservation processing and closing, material inspection intimation and follow-ups, Overage, Shortage &amp; Damage (OS&amp;D) preparation, material labeling, and tag generation.
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   Process Material Receipt Voucher (MRV) for invoices involving payment and send them to Finance for final payment processing.
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   Bulk Chemical Deliveries
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   Receive bulk chemical tankers, prepare gate passes, weigh bulk tanker deliveries, and obtain necessary approvals from safety and operations departments.
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   Inventory Management
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   Support stock checks and inventory reviews to determine material holdings, performing stock counts and assisting in reconciling inventory variances (incl. year-end and perpetual inventory counts to resolve discrepancies and finalize items for write-off).
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   Conduct complete cycle activities for consumables, PPE, spare parts, and chemicals to measure inventory accuracy and reconcile discrepancies before year-end stock taking.
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   Submit noted discrepancy lists and final discrepancy reports to Materials Controller.
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   Maintain detailed stock records and operate control systems to ensure required materials levels.
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   Issue Control
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   Issue materials according to approved procedures, as per work orders &amp; reservations ensuring requisitions and authorized deliveries are correctly processed.
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   Permits Administration
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   Obtain and process permit approvals from safety, i.e., cold work, vehicle entry permits, crane lifting / load charts and other permits required for executing required task.
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   Ensures proper permit closing after job completion and filing.
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   Documentation
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   Maintain files and records for gate passes, material issuance, receipt &amp; return vouchers, permits, and material receipt vouchers (MRV) along with other copies of supporting documents, i.e., invoices, purchase orders, delivery notes, certificate of conformity / completion, MSDS, Airwaybills, etc.
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   Reporting
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   Submit monthly data on warehouse activities and KPIs for the completion of monthly operational reports
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   Materials Labelling
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   Ensures all materials entering or leaving the warehouse are correctly labelled for identification with their assigned storage locations in the warehouse for traceability.
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   General Responsibilities
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   Compliance
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   Adhere to QAFAC&rsquo;s safety, quality, and environmental standards to guarantee employee safety, product quality, and environmental compliance.
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   KEY RESULT AREAS
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   Accurate and timely SAP data entry for all material transactions.
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   Effective monitoring and maintenance of chemical tank levels to ensure uninterrupted operations.
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   Successful completion of year-end and perpetual inventory counts with minimal discrepancies.
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   Efficient and accurate issuance of materials to authorized personnel according to requisitions.
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   Accurate materials identification and materials traceability.
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  JOB REQUIREMENTS
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   Minimum Qualifications:
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   Diploma in an Engineering Discipline / Supply Chain Management.
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   Minimum Experience:
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   Minimum of 2 years of experience in a similar position at an oil &amp; gas or petrochemical company.
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Materials Technician-Stock

Octapharma Pharmazeutika Produktionsges.m.b.H.

<p>Octapharma is one of the largest human protein manufacturers in the world, developing and producing human proteins from human plasma and human cell lines. We employ more than 11,000 people worldwide to support the treatment of patients in 120 countries with products across three therapeutic areas: Immunotherapy, Haematology and Critical Care. With seven R&D sites and five state-of-the-art manufacturing facilities in Austria, France, Germany, and Sweden, Octapharma also operates over 195 plasma donation centres across Europe and the US. With four decades of experience, we are committed to advancing patient care worldwide.</p> <p>Octapharma ist auf die Entwicklung und Herstellung von hochreinen Arzneimitteln aus menschlichem Blutplasma spezialisiert. Als Teil eines Familienunternehmens ist Octapharma Wien nicht nur der größte Produktions-, sondern auch ein erfolgreicher Forschungsstandort der Octapharma Gruppe. Da unser Standort laufend wächst, suchen wir ab sofort zur Verstärkung unseres Teams einen <b>Verfahrenstechniker (m/w/d) - Purification 1 - Befristung</b>.</p><br /><b>Aufgaben</b> <ul> <li>Überprüfung und Einstellung der pH-Werte und der gewünschten Konzentration</li> <li>Durchführung der Ultrafiltration und Diafiltration</li> <li>Einstellen der vorgeschriebenen TemperaturintervalleI</li> <li>Durchführen der Chromatographieschritte</li> <li>Überprüfung und Einhaltung der Zeitvorgaben</li> <li>Demontage, Reinigung und Wartung der Geräte</li> <li>Einhalten der GMP-Vorgaben</li> </ul><br /><b>Profil</b> <ul> <li>Abgeschlossene chemische oder technische Berufsausbildung (z.B. Verfahrenstechnik, Fachschule Rosensteingasse, etc.)</li> <li>Idealerweise Berufserfahrung in der Pharma- oder Lebensmittelindustrie</li> <li>Sehr gute Deutschkenntnisse in Wort und Schrift</li> <li>EDV-Grundkenntnisse</li> <li><b>Bereitschaft zur Arbeit im vollkontinuierlichen Schichtbetrieb (Mo-So, von 06:00-18:00 und 18:00-06:00 Uhr) ist Voraussetzung</b></li> <li>Verantwortungsbewusstsein, Flexibilität und Teamfähigkeit</li> <li>Genaues Arbeiten entsprechend den Herstellvorschriften bzw. GMP-Richtlinien</li> </ul><br /><b>Wir bieten</b> <p>Diese Position wird <b>befristet bis 31.07.2026 im Ausmaß von 38 Wochenstunden</b> gesucht.</p> <ul> <li>Vielseitige Aufgaben in internationalem Umfeld, Flexibilität und Eigenverantwortung</li> <li>Verlässlicher Arbeitgeber mit großzügigen Sozialleistungen und marktüblicher Bezahlung.</li> <li>Vertraute Umgebung eines Familienunternehmens mit Benefits wie Do & Co Betriebsrestaurant, außergewöhnlichen Mitarbeiter:innen-Events und vielen mehr:<br></li> </ul> <p><b>Zusätzliche Informationen:</b><br></p> <p>Das KV-Mindestbruttogehalt (Chemische Industrie) für Ihre neue Position beträgt EUR 3.395,16. Wir sind bestrebt Ihr Gehalt an Ihr Profil und Ihre Qualifikationen anzupassen, daher besteht die Bereitschaft zur Überzahlung.</p> <p>Wir freuen uns über neue engagierte Mitarbeiter innen, mit denen wir unser starkes Wachstum gemeinsam vorantreiben können, um unseren Patienten weiterhin ein besseres Leben zu ermöglichen-denn es liegt uns im Blut!</p><br/><p>JBG81_AT</p><img src="https://www.jobg8.com/Tracking.aspx?vwKBUUP%2bHlGYumd2h3uwodDzNv92Pbdnn" width="0" height="0" />

Verfahrenstechniker (m/w/d) - Purification 1 - Befristung

Ernest Gordon Recruitment Limited

<p><strong>Lead Site Fitter (Process Industry Sites)</strong><strong>£45,000 - £50,000 DOE + Bonus + Van + Private Medical + Enhanced Pension + Full Industry Training</strong><strong>Horsham</strong>Are you a skilled mechanical engineer who has an eye for detail and is looking for your next career opportunity with a company that provides ample training and development to set you up for a great career, whilst rewarding you with an excellent remuneration package and fantastic perks?On offer is a varied role where you will cover a regional patch, which would suit a candidate with experience in electrical/mechanical engineering. This role requires you to carry out routine and reactive maintenance on processing plants at client sites.In this senior role, you will be responsible for the health and safety, RAMS, and mentoring and training on site, as well as carrying out maintenance and repairs of the process equipment.This company, established 40 years ago, is currently going through its strongest growth period to date due to its level of experience, reputation, technical knowledge, and well-established contracts.This role will see you travel to clients' sites, servicing and fault-finding processing equipment. If you have experience in mechanical fitting and hold a valid CSCS card, then this may be the job for you.<strong>The Role:</strong></p> <ul> <li>Lead and manage a small team</li><li>Hot Air Welding and solvent welding of plastics</li><li>Able to work at heights (occasionally over 12m), with equipment and to lift and manipulate heavy objects following appropriate safety practices</li><li>Drilling, Steel cutting, Chemical handling, Cleaning and Operation of mechanical lifting equipment</li><li>Mechanical assembly and operation of machinery, power tools, and hand tools</li></ul> <p><strong>The Person:</strong></p> <ul> <li>Experience as a fitter/technician in the process industry</li><li>Engineering qualification with PASMA, CSCS card, and RAMS experience</li><li>Full UK Drivers Licence</li></ul> <p>If you're interested in this role, click 'apply now' to forward an up-to-date copy of your CV.Reference Number: BBBH21515The salary advertised is a guideline for this position. The offered remuneration will be dependent on the extent of your experience, qualifications, and skill set.</p><img src="https://www.jobg8.com/Tracking.aspx?Z3TFjo9onGn063qTgGwjgkvfL8pD52%2fHk" width="0" height="0" />

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