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Electro-Mechancial Technician

Sunbury-Upon-Thames

Proactive Global is hiring for experienced Electromechanical Technicians having hands-on work experience with Mechanical and Electrical Components for a leading manufacturing organisation in Sunbury-on-Thames.

This is a Permanent Position

Shift Timings : Mon-Friday 8:00AM - 4:30PM

Salary - £30k per annum

Responsibilities:

Carry out electro-mechanical assembly work on all products, working to drawings, parts lists, procedures, and workinstruction.Carry the testing on all products, working to drawings, parts lists, procedures, and workinstruction.Work on prototype work when required.Authorised to carry out inspection processes in line with QA procedures on all products when required.Conform when applicable to company quality management systems procedures.Carry out any packaging requirements.

Interested candidates can share their CV at [email protected] or contact Gaurvi at +44 (0) 1784 919765 for further discussion on the role. Alternatively, apply directly to this Advert!

Proactive Global is committed to equality in the workplace and is an equal opportunity employer.
Proactive Global is acting as an Employment Business in relation to this vacancy.

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Electromechanical Production Technician - Sunbury, TW16

Proactive Global is currently recruiting a highly organised Production Technician with experience in mechanical/electronic assembly, ideally with exposure to the medical device industry.

This is a great opportunity for an experienced Electromechanical Production Technician to join a small but growing team of assemblers and technicians. The successful applicant will be self-motivated with a good understanding of mechanical and electrical assembly and quality control.

Key Responsibilities

Carry out electro-mechanical assembly work on all products, following drawings, parts lists, procedures, and work instructions.Conduct testing on all products, working to drawings, parts lists, procedures, and work instructions.Work on prototype projects when required.Carry out inspection processes in line with QA procedures on all products when needed.Follow company quality management system procedures where applicable.Complete any packing requirements.Follow all H&S guidelines as set out in drawings, parts lists, procedures, work instructions, risk assessments, and QA procedures.

Skills and Experience

Self-motivated.Ability to work effectively within a small team.Experience with mechanical/electronic assembly, ideally in medical devices.Understanding of quality control and QA processes.

If you have the above skills and wish to be considered for this position or find out more details then please contact Joanna Siedlecka on 07500607229 or submit your CV to [email protected] or alternatively, apply to this advert!

Proactive also offer a referral scheme for successful applicants - if you know anyone that could be suited to this position then please contact Proactive with there details and if they are placed by Proactive you will receive £250. *T&Cs apply*

Proactive Global is committed to equality in the workplace and is an equal opportunity employer.
Proactive Global is acting as an Employment Business in relation to this vacancy.

Proactive Global is committed to equality in the workplace and is an equal opportunity employer.
Proactive Global is acting as an Employment Business in relation to this vacancy.

Proactive Global is committed to equality in the workplace and is an equal opportunity employer.
Proactive Global is acting as an Employment Business in relation to this vacancy.

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Quality Assurance (QARA)Administrator

Sunbury-Upon-Thames

Proactive Global is looking for Quality Assurance Administrator (QARA) for a leading pharmaceutical products manufacturer based in Sunbury, TW16 Location.

This is a permanent position.

Salary - £28-30K Per annum

Key Responsibilities:

Quality Assurance:

Maintain and update the Quality Management System (QMS) in accordance with ISO 13485 and internal procedures.Administer document control processes, ensuring timely revision, approval, and distribution of controlled documents.Support CAPA, non-conformity (NC), complaint handling, and change control processes.Assist with internal and external audits (Notified Bodies, FDA, suppliers).Ensure training records are accurate, complete, and up to date.Monitor calibration, equipment maintenance, and environmental controls as required.

Regulatory Affairs:

Assist in preparing documentation for the filing of regulatory submission.Manage registration activities for products in various markets (MHRA, EUDAMED, etc.).Support with keeping up to date with regulatory landscape changes by identifying and documenting gaps.

Qualifications and Experience:

Bachelor's degree in a relevant field (e.g., Quality Management, Engineering, or related discipline).Experience in a regulated environment (preferably medical devices or pharmaceuticals).Understanding of ISO 13485, EU MDR, and/or FDA QSR requirements.Strong organisational and administrative skills.Excellent attention to detail and accuracy.Proficiency in MS Office (Word, Excel, Outlook, Teams).

Interested candidates can directly apply to this Advert or share their CVs at [email protected] or call at +44 1784771135 for further discussions.

Proactive Global is committed to equality in the workplace and is an equal opportunity employer.
Proactive Global is acting as an Employment Business in relation to this vacancy.

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Site Director

Sunbury-Upon-Thames (Permanent Position)

Proactive Global is hiring for a well experienced Site Director for a leading Manufacturing organization based in Sunbury-Upon-Thames. The Operations Manager & Site Lead is responsible for leading all day‑to‑day site operations, ensuring that production, quality, logistics, and facilities run efficiently, safely, and in alignment with strategic objectives.

This role also plays a key part in integrating new product lines, establishing the supporting operational processes, and optimising the physical site layout to enable efficient flow, scalability, and future growth.

Salary - £80-£100k per annum

Key Responsibilities

Oversee all daily operations across production, warehousing, logistics, and site services to ensure smooth and efficient output.Translate production and sales planning into operational schedules.Lead the operational integration of new product linesinto the site, ensuring smooth transition from engineering/R&D into production.Develop, implement, and embed new processes, SOPs, and work instructions required to support product introductions.Collaborate with Engineering, R&D, QA/RA, and Supply Chain to ensure manufacturing readiness, capability, and regulatory compliance.Drive validation of new processes (e.g., pilot runs, capability checks, ramp‑up plans).Evaluate, redesign, and optimise the site's physical layoutto improve efficiency, material flow, and capacity.Implement lean principles to minimise waste, streamline workflows, and support future operational scale.Partner with Facilities, Production, and Engineering to ensure layout changes support safety, quality, and regulatory requirements.Act as the senior on‑site leader, responsible for workforce planning, team development, and employee engagement.Lead, mentor, and support team leads and supervisors to maintain high performance and accountability.Manage employee relations in partnership with HR and foster a positive, inclusive working culture.Ensure adherence to internal SOPs, QMS (e.g., ISO 13485), and medical device regulatory standards.Partner with QA/RA to manage non‑conformances, CAPA activity, and audit readiness.Promote a culture of right‑first‑time quality and continuous improvement.Ensure material availability, inventory accuracy, and effective stock controls to support production demands.Work with purchasing, engineering, and suppliers to resolve material, build, or supply issues promptly.Ensure Health & Safety compliance for the site, Oversee site maintenance, calibration and contractor management.Lead site risk assessments, emergency procedures, and business continuity planning.Support engineering changes, new product introductions, and commercial needs across the organisation.

Skills & Experience Required

Experience in the life sciences industry or working with life‑science‑related products is strongly preferred.Experience with ISO 13485 or other highly regulated QMS environments.Proven experience managing operations within a manufacturing or technical environment.Strong leadership skills with experience managing multi‑disciplinary teams.Experience implementing new processes, ideally for new product introductions (NPI).Ability to understand technical documentation (drawings, parts lists, build instructions).Knowledge of lean principles and continuous improvement methodologies.Strong organisational, communication, and problem‑solving skills.Experience in regulated environments, preferably medical devices or similar

Interested candidates can directly apply to this Advert or share their CV at [email protected] . For further details, connect with Guarvi at +44 1784771135.

Proactive Global is committed to equality in the workplace and is an equal opportunity employer.
Proactive Global is acting as an Employment Business in relation to this vacancy.

Read less