Team Lead - Cleanroom Job at Connexion Systems & Engineering, Inc (Manchester)

Senior Construction Project Manager

AMTS is looking for a proven Senior Construction Project Manager with a strong u...

Location

Salary:

Not provided

AM Technical Solutions

Expiration Date

Until further notice

Requirements

Minimum 10-15 years experience in similar pharmaceutical cleanroom environments
Must have led cleanroom installation teams
Must be experienced in cleanroom system components from multiple manufacturers to include pharma systems
Must understand project programming from start to finish to ensure successful project execution
Must have a bachelors degree in Engineering or Construction or related experience
Able to communicate verbally, electronically and written to convey information in an effective manner
Technically skilled to act as the interface between disciplines, engineers, installers and contractors
Needs to understand equipment and system P&IDs, specifications and drawings and be able to identify field discrepancies for resolution
Understanding of Area Layout
Knowledge of micro schedule for pre-facilitation, understanding of sequence of construction activities and install sequencing

Job Responsibility

Project Planning and Design: Collaborates with clients, designers, and engineers to define project scope, objectives, and requirements, ensuring compliance with relevant regulations and industry standards
Budget Management: Develops and manages project budgets, ensuring projects are completed within allocated resources
Schedule Management: Develops and monitors project schedules, ensuring timely completion of all project phases
Construction Management: Oversees the construction process, ensuring quality control, safety, and compliance with all relevant regulations
Client Communication: Serves as the primary point of contact for the client, keeping them informed of project progress and addressing their concerns
Validation and Testing: Manages the validation and testing process to ensure the cleanroom meets all design specifications and performance requirements
Risk Management: Identifies and manages potential risks and issues that may affect the project’s success
Team Leadership: Leads and motivates project teams, providing guidance and support to ensure the project’s success
Documentation: Maintains accurate and comprehensive project documentation, including as-built drawings, validation reports, and other relevant documents

Supervisor, Manufacturing

Lead the manufacturing function within budget and output targets to meet custome...

Location

Malaysia , Batu Kawan, Penang

Salary:

Not provided

Sandisk

Expiration Date

Until further notice

Requirements

Minimum bachelor degree in management / engineering
Good knowledge in 6S / Safety & ESD production environment
Able to give full support during off/rest day as well (if required)
Able to work 12hours & Class 1K cleanroom

Job Responsibility

Lead the manufacturing function within budget and output targets to meet customer requirements and standards
Full accountability for ensuring safety, customer quality, cost and delivery requirements are met
Responsible for developing an enthusiastic, motivated and flexible team by building working relationships ensuring that Health, Safety and Environmental requirements are adhered to
Manage the team on best practice and establish standard policies and procedures whilst also mentoring and leading teams
Implement and manage continuous improvement and modern manufacturing principals by highlighting deficiencies and recommending changes in training, working practices and processes
Effectively and efficiently manage the production to meet the daily/weekly/monthly targets, meeting quality and delivery expectations, minimizing costs where possible and ensure the required best working practices are maintained at all times
Manage, coach and develop a high performing manufacturing team that meets agreed objectives, and which delivers best practice results, added value and continuous improvements
Ensure that the function operates in accordance with any health, safety and environmental policies and procedures to ensure the safety and wellbeing of workers and visitors
Maintains a high standard of 6S environment

Fulltime

Electrical engineer

We are looking for an Electrical Engineer – Lead/Manager for Power Distribution ...

Location

United States

Salary:

Not provided

AM Technical Solutions

Expiration Date

Until further notice

Requirements

10 – 15 years of progressive Electrical Engineering and leadership experience
Experience leading a technical team
Experience developing staff capabilities, techniques and tools
Experience using Electrical Analysis and Design Software to complete assigned work: Examples: SKM, Revit, AutoCAD MEP, Visual Lighting Studio or equivalent lighting design software
Knowledge of sub-station and building switchgear design and operations
Knowledge of Instrumentation and Controls engineering
Written and oral communication (English language) skills including specification writing, field reports, general and keynotes, submittal reviews, and email
Comfortable working independently in a fast-paced, dynamic and collaborative environment
Knowledge of Short Circuit Analysis, Fault Current Analysis
Knowledgeable in National Fire Protection Association/National Electrical Code (NFPA/NEC) Standards, and IEEE/IES/API Standards

Job Responsibility

Develop designs for building and equipment power distribution systems, lighting, and controls, focusing on cleanrooms and advanced laboratories
Design and Engineering work may include the following: Campus or Site power sizing and distribution
Cleanroom and Laboratory Electrical Power sizing and distribution
Lighting and Controls
Experience with instrumentation and controls for mechanical, electrical, and process is a plus
Electromagnetic Interference (EMI) analysis, modeling, and abatement
Tel/Data systems
Using software such as SKM, Revit, Visual Lighting Studio, and others
Feasibility Studies
Basis of Design and Schematics

Senior Manager, Mechanical Engineering

Veeco has an opening in Plainview, NY, for a Senior Manager, ETO (Engineer-To-Or...

Location

United States , Plainview

Salary:

159000.00 - 200000.00 USD / Year

Veeco Instruments

Expiration Date

Until further notice

Requirements

Bachelor’s or Master’s degree in mechanical engineering is required
A minimum of 10 years of experience with engineering design and development and experience in semiconductor equipment or other capital equipment is preferred
A minimum of 5 years in an engineering leadership position performing new product development is required
Ability to lead a multi-disciplinary engineering team in the design of complex technical equipment with a team comprised of direct employees, consultants, and temps
Ability to manage multiple ongoing projects, priorities, and risks within specified time and budgetary restrictions
Ability to estimate, plan, schedule, and allocate resources for engineering activities
Strong working knowledge and application of mechanical engineering principles
Possess a system-level understanding of electro-mechanical systems, including a working knowledge of electrical and software principles
Ability to interpret engineering drawings, system block diagrams, electrical schematics, engineering specifications, and manufacturing requirements is required
In-depth understanding of the product life cycle (PLC) and phase gate review process

Job Responsibility

Manage and lead mechanical, electrical, and program management resources, as well as matrix-managed software resources, with full ownership and responsibility to execute new tool and upgrade ETO projects through all phases of the product lifecycle, including concept, prototyping, development, qualification, production support, and field support
Coordinate the completion of milestones for critical product development programs while making effective use of internal and outsourced resources
Participate in customer requirements and specification reviews with a cross-functional group, including Marketing and Operations, prior to quote delivery
Upon purchase order acceptance, work closely with Marketing and Operations to translate customer process requirements into system configurations and design requirements
Plan, schedule, and resource engineering activities in coordination with the Operations build schedule and committed delivery dates
Provide Engineering support to Operations during the manufacturing build process
Drive all engineering documentation and deliverables, including product BOM’s, P&IDs, and engineering drawings, to be prepared, updated, and released in accordance with applicable company format and procedural requirements
Provide technical support for escalations on released and ETO products when additional support is requested by Field Service or Operations personnel
Ensure compliance with applicable industry safety and regulatory standards
Manage internally and externally sourced engineering changes (ECs) that are compliant with the Veeco change process and in support of program schedule requirements

What we offer

Medical, Dental, and Vision
Employee Stock Purchase Plan (ESPP)
401(k) with Company Match
Holiday, Vacation, and Sick Time
Flexible Spending Accounts (FSA)
Commuter Benefits
Life and Accident Insurance
Disability Insurance
Tuition Reimbursement
Employee Assistance Program (EAP)

Fulltime

Sterile Pharmacy Operations Manager

The Sterile Pharmacy Operations Manager is responsible for the leadership, coord...

Location

United States , Tampa

Salary:

150000.00 - 180000.00 USD / Year

Strive Compounding Pharmacy

Expiration Date

Until further notice

Requirements

Bachelor of Science (BS) in Pharmacy, Doctor of Pharmacy (PharmD)
Active state pharmacist license in good standing
Board Certified Sterile Compounding Pharmacist (BCSCP)
2+ years of experience in sterile compounding or pharmacy production
1–2 years of leadership or supervisory experience required
Strong understanding of USP <797>, USP <795>, USP <800>, cGMP/503B guidelines, and sterile production workflows
Proficiency in pharmacy calculations, aseptic technique, and sterile compounding documentation standards
Excellent organizational, time management, and multitasking abilities
Strong interpersonal and communication skills, with proven ability to lead, mentor, and develop teams

Job Responsibility

Provide daily leadership, supervision, training and performance management for the sterile compounding team
Assign compounding and preparation tasks based on technician skillset, training progress, performance history, and workflow needs
Support staffing and scheduling decisions, including shift planning, hood rotation schedules, and daily workload distribution
Oversee daily sterile production workflows to ensure efficiency, compliance, and on-time completion of critical lots
Manage and support “outside-the-hood” duties including equipment preparation, autoclaving, oven operations, cleanroom resupply, labeling tasks, and end-of-day organization
Ensure all facility and equipment readiness requirements are met, including cleanliness, maintenance, calibration, and required documentation
Verify patient-specific prescriptions, compounded lots, and batch records, ensuring accuracy, completeness, and adherence to SOPs
Perform or oversee required pharmacy calculations and validate ingredient measurements for potency and accuracy
Ensure strict adherence to USP <797>, USP <795>, USP <800>, 503B guidance, 21 CFR 211 (cGMP), and all applicable state and federal regulations
Maintain policies related to aseptic technique, gowning, environmental controls, and cleanroom behavior

What we offer

Employer paid healthcare coverage available after 30 days of employment
Choice of an FSA/HSA
Voucher for new hire scrubs (if applicable)
Parental leave
401(k) plan with matching contributions
Weekends and holidays off
FREE COMPOUNDED MEDS to employees and immediate family members

Fulltime

New

Graduate Quality Engineer

The Quality Graduate will rotate between areas of the quality department. These ...

Location

Ireland , Fermoy

Salary:

Not provided

Sanmina

Expiration Date

Until further notice

Requirements

Minimum Level 7 Degree/ Diploma (Preferably in a Biotechnology, Microbiology, Science, Electronics, Mechanical or Industrial Engineering)
Proficient in the use of MS Word, Power-point and Excel
Ability to write standard operating procedures, training documents, and regulatory responses is preferred
Ability to respond to common inquiries or complaints from internal customers and regulatory agencies
Flexibility to Travel
Experience in Cleanrooms (ISO Class 8),is preferred
Sound understanding and utilization of Problem Solving Techniques
Good communication and influencing skills

Job Responsibility

Management of closed loop customer complaints and improvement processes
Generation and Review and review of Quality Metrics System
Overall responsibility for DMR/DHR and Technical Files
Data collection, analyzing and reporting
Pareto and trend analysis
Initiate and drive Continuous Improvement programs
NPI Approval including First Article Inspections and Reporting
CAPA, NCM and RMA analysis and Improvement
QSR Validation protocols and report (IQ, OQ & PQ)
Conducting Audits to ensure conformance and effectiveness of the Quality System

New

Assembler III, Imaging, 2nd

Shift: Monday- Friday 3:30pm to 12:00AM. Occasional overtime during the week and...

Location

United States , Charlton

Salary:

18.51 - 23.17 USD / Hour

KARL STORZ

Expiration Date

Until further notice

Requirements

High school diploma, or equivalent experience
2-4 years of experience assembling miniature precision medical products preferred
Substantial understanding of imaging assembly, or proficient with multiple moderately complete imaging assemblies
Ability to understand assembly drawings and written assembly procedures
Ability to operate moderately complicated machinery
Ability to meet takt time and quality standards
Ability to work with adhesives, solvents, microscopes, small hand and power tools, measurement devices and other related tools and equipment
Ability to work well with coworkers
Must be able to work overtime as needed
Must be punctual, able to sustain attendance guidelines, and work hours as assigned

Job Responsibility

Assemble quality endoscope imaging systems while adhering to prescribed standards
Perform moderately difficult assembles of various intricate optical and mechanical components
Perform cleaning and inspection of various components using hand tools and ultrasonic baths
Load/unload ovens
Follow prescribed assembly techniques and within assigned time standards to produce quality endoscope sub assemblies while meeting productivity guidelines
Perform five or more tasks efficiently of the following: all functions of an Assembler II as well as final assembly, Inspection, count inventory, fill in for manufacturing coordinator, DTA training, DHA training, lead safety huddles
shift trainer
Actively participate in company sponsored training program
Cross train in other value stream assemblies as needed
Understand the process flow on assigned tasks (suppliers/customers) and the impact of their decisions

What we offer

Medical / Dental / Vision including a state-of-the-art wellness program and pet insurance
3 weeks vacation, 11 holidays plus paid sick time
Up to 8 weeks of 100% paid company parental leave
401(k) retirement savings plan providing a match of 60% of the employee’s first 6% contribution
Section 125 Flexible Spending Accounts
Life, STD, LTD & LTC Insurance
Tuition pre-imbursement up to $5,250 per year
Fitness reimbursement of up to $200 annually

Fulltime

Sterility Assurance Lead

This is a critical leadership role responsible for ensuring that all marketed an...

Location

Ireland , Cork

Salary:

Not provided

BioMarin Pharmaceutical

Expiration Date

Until further notice

Requirements

Bachelor’s degree in Microbiology, Biology, Pharmaceutical Sciences, or related discipline (Master’s or PhD preferred)
10–15+ years of progressive experience in microbiology within GMP-regulated pharmaceutical or biotechnology environments
Minimum 5 years in leadership roles, with proven ability to influence cross-functional teams and senior stakeholders
Significant hands-on experience supporting aseptic sterile fill-finish operations, preferably with isolator qualification and maintenance
Strong knowledge of EU GMP Annex 1 and global sterility assurance standards
Demonstrated success in leading contamination investigations and regulatory interactions
Strategic thinker with strong problem-solving and decision-making abilities
Excellent communication and influencing skills across all organizational levels
Ability to interpret complex microbiological data and translate into actionable strategies

Job Responsibility

Strategic Leadership: Own and continuously evolve the site’s Contamination Control Strategy, ensuring alignment with global standards and regulatory requirements
Regulatory Compliance & Influence: Implement regulatory expectations, maintain compliance with EU GMP Annex 1, 21 CFR, USP, EP, JP, and ICH guidelines, and stay current with emerging global regulations, audit trends and best practices
Training & Culture: Design and deliver robust training programs on aseptic processing, behaviors, and contamination control principles to embed a culture of sterility assurance across the site
Environmental Monitoring & Utilities: Establish and maintain environmental monitoring and clean utilities programs, ensuring proactive contamination control
Technical Expertise: Provide expert input on gowning, cleaning, sanitization & sterilization strategies, microbiological method transfers, and contamination investigations
Investigations: Lead and guide the investigation of contamination-related deviations, non-conformances, and sterility failures. Perform root cause analysis, define corrective and preventive actions (CAPAs), and ensure timely closure of quality events
Data Analysis & Risk Mitigation: Review microbiological data trends, identify risks, and implement effective mitigation strategies
Global Collaboration: Partner with global Technology and Quality functions to ensure site alignment with industry best practices and BioMarin network standards
Continuous Improvement: Drive initiatives to enhance microbiological quality, operational efficiency, and inspection readiness
Facility Expansion Support: Lead microbiology aspects of facility expansions, including cleanroom qualification and sterilization systems

Team Lead - Cleanroom

Connexion Systems & Engineering, Inc

Location:
United States , Manchester

Category:
Manufacturing

Contract Type:
Not provided

Salary:

Job Description:

Job Responsibility:

Requirements:

Nice to have:

Additional Information:

Job Posted:
January 08, 2026

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