Manufacturing Technician- Pharmaceutical Job at SRG (Stirling)

Senior Manufacturing Process Technician

In this role you will be operating an automated and innovative manufacturing equ...

Location

United States , New Albany

Salary:

65840.00 - 82251.00 USD / Year

Amgen

Expiration Date

Until further notice

Requirements

High school diploma and 2 years of technical experience in Pharmaceutical, Manufacturing, or Packaging environment
Associate’s degree and 6 months of technical experience in Pharmaceutical, Manufacturing, or Packaging environment
Ability to follow written procedures
Ability to stand or sit for extended periods of time
Ability to lift 35 pounds
Capability to diagnose malfunctions and perform equipment setup
Educational Background in Mechanical, Electronic Engineering Technology or Industrial Mechanics
Working experience in GMP, Medical Device, or Biotech Manufacturing regulated environment
Ability to use computer systems to support the material inventory system (SAP transactions) and electronic batch records
Excellent attention to detail, good organization, and capable of working independently

Job Responsibility

Perform equipment setup, operation, troubleshoot to meet all standards for safety, quality and efficiency
Maintain machine uptime, perform any fault clearing and clear stoppages on automated equipment
Perform basic, routine manufacturing process operations such as dispensing of raw materials, material reconciliation, line clearance, basic analytics, and record transactions
Assist in the review of documentation for assigned areas (i.e. procedures, job plans, logs, area audits and batch records)
Assist as training resource on manufacturing tasks and equipment use
Use human machine interfaces (HMIs) to identify alarms and correct line stoppages
Ensures components and products are available for a continuous operation
Carries out equipment inspections and generates emergency, corrective, or preventative work orders
Troubleshoot and identify potential solutions for mechanical errors, safety issues or general operating inefficiencies within the production processes
Partner with cross-functional teams to help drive improvement opportunities

What we offer

A comprehensive employee benefits package, including a Retirement and Savings Plan with generous company contributions, group medical, dental and vision coverage, life and disability insurance, and flexible spending accounts
A discretionary annual bonus program, or for field sales representatives, a sales-based incentive plan
Stock-based long-term incentives
Award-winning time-off plans
Flexible work models, including remote and hybrid work arrangements, where possible

Fulltime

Production Technician I

The technician will be responsible for assembling, operating, and monitoring sta...

Location

United States , Melrose Park

Salary:

24.00 USD / Hour

HonorVet Technologies

Expiration Date

Until further notice

Requirements

Have a minimum of a High School Diploma, GED, or equivalent education with one year of experience in a relevant work environment
Able to work 12hr shifts on a 2-2-3 schedule
Able to stand on concrete floors for an extended period of time
Able to lift up to 35 pounds by bending and lifting
Able to move heavy equipment and components as needed
Able to work with hazardous materials including antineoplastic products and raw materials that could lead to serious illness/injury
Able to wear required personal protective equipment (eye protection, safety shoes, gown, gloves)
Must be able to understand, speak, and write English in order to comply with necessary SOPs, SPECs, Job-specific training materials, GMPs, and other manuals

Job Responsibility

Assembling, operating, and monitoring state-of-the-art, aseptic equipment following applicable Standard Operating Procedures and current Good Manufacturing Practices
Practice good aseptic techniques to minimize the potential for product contamination
Understand advanced computerized systems through HMI
Ability to operate advanced HMI applications
Perform basic level machine operation, set-up and troubleshooting of all state-of-the-art equipment in their area
Load Parts Washer, Component Sterilizer, Vial Washer, Filling Machine and Capping Machine with raw materials and format parts
Maintains a down qualification if required by their area
Perform microbiological monitoring within the Filling Machine, ALUS, and Capping Machine
Assist other departments including MQA, Maintenance, Metrology, Engineering, Validation, Tech Transfer and Microbiology, with tasks on the equipment in their area General
Clean and sanitize equipment and Production areas per SOP

Fulltime

Maintenance Technician

The Maintenance Technician reports to the Manager, Maintenance Operations, and i...

Location

Ireland , Cork

Salary:

Not provided

BioMarin Pharmaceutical

Expiration Date

Until further notice

Requirements

A relevant third level qualification in Engineering or time-served apprenticeship
3+ years’ experience in a GMP environment, preferably Bio-pharmaceuticals or equivalent industry with drug product fill finishing and packaging activities

Job Responsibility

Proactively maintain process, utility and facility equipment in accordance with cGMP regulations, applicable safety considerations, Standard Operating Procedures, best maintenance practices and the reliability agenda
Maintenance and troubleshooting of drug product fill finishing line and packaging equipment
Interact with all process partners to continuously improve operations by recognising and correcting the causes of less than optimal equipment, facility and team performance
Manage external vendor support to complete required services in a GMP compliant manner
Perform problem solving including root cause analysis as required when equipment failures result in loss of production, substandard equipment performance and substantial repair cost and/or personnel safety incidents
Ensure Electrical, Process and Utility Systems are maintained in a controlled state thus ensuring compliance with all procedures and regulations and reliability initiatives
Maintain a safe working environment by continuously promoting safety awareness, recognising and rectifying unsafe conditions and performing thorough investigations when accidents occur
Record all maintenance work performed on the site CMMS system
Respond to critical utility alarms generated from the site automated alarm messenger system
Maintain documentation and management and control systems in compliance with cGMP regulations and training instructions

Fulltime

Validation Technician

The role of the "Validation Technician" with experience in performing Smoke Stud...

Location

Italy , Sabaudia

Salary:

Not provided

S.T.B. ValiTech S.r.l.

Expiration Date

Until further notice

Requirements

Diploma or degree in a technical/scientific field
At least one year of experience as a validation technician or in similar positions
Strong knowledge of regulations and quality standards (UNI EN ISO 14644-1, UNI EN ISO 14644-3, and EudraLex - Volume 4 Annex 1)
Proficiency in IT
Solid knowledge of videomaking
Familiarity with the following software: Blackmagic DaVinci Resolve and DJI Mimo
Experience with validation instrumentation – HVAC
Attention to detail and precision
Strong analytical and problem-solving skills
Good communication skills and a team-oriented attitude

Job Responsibility

Conduct Smoke Studies: Verify airflow patterns to ensure the proper movement of air within controlled contamination environments or installations
Video Recording and Editing: Plan, execute, and edit video recordings to document and analyze airflow and other validation activities
Qualification and Requalification of Pharmaceutical Systems: Perform qualification activities in compliance with current regulations and GMP (Good Manufacturing Practice Guidelines) requirements
Project Management: Coordinate and oversee testing, validation, and documentation phases, ensuring adherence to quality standards and deadlines
Collaboration with Various Operational Areas: Work closely with different teams to meet deadlines and ensure high-quality work while fostering a collaborative and efficient work environment
Validation Documentation Preparation: Draft comprehensive reports or protocols for qualification activities, ensuring traceability and compliance with current regulations
Compilation of Qualification and Requalification Reports: Compile reports and documentation by collecting data from qualification activities, including detailed documented evidence of tasks performed

What we offer

A stimulating growth path with leading clients in the pharmaceutical sector, providing opportunities for professional development in a dynamic and innovative environment

Compounding Technician

A Compounding Technician responsible for the aseptic production process, includi...

Location

Australia , Coorparoo

Salary:

Not provided

Baxter

Expiration Date

Until further notice

Requirements

Enjoy work that requires a high attention to detail
Willingness to learn new skills
Adapting to shift work schedules as needed
Providing assistance in environments with defined procedures and protocols
Knowledge of safety protocols and procedures to maintain a safe and efficient work environment
Be comfortable working within a cleanroom environment for most of your working day
Executing repetitive results in a consistent and accurate manner
Demonstrate a good understanding of basic mathematics
Communicate effectively both verbally and in writing
Experience in pharmacy, manufacturing or warehousing would be an advantage

Job Responsibility

Picking and preparing raw materials
Aseptically compounding (mixing) sterile solutions
Packing of finished units for each order including final inspection of products
Labelling and dispatching of prepared products
Ensuring documentation is completed in accordance with Good Manufacturing Practice (GMP)
Adhering to Baxter’s Standard Operating Procedures
Contribute to Baxter’s full inclusion and diversity culture
Other duties as required

What we offer

Full training provided
Recognition as an Employer of Choice for Gender Equality
Support structures for working families
Actions to address pay inequalities
Strategic recruitment and promotion practices for women
Equal opportunity employer

Fulltime

Manufacturing Process Technician

As part of Amgen’s Operations Organization, our Manufacturing Function continuou...

Location

Ireland , Dun Laoghaire

Salary:

Not provided

Amgen

Expiration Date

Until further notice

Requirements

Pass Leaving Certificate standard or equivalent
Minimum 12 months experience of operations within a sterile pharmaceutical manufacturing or similar environment OR Minimum 2 years of experience in a GMP and/or equivalent regulated environment
Demonstrated knowledge of GMP principles and aseptic knowledge within GMP areas
Drug product manufacturing experience
Experience working with equipment utilized in the manufacture of parenteral products such as autoclaves, filling lines and formulation vessels
Demonstrated understanding and use of Right First Time (RFT) techniques and lean manufacturing concepts
Demonstrated mechanical aptitude
Excellent problem-solving and communication skills
Experience working in Grade A/B area in Graded Aseptic Areas
Proactive and results-focused with excellent organizational skills

Job Responsibility

Set up of manufacturing equipment, processing of parts and components for manufacturing, performing transactions in electronic systems such as EBR, LIMS, etc. and cleaning and sanitization of production areas
Perform duties with due care and in accordance with Good Manufacturing Practices (GMP), Safety Regulations and Amgen requirements
Problem solving and troubleshooting, including initiation and documentation of investigations
Performance of self-inspection during Quality & Safety Audits
Support Corporate, FDA, IMB Auditors and other regulatory bodies during company audits
Participate in the learning and development program via the Maximizing Amgen Performance (MAP) process
Support cross functional training across team members
Ownership for the use, review, revision and upgrade of operational documentation and peer review of operations
Play a key role in the development of manufacturing systems
Proactively identify operational improvement and continuous improvement opportunities and / or process related issues including escalation & follow up for effective resolution and implementation

What we offer

Competitive salary structure
Generous Total Rewards Plan for staff and eligible dependents
Comprehensive employee benefits package, including retirement and savings plan with generous company contributions, group medical, life and disability insurance
Discretionary annual bonus program
Exceptional learning, development and career advancement opportunities

Fulltime

Manufacturing Process Technician

Be part of Amgen's newest and most advanced drug substance manufacturing plant. ...

Location

United States , Holly Springs

Salary:

57623.00 - 68426.00 USD / Year

Amgen

Expiration Date

Until further notice

Requirements

High school diploma / GED + 1 year of manufacturing and/or other regulated experience
Associate’s degree
Completion of NCBioWorks Certificate Program
Experience in a regulated industry such as biotechnology or pharmaceutical
Basic understanding of GMP principles
Strong verbal and written communication skills
Proficient Microsoft Office skills, and knowledge of other electronic systems such as EBR/MES, Delta V, and Electronic Quality Systems
Ability to perform assignments with a high degree of focus/attention to detail.

Job Responsibility

Completes work in accordance with established cGMP procedures and policies (Standard Operating Procedures [SOPs], Manufacturing Procedures [MPs], Job Hazard Analysis [JHAs], Code of Federal Regulations [CFR]) with strict adherence to safety and compliance
Documents accurately tasks performed and/or verified
Ensure proper gowning and aseptic techniques are always followed
Perform hands-on operation including set-up, cleaning, sanitization, monitoring of equipment in assigned area
Buffer and Media preparation and transfer
Complete washroom activities: cleaning equipment, small to large scale, used in production activities
Run and monitor critical processes per assigned procedures
Perform documentation for assigned function (i.e., equipment logs, EBRs)
Maintain an organized, clean, and workable space.

What we offer

Competitive and comprehensive Total Rewards Plans
Competitive benefits
Collaborative culture
Support for professional and personal growth and well-being.

Fulltime

Manufacturing Process Technician

Be part of Amgen's newest and most advanced drug substance manufacturing plant. ...

Location

United States , Holly Springs

Salary:

57623.00 - 68426.00 USD / Year

Amgen

Expiration Date

Until further notice

Requirements

High school diploma / GED + 1 year of manufacturing and/or other regulated experience
Associate’s degree

Job Responsibility

Completes work in accordance with established cGMP procedures and policies (Standard Operating Procedures [SOPs], Manufacturing Procedures [MPs], Job Hazard Analysis [JHAs], Code of Federal Regulations [CFR]) with strict adherence to safety and compliance
Ensure accurate gowning and aseptic techniques are always followed
Perform hands-on operation including set-up, cleaning, sanitization, monitoring of equipment in assigned area
Buffer and Media preparation and transfer
Weigh and dispense of materials to be used in the preparation of Buffers and Medias
Complete washroom activities: cleaning equipment, small to large scale, use in production activities
Run and monitor critical process per assigned procedures
Perform documentation for assigned function (i.e., equipment logs, EBRs)
Maintain an organized, clean, and workable space

What we offer

competitive and comprehensive Total Rewards Plans that are aligned with local industry standards

Fulltime

Manufacturing Technician- Pharmaceutical

SRG

Location:
United Kingdom , Stirling

Category:
Manufacturing

Contract Type:
Not provided

Salary:

Job Description:

Job Responsibility:

Requirements:

Nice to have:

Additional Information:

Job Posted:
February 18, 2026

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