Referso Jobs

Manufacturing Process Technician (12hr AM)

Amgen · Posted Nov 9, 2026

Open

New Albany, Ohio, United States
$54K–$74K per year
1+ years

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Manufacturing Process Technician (12hr AM)

Amgen · Posted Nov 9, 2026

Open

New Albany, Ohio, United States
$54K–$74K per year
1+ years

Apply with Referso

Manager Packaging

New Belgium Brewing · Posted Nov 9, 2026

Open

Daleville, Virginia, United States
On-site
Full-time · Manager
$90K–$105K per year
7+ years

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Responsible for overall performance of the packaging department, including people, equipment, and systems, driving continuous improvement for optimal production performance.

Compensation

Starting Salary: $90,000-$105,000

Responsibilities

Oversee packaging department and initiatives; direct and coordinate production processes and operational functions to achieve goals and optimal production performance; meet production schedules and quality standards; coordinate with distribution to ensure efficiency between departments.
Monitor and recommend improvements in processes to increase efficiency; support quality efforts, coordinate teams to resolve quality problems and develop resolutions; sponsor yearly vendor audits; prepare, prioritize, and justify project resource requests
Develop and drive productivity strategies designed to promote continuous improvement efforts and optimize production efficiencies; utilize tools such as 6s, TPM, TAKT, value stream mapping, etc.; analyze, and measure cost and impact of productivity initiatives
Manage and coach leadership team, mentor and develop leadership skills, monitor department coherence, conduct performance reviews, and develop succession plans
Maintain and ensure safety compliance including overseeing safety standards and policies are followed and manage safety concerns and continuous improvement efforts.

Requirements

Quality Engineer I

Freudenberg Group · Posted Nov 9, 2026

Open

Beverly, Massachusetts, United States
0–3 years

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Compensation

Compensation for this position will be determined by the candidate's qualifications, experience, education, and overall alignment with the role's responsibilities.

Responsibilities

Understand quality system requirements to support the development, qualification and manufacturing of products to meet internal and external requirements.
Utilize statistical analysis tools to support project team.
Support creation of Master Validation Plan, validation protocols and reports (IQ/OQ/PQ), quality design reviews deliverables, risk management plan, and all quality related documentation.
Assist in and may lead supporting nonconformances, complaints, CAPAs, etc. to resolve quality issues.
Support internal and external audits, ensuring quality system compliance.

Requirements

Bachelor's/University degree in Engineering, Chemistry, Biology, or related science/technical field.

Skills

statistical methods process control Design of Experiments (DOE)Failure Mode and Effects Analysis (FMEA)

Bioprocess Technician

Amgen · Posted Nov 9, 2026

Open

Dublin, Leinster, Ireland
€39K–€53K per year
12+ years

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Bioprocess Technician responsible for manufacturing sterile parenteral drugs at Amgen’s manufacturing site.

Compensation

Salary Range 39,477.40 EUR - 53,410.60 EUR

Responsibilities

Set up manufacturing equipment
Process parts and components for manufacturing
Perform transactions in electronic systems such as EBR, LIMS
Clean and sanitize production areas
Perform duties in accordance with GMP, safety regulations and Amgen requirements

Requirements

Pass Leaving Certificate standard or equivalent
Third level qualification in a relevant subject area (preferred)
Nice to have: Third level qualification in a relevant subject area

Skills

GMP principles Aseptic knowledge within GMP areas Drug product manufacturing experience Experience with equipment used in manufacture of parenteral products such as autoclaves, filling lines and formulation vessels

GMP Stockroom Technician

SBM Management Services, LP (SBM Site Services LLC) · Posted Jun 25, 2026

Open

Vacaville, California, United States
On-site
Full-time · Entry
$22–$23 per hour
0–1 years

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The GMP Stockroom Technician is responsible for the proper handling, storage, and distribution of materials, including consumables, chemicals, personal protective equipment (PPE), and other essential supplies for both GMP and non-GMP areas within the facility.

Compensation

$22.00-$23.00 per hour

Responsibilities

Clean, maintain, and organize all stock locations.
Compile reports on use of stock handling equipment, adjustments of inventory counts and stock records, spoilage of or damage to stock, location changes, and refusal of shipments.
Adhere to all GMP, safety, and environmental policies and procedures.
Ensure proper material transfer by following decontamination procedures and unidirectional flow when moving items from non-classified to classified areas.
Adhere to gowning protocols to prevent cross-contamination when entering classified spaces.

Requirements

High School Diploma / GED
Nice to have: CPR/AED/First Aid certification
Nice to have: valid driver’s license
Nice to have: forklift certified

Skills

GMP principles cleanroom environments contamination control protocols

Manufacturing Process Technician - West Greenwich RI

VetJobs · Posted Nov 4, 2026

Open

West Greenwich, Rhode Island, United States
On-site
$54K–$74K per year
1+ years

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Manufacturing Process Technician - Days

Compensation

54,411.05USD -73,614.95 USD

Responsibilities

Equipment and parts cleaning using manual and automated methods and equipment
Set up and breakdown of single use materials
Weigh and dispense of raw materials
Operation and process monitoring of clean systems, autoclaves, and processing equipment
Sample collection, processing, storage and delivery

Requirements

High school/GED + 1 year of Manufacturing or Operations work or military experience
Associate's degree
Nice to have: Experience in a GMP/other regulated environment
Nice to have: Demonstrated knowledge of GMP principles
Nice to have: Drug substance manufacturing experience

Skills

Manufacturing or Operations work GMP principles Drug substance manufacturing Stand or sit for extended periods Maintain focus during repetitious tasks

QA Expert Audits and Inspections 80-100%

Lonza · Posted Nov 4, 2026

Open

Stein, Aargau, Switzerland
Hybrid

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Coordinate and support audits and inspections at a sterile filling manufacturing site, ensuring compliance and quality management.

Responsibilities

Coordinate and support regulatory inspections and customer audits
Act as a key back‑office partner during audits and inspections
Drive audit and inspection follow‑up activities in TrackWise
Contribute to inspection readiness initiatives
Support GMP compliance and Quality Management System activities

Requirements

Bachelor's or Master's degree in Life Sciences or a related field
Nice to have: German language proficiency

Skills

GMP principles quality processes compliance requirements sterile manufacturing or biologics/drug substance operations customer audit and/or regulatory inspection experience

See full job description

Project Engineer

PM Group · Posted Nov 4, 2026

Open

Dublin, Leinster, Ireland
On-site
Full-time · Mid
5+ years

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A Project Engineer focused on GMP Manufacturing and Utilities supporting the delivery of strategic capital projects within a pharmaceutical manufacturing environment.

Responsibilities

Support and deliver projects throughout the full project lifecycle, from concept and design through commissioning, qualification, and handover
Lead or support cross-functional teams delivering manufacturing, process, facility, and utility-related projects in a highly automated GMP environment
Provide technical expertise in utilities, ideally GMP clean utilities, acting as a System Owner or Project Engineer where required
Manage project scope, schedules, budgets, contractors, vendors, risks, and mitigation plans
Support project financial performance, including forecasting, cost control, risk assessment, and lifecycle cost considerations

Requirements

Degree (Level 8 preferred) in Engineering, Science, or a related discipline

Skills

GMP manufacturing Project Engineering clean utility systems project lifecycle

IT Lab Computing Support Specialist

Artech LLC · Posted Nov 2, 2026

Open

Bothell, Washington, United States
On-site
Full-time · Associate
$39–$50 per hour

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Provide senior-level technical support and ownership for GMP laboratory computing systems and associated services.

Compensation

Pay Range: $39.07/hr - $49.62/hr

Responsibilities

Provide senior-level technical support and ownership for GMP laboratory computing systems and associated services.
Maintain reliable operation of laboratory applications, computerized systems, workstations, instruments, interfaces, and supporting infrastructure.
Serve as a technical subject matter expert for assigned laboratory computing platforms and services.
Lead troubleshooting of complex technical issues and coordinate resolution across multiple technical and business teams.
Provide technical direction during system incidents, service interruptions, and complex operational events.

Requirements

Bachelor’s degree in computer science, Computer Engineering, Electrical Engineering, Information Technology, Life Sciences, or related technical discipline
Nice to have: pharmaceutical
Nice to have: biotechnology
Nice to have: medical device
Nice to have: highly regulated laboratory environments

Skills

laboratory computing GMP-regulated environment

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