Fill Finish operator Job at Beacon Hill (Concord)

Production Technician - Fill

The Fill Production Technician I is a Salaried Non-Exempt position which contrib...

Location

United States , Marion

Salary:

26400.00 USD / Year

Baxter

Expiration Date

Until further notice

Requirements

High School Diploma or GED and must be at least 18 years of age
CRC (Career Readiness Certification) at the Silver level preferred
Production Technician or manufacturing experience with duties including preventative maintenance, machine troubleshooting, etc. preferred
Basic English written and oral communication skills adequate to communicate with other team members
Understand verbal and written safety and quality instructions and read and comprehend written work instructions including words and drawings
Ability to perform basic mathematics
Proficient in how to use a calculator and measurement tools as well as basic hand tools
Basic computer skills

Job Responsibility

Operate, monitor and make adjustments as necessary to manual and automated filling equipment and machines using controls on an electrical control panel (HMI) or by way of manual adjustments
Set-up load and replenish production supplies by use of a powered industrial truck (PIT) at a rate consistent with production needs
Perform minor routine and preventative maintenance such as alignment adjustments, replacement of machine parts or belts, cleaning and lubrication while supporting Total Productive Maintenance (TPM)
Reconcile headcount needed on a per shift basis based on schedule production demands
Perform scheduled quality checks, disposition product, identify any deviations that may occur and take the appropriate action to include stopping production on the machine if necessary
Inspect finished product to ensure quality standards are being met
Execute Batch/Code changes, tank changes, as well as sub lots as required
Document required information on manufacturing logs and/or POMS system
Investigate, identify and correct or escalate any inefficiency in the machine’s performance including mechanical wear, alignment, adjustment, and setup issues
Develop standard work for troubleshooting and setups/changeovers

What we offer

Shift flexibility to trade shifts and leverage overtime opportunities
Medical, Dental and Vision coverage
160 hours of Paid Time Off and Paid Holidays
401K match
Employee Stock Purchase Program
Paid Parental Leave
Tuition Reimbursement

Parttime

Senior Director, Manufacturing, Science & Technology

As a Senior Director, Manufacturing, Science & Technology, you will lead a high-...

Location

United Kingdom , London

Salary:

Not provided

Theramex

Expiration Date

Until further notice

Requirements

PhD in Chemistry, Biochemical Engineering, or a related scientific discipline
Extensive experience in pharmaceutical or biotechnology manufacturing, with deep expertise in process development for both small and large molecules
Proven knowledge in sterile processing, fill-finish operations, and packaging
Strong understanding of CMC requirements and regulatory dossier submissions (EMA, FDA)
Inspirational leadership with a hands-on approach to managing technical operations, complex projects, and cross-functional teams
Exceptional analytical, scientific, and communication skills, with the ability to convey complex concepts to diverse stakeholders
Fluency in English is essential
Willingness to travel internationally as required

Job Responsibility

Provide strategic direction and technical oversight for all external manufacturing activities
Lead and oversee the execution of technology transfers, validation programs, and lifecycle management for both new and existing products
Establish and monitor performance metrics, proactively manage risks, and make data-driven decisions aligned with business objectives
Ensure robust technical evaluations for material changes, process scale adjustments, and cost-efficiency initiatives
Contribute to vendor qualification, audit processes, and long-term capacity and supply planning
Ensure full compliance with cGMP regulations and internal quality standards across all operations
Lead and manage a team of pharmaceutical technical and scientific experts
Serve as the primary technical liaison with CMOs, ensuring alignment with strategic goals and regulatory expectations

What we offer

A fast-paced environment, with broad exposure, where you can develop professionally – even outside your area of expertise
We support you as you grow and learn, and we love to celebrate success and recognize performance
We provide opportunities for driven and talented professionals who want to be part of our exciting journey

Production Specialist I

Diasorin is a global leader in diagnostic solutions, pushing the boundaries of s...

Location

United States , Stillwater, Minnesota

Salary:

18.24 - 22.53 USD / Hour

Diasorin

Expiration Date

Until further notice

Requirements

H.S. Diploma or equivalent and 1+ years manufacturing experience in related field required
Experience in biotechnology / medical device fields preferred
Ability to read, write and speak in English
Ability to use basic math functions in documentation process
Experience working with Microsoft Office programs
Attention to detail
Independently operate all machinery as assigned

Job Responsibility

Execute filling, filling support processes, and in-process quality control checks according to standard operation procedures
Maintain working knowledge of cGMP requirements to ensure adherence to company policies and procedures
Set up and operates filling equipment in clean room and non-clean room environments to produce work in process and finished components
Competent to complete cGMP filling documentation
Clean, prepare, and set-up production equipment for processing operations
Operate production equipment in clean room and non-clean room environment
Perform in-process quality checks for specific quality attributes (fill check, torque check and label check, etc.)
Inspect product for defects and conformance to quality standards
Clean work area and production equipment
Decontaminate work surfaces in accordance with defined procedures

What we offer

comprehensive plan of health benefits
retirement and financial wellbeing
time off programs
wellbeing support and perks
may be eligible to participate in an annual incentive program

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

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

Manufacturing Specialist – Process Owner (Syringe)

An exciting and rare opportunity has presented for a Site Fill Finish Process Le...

Location

Ireland , Dun Laoghaire

Salary:

Not provided

Amgen

Expiration Date

Until further notice

Requirements

Bachelor’s degree in Science, Engineering or related discipline with 10 + years’ experience in the pharmaceutical industry
Experience with regulatory compliance in cGMP manufacturing and in-depth knowledge of Eudralex Volume 4, Annex 1 Manufacture of Sterile Medicinal Products
Proven ability to work in a high paced matrix organization and effectively influence change and escalate issues professionally and in a timely manner
Excellent Decision-Making skills and confidence to respectfully and professionally challenge others on decisions that impact the manufacturing area
Proactive and works well with others in a collaborative, fast-paced goal-driven environment
Interacts well with diverse groups (Manufacturing, Validation, Engineering, Quality etc) and maintains strong working relationships with internal and external collaborators
Demonstrated ability to coach, mentor and/or cross train colleagues within core technical areas
Excellent verbal and written communication skills: Strong Technical writing skills for cGxP documentation (eg investigations, procedures, change controls) and good Presentation skills

Job Responsibility

Perform as a knowledgeable subject matter expert (SME), and single point of contact on site and network projects and programs, to advance Fill Finish manufacturing operations
Leading and/or providing input to strategic initiatives that will improve and develop processes for the future
Contribute in a team environment to operational issues pertaining to processes as they arise and provide expertise and support to help resolve escalated technical issues as required
Utilise subject matter expertise to identify and lead continuous improvement projects in assigned area of responsibility. Ensure project timelines are met, challenges identified, mitigations are in place and communication plans delivered to all stakeholders
Involved in the daily business management systems and reporting, have a clear understanding of what is happening in the assigned area of responsibility. Monitor any process trends including business performance metrics. Identify actions that will enable the process and the Manufacturing areas better achieve and surpass metrics in the future
Lead and/or Support investigations that impact on safety, quality and/or compliance of the processes, ensuring thorough investigations are carried out and actionable CAPAs, to prevent future reoccurrence, are identified and implemented within agreed timeline
Remain current on state-of-the-art for systems and processes and advise on the appropriate adoption and use of new techniques and technology

Inbound Forklift Operator

This role operates and maintains equipment associated with warehouse activity an...

Location

United States , Broussard

Salary:

Not provided

Sysco

Expiration Date

Until further notice

Requirements

2 years of warehouse experience
Pass mandatory ergonomics testing
Working knowledge of Sysco safety and security policies, equipment associated with warehouse activities and the operation of the equipment
Demonstrated ability to disseminate numerical data
Manage work time efficiently
Follow procedures and policies
Perform basic mathematical calculations
Identify and solve problems
Must be able to manage the pressures and stress associated with a deadline-oriented atmosphere
Possess excellent interpersonal and communication skills

Job Responsibility

Responsible for the storage and movement of materials and finished goods including: Shipping and receiving
Warehousing
Order filling
Operates and maintains equipment associated with warehouse activity
Control flow of products being received into the warehouse
Conform to appropriate equipment (i.e., tugs, forklifts, pallet jacks) operation rules and practices to reduce accidents and injuries
Guarantee that assigned equipment is maintained and clean
report repair or service needs to the manager to reduce equipment damage
Observe all safety rules, regulations, and sanitation policies to reduce accidents, injuries, and equipment damage
Use equipment horns when driving out of storage areas, into obstructed view areas, and when entering walkways or row intersections to reduce accidents, injuries, and equipment damage

Fulltime

New

Specialist Furniture Sprayer

A skilled professional who prepares and finishes premium furniture using both po...

Location

Netherlands , Schijndel

Salary:

Not provided

Fareon Nederland B.V.

Expiration Date

Until further notice

Requirements

An education at mid-level, preferably in shipbuilding
Possession of a valid VCA or VCA-Vol certificate
Must be able to communicate with the employee in Dutch or English
Demonstrable work experience as a Ship Metal Worker
Experience with reading drawings, measuring and marking
Experience with tack welding, grinding and burning
Experience with spray finishing techniques, including powder coating and wet-lacquering
Surface preparation: sanding, degreasing, filling, and masking
Finishing and polishing: inter-layer sanding, buffing, and gloss control
Color and gloss accuracy: precise color matching and finishing on high-end furniture

Job Responsibility

Prepares and finishes premium furniture using both powder coating and wet-lacquering techniques
Ensures flawless surfaces, precise color matching, and perfect gloss, working on high-end designer pieces
Strong focus on craftsmanship, attention to detail, and quality control in a clean, controlled environment

What we offer

Monthly vacation allowance of approximately 130 EUR
Health care contribution of approximately 120 EUR per month
Transportation allowance of 0.19 EUR/km for commuting with own vehicle
Accommodation provided in a private room with shared facilities
Weekly payment
Dutch employment contract, including pension contributions and holiday allowance
Long-term employment where craftsmanship is highly valued
Pleasant working atmosphere

Fulltime

Fill Finish operator

Beacon Hill

Location:
United States , Concord

Category:
Manufacturing

Contract Type:
Not provided

Salary:

Job Description:

Job Responsibility:

Requirements:

Nice to have:

Additional Information:

Job Posted:
December 24, 2025

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Fill Finish operator

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Location:United States , Concord

Category:Manufacturing

Contract Type:Not provided

Salary:

Job Description:

Job Responsibility:

Requirements:

Nice to have:

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Job Posted:December 24, 2025

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