Manufacturing Operator

We are seeking Manufacturing Operators for an exciting 6-month fixed-term contra...

Location

New Zealand , Auckland

Salary:

Not provided

Argenta

Expiration Date

Until further notice

Requirements

Proven experience in production or manufacturing within a GMP environment, with a strong emphasis on quality and adherence to SOPs
Solid understanding of Health & Safety practices and a demonstrated commitment to maintaining a safe workplace
Minimum of 3 years of manufacturing experience in pharmaceutical, animal health, food, or a related industry
Excellent written and verbal communication skills to collaborate effectively within teams
A natural mechanical aptitude and problem-solving mindset
Physical fitness is beneficial for this role, including the ability to safely handle items weighing up to 25kg as part of daily operations
Must have the right to work in New Zealand

Job Responsibility

Be competent in manufacturing and packaging operations for Solid Dose and Liquids, including operating assembly, packing and labelling equipment and performing in-process quality checks
Troubleshooting mechanical problems and providing feedback to Engineers
Maintaining a high level of housekeeping and cleanliness within the production area
Ensuring all equipment used is cleaned, calibrated and lubricated between batches
Production batch documentation is completed accurately and in compliance to cGMP standards
Compliance to Health & Safety at all times

What we offer

Competitive hourly rate and generous allowances
Comprehensive insurance cover
Access to EAP support
Fresh fruit every week
Regular on-site events

Fulltime

New

Contract Manufacturing Director

As Contract Manufacturing Director you will be responsible for the strategic and...

Location

United Kingdom , Swindon

Salary:

101700.00 - 155100.00 GBP / Year

BD

Expiration Date

Until further notice

Requirements

A minimum of 10 years of experience in the pharmaceutical, medical devices, automotive or consumer goods industry
At least 5 years of direct experience in external/contract manufacturing
Proven leadership in managing CMOs across multiple geographies and technologies, including (but not limited to) sterile manufacturing, oral solid dose, biologics, active pharmaceutical ingredients (API), and packaging
Strategic Vision: Ability to shape external manufacturing networks and anticipate risks
Technical Depth: Solid grasp of manufacturing technologies, quality, and regulatory standards
Influence & Negotiation: Skilled in leading without authority and managing external partners
Analytical Thinking: Strong problem-solving and data-driven decision-making
Operational Rigor: Proven track record in planning, execution, and performance management
Collaborative Leadership: Effective in matrixed, cross-functional environments
Business Insight: Understanding of cost drivers, contracts, and financial levers

Job Responsibility

CMO Governance & Performance Management: Lead the relationship with assigned CMOs, ensuring strong operational performance and continuous improvement
Establish and oversee governance structures
Monitor key metrics
Lead issue escalation, resolution pathways, and structured problem-solving with CMO partners
External Manufacturing Strategy: Develop and execute the external manufacturing strategy for assigned product portfolio
Assess capabilities, risks, and opportunities across the CMO landscape
Contribute to make/buy decisions, outsourcing strategies, and network optimization initiatives
Support business case development for transferring products to new CMOs or scaling capacity
Operational Excellence & Cost Management: Drive productivity programs and cost‑reduction initiatives across the external network
Ensure robust demand planning, capacity planning, and inventory strategies with CMOs

Fulltime

Senior Process Engineer

Location

Canada , Mississauga

Salary:

Not provided

Advanced Technology Search Group

Expiration Date

Until further notice

Requirements

Minimum 10 years’ experience in leading the design/construction of capital and CI projects in a fast paced, high-technology, team environment, preferably in the pharmaceutical or food industry, with at least of 3 years in leadership experience
In depth technical understanding of relevant unit operations in the pharmaceutical industry, their capabilities and associated processes. High preference for liquid and semi-solid dose operations
Proven track record in managing major capital and CI projects in a team environment “on time and on budget”
In depth understanding of automated / integrated production equipment and computerized systems
In depth knowledge in the qualification and validation of equipment, facility and processes. Proficiency in the creation of qualification documentation with minimal supervision
Experience in managing customers, vendors, consultants and contractors
Proven leadership capabilities/competencies, and ability to manage teams and reach objectives without formal reporting relationships
Knowledgeable in the numerous regulatory aspects of capital construction, including the Occupational Health and Safety Act, the Ontario Building Code, the Boiler and Pressure Vessel Act, etc.
PEO (Professional Engineer of Ontario) designation eligibility - P. Eng. preferred

Job Responsibility

Working with members of the Engineering Team, assemble the appropriate project team to execute each project through concept development, scope definition and estimating, design, and construction execution. An important part of this role is the understanding of the end user requirements through ongoing consultation with representatives of those customer groups
Use mechanical, electrical and/or process systems expertise to work with individual Project Delivery Teams to ensure the appropriate commissioning, qualification and training plans with accompanying resources are in place to deliver efficient system start-up
In cooperation with other project leadership team members, ensure that all systems are in place to ensure due diligence in design and construction procurement/execution and project cost and schedule controls
Ensure that all work is performed in full compliance with established regulatory standards including, but not limited to, company safety policies and procedures, cGMP, building code and MOL/MOE requirements
Lead the development and ongoing maintenance of engineering design and construction standards and ensure compliance on all project executions
Support as required the trouble-shooting and problem resolution of facility systems and operational equipment
Ensure all necessary permits, as required by the current codes, are obtained and that any necessary inspections are scheduled
Lead and support the development and execution of F.A.T-, commissioning and validation requirements and associated documentation for work assigned, as required
Actively supports the Business Development (BD) team in the introduction of new products and modifications of existing products. Provide technical support to BD on creation of new routing and provide process flows for the manufacturing and packaging of new products and/or modification of existing products
Leads customer process optimization and investigations, equipment selection and customer audits and visits

Fulltime

New

Packaging Technology Specialist

We manufacture and supply reliable, high‑quality medicines to meet patients’ nee...

Location

United States , Durham, North Carolina; Rockville, Maryland; Waltham, Massachusetts; Philadelphia, Pennsylvania

Salary:

111375.00 - 185625.00 USD / Year

GSK

Expiration Date

Until further notice

Requirements

Bachelor’s degree in
5+ years of experience in pharmaceutical packaging development, packaging equipment or packaging operations across multiple dose forms (e.g., solid orals, liquids, dermal, parenteral)

Job Responsibility

Lead development and introduction of first‑intent primary packaging for NPIs in the Medicines portfolio at External Manufacturing Sites
Provide packaging technology support to ensure NPI project milestones and launch dates are met
Define and deliver primary, secondary, tertiary and distribution pack designs: agree pack design briefs, evaluate design options, and ensure suitability for commercial, regulatory and manufacturing requirements
Collaborate with suppliers on component design, material selection, printing/conversion methods, cost and sustainability opportunities
Define and manage packaging functional testing (component interaction, child resistance, distribution performance, metrology) and technical review of test data and specifications
Support Packaging Validation and Production groups on equipment selection, machine trials, process qualification and control strategies to ensure robust, consistent processes
Assess and qualify packaging components, suppliers and supplier change proposals
partner with Procurement and Supplier Quality on supplier evaluations and lifecycle changes
Manage bulk packaging shipping lane qualifications and assessments for NPIs and project transfers
Identify and drive packaging improvements to reduce complexity, cost and waste while maintaining quality and compliance

What we offer

Competitive base salary
Annual bonus based on company performance
Flexible working options available for most roles
Learning and career development
Access to healthcare & wellbeing programmes
Employee recognition programmes
Eligibility to participate in our share based long term incentive program
Health care and other insurance benefits (for employee and family)
Retirement benefits
Paid holidays

Fulltime

MSAT Associate Director

Proclinical is seeking an MSAT Associate Director to oversee the successful tran...

Location

United Kingdom , Surrey

Salary:

Not provided

Proclinical

Expiration Date

Until further notice

Requirements

Degree in Life Sciences, Pharmacy, Pharmaceutical Sciences, or Chemistry
Proven experience in site-to-site technical transfers and pharmaceutical manufacturing processes
Familiarity with small molecule formats, including sterile products, capsules, creams, gels, ointments, and solid dose
Knowledge of Quality Management Systems, including change control and deviation management
Experience in operational budget management and strategic alignment
Proficiency in project management tools, templates, and methodologies
Strong problem-solving skills and ability to adapt to high-speed changes
Excellent organizational, communication, and time management skills
Demonstrated leadership and collaboration abilities across global teams
Commitment to continuous improvement and ethical standards

Job Responsibility

Ensure adherence to GxP regulations and standard operating procedures
Lead technical transfers of manufacturing processes, providing critical expertise and direction
Establish and track KPIs, budgets, and timelines for process transfers and improvements
Represent technical expertise in cross-functional projects, including supply chain, regulatory, and commercial activities
Provide scientific advice to procurement and regulatory teams, addressing batch failures, recalls, and variations
Conduct technical reviews and due diligence for potential acquisitions and divestments
Collaborate with manufacturing sites to optimize processes and resolve compliance or quality issues
Review and approve technical documentation, including certificates of analysis, stability data, and risk assessments
Manage quality records such as change control requests and deviations
Propose and implement technical and business improvements to enhance practices and systems

Fulltime

Sr. Team Leader - Equipment Maintenance

The Engineering Shift Lead for the IMA Filling Line is responsible for leading t...

Location

India , Vizag

Salary:

Not provided

Pfizer

Expiration Date

Until further notice

Requirements

Diploma (or equivalent) with 10+ years of experience or associate’s degree with 8+ years of experience or BA/BS with 5+ years of experience or MBA/MS with any years of relevant experience
Strong expertise in equipment and project management
Demonstrated direct supervisory experience
Solid understanding of knowledge management
Proficiency in Good Manufacturing Practices (including cGMP), OSHA, FDA, and environmental regulations relevant to the pharmaceutical industry
Strong English speaking and writing abilities

Job Responsibility

Lead mechanical/Instrumentation troubleshooting of IMA filling line equipment (e.g., sensors, PLC, conveyors, dosing units, sealing systems, servo mechanisms)
Ensure minimum downtime by providing quick and effective diagnostic responses to mechanical failures
Guide team members on root cause analysis, FMEA and corrective actions
Oversee execution of shift-level preventive maintenance (PM) activities as per schedule
Ensure proper lubrication, alignment, precision adjustments, and mechanical integrity checks
Identify recurring issues and propose reliability improvements
Lead and supervise a team of Team members and operators during the shift
Coordinate with Manufacturing, quality, safety, and warehouse teams to ensure smooth operations
Conduct shift handover meetings with accurate reporting of issues, breakdowns, and follow-up actions
Drive improvements in line efficiency (OEE), waste reduction, and equipment performance

Fulltime

New

Sales associate

Our Sales Associates help our customers Celebrate Life & Express Love! Our store...

Location

Isle of Man , Douglas

Salary:

12.25 GBP / Hour

Ernest Jones

Expiration Date

April 05, 2026

Requirements

Passion for putting the customer first and creating memorable customer experiences
Interest in jewellery products and brands
Positive, 'can-do' attitude
Natural ability for striking up a conversation with a diverse range of customers

Job Responsibility

Help customers Celebrate Life & Express Love
Provide outstanding service and create amazing experiences for customers
Develop outstanding product knowledge and jewellery expertise to share with customers
Help the store maintain performance and meet sales targets
Build knowledge on new products to deal with every type of customer enquiry
Reflect the H. Samuel brand, culture and customers

What we offer

Bonuses
Staff discount
Sales incentives
Career development opportunities
Training and development programmes

Parttime

New

Executive Chef

The Executive Chef is responsible for all culinary operations of multiple restau...

Location

United States , Sacramento

Salary:

92243.00 - 111809.00 USD / Year

HMSHost

Expiration Date

Until further notice

Requirements

Post-secondary, culinary arts school or four-year university
Minimum of 5 years managerial or supervision experience in the culinary/food service
Certified in Serve Safe Management certification course
Demonstrates team management, delegation, issue resolution, coaching skills and ability to motivate others and act as a change agent
Demonstrates organization and multi-project time/issue management
Ability to speak, read and comprehend instructions, short correspondence and policy documents, as well as converse comfortably with individuals

Job Responsibility

Supervises the day to day activities of culinary supervisory staff
Works with Restaurant partners on menus and menu items, ensuring that they can be prepared properly and timely in the airport kitchens
Ensures integrity of all aspects of food, i.e. taste, temperature, presentation, speed of production
Promotes safety and sanitation, oversees inspection of products handling, establishes and maintains safe practices, and follows HACCP procedures
Oversees the Commissary and serves as a primary contact with food vendors
Prices and orders food and kitchen supplies
Maintains effective cost control, by managing the food management inventory system
Complies with company and franchise standards of operation procedures, as well as those of all applicable regulatory agencies
Ensures on a daily basis that all products are prepared and presented in accordance with brand or company standards
Identifies hiring, firing, advancement, development, promotion of culinary management staff

What we offer

Health, dental and vision insurance
Generous paid time off (vacation, flex or sick)
Holiday pay
Meal and Transportation Benefits
401(k) retirement plan with company match
Company paid life insurance
Tuition reimbursement
Employee assistance program
Training and exciting career growth opportunities
Referral program – refer a friend and earn a bonus

Fulltime

Manufacturing Operator - Solid Dose

Fagron

Location:
United States , Spring Valley

Category:
Manufacturing

Contract Type:
Not provided

Salary:

Job Description:

Job Responsibility:

Requirements:

Additional Information:

Job Posted:
March 21, 2026

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